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Job Title	City	State	Posted on
International Partnership for Microbicides, Inc.	Silver Spring	MD	9/9/2010
Sr Financial Systems Analyst
Education/Experience: �?� Bachelor�??s Degree in accounting/finance or business. �?� A minimum of eight (8) years experience ideally gained through increasingly responsible positions within Finance including financial analysis and accounting. �?� Previous non-profit and Donor reporting experience is a plus. �?� Proficiency in one of the following or similar accounting software packages: Solomon, Great Plains, Deltek, People Soft. �?� Prior training or teaching experience. Knowledge, Skills, and Abilities: �?� Working knowledge of financial reporting systems. �?� High degree of proficiency with MS Office, particularly Excel. �?� Knowledge of accounting procedures and internal control processes. �?� Ability to understand, analyze, and explain financial information. �?� Ability to research problems and present solutions and alternatives. Timely and effective problem solver. �?� Good verbal and written communication skills. Ability to respond in clear and concise manner to requests and questions. �?� Strong self-management skills. Ability to set well-defined and realistic goals; monitor progress and achieve results; manage own time and deal with stress effectively; manage multiple tasks and projects. Ability to plan work in accordance with general direction. �?� Strong results orientation, i.e., the ability to work at a fast pace and meet critical deadline. �?� Ability to manage multiple projects, goals and deadlines. �?� Attentive to detail and accuracy. Thorough when performing work and conscientious about attending detail. �?� Commitment to the delivery of excellent customer service �?? works and communicated with internal and external clients to satisfy their expectations. Committed to quality service. �?� Ability to understand and control confidential information with absolute discretion. �?� Team player with excellent interpersonal communication skills. �?� Tolerant of some ambiguity; work well under pressure; assertive; and well organized. �?� A sense of humor, flexibility and humility. Position located at the Headquarters in Silver Spring, MD. Job holder should expect fast-paced working environment. Some international travel will be required.
International Partnership for Microbicides, Inc.	Silver Spring	MD	9/9/2010
Executive Assistant
Education and Experience �?� Bachelor�??s degree in business or related field highly desirable. �?� Minimum seven years assisting senior level executives (preferable C-level) in positions that required maturity, poise, ability to handle highly confidential and sensitive information. �?� Solid experience in communicating with high level stakeholders and constituents required. �?� Experience in HR and/or legal environments helpful. Knowledge, Skills and Abilities �?� Outstanding time management and organization skills. Ability to multi-task, assess priorities and competently handle a variety of activities with a high-degree of accuracy. �?� Advanced skills in Microsoft Office software applications (Outlook, Word, Excel and PowerPoint), web-based research and information collection, are essential. �?� Excellent communication skills, both verbal and written, for internal and external communications. �?� Ability to work and communicate with staff, consultants and other stakeholders through a variety of means to satisfy and address their expectations. �?� Committed to quality service. �?� Results oriented �?? able to work in a fast-paced environment and meet deadlines with competing priorities. �?� Adept at archiving, organizing and retrieving material effectively. �?� Strong ability to proofread and edit written material for sense, order and the correct use of grammar and punctuation. �?� Superior attention to detail and conscientious about accuracy of work product. �?� Highest level of confidentiality and professionalism required. Must be circumspect, tactful and diplomatic in all interactions. �?� Tolerant of some ambiguity; work well under pressure; assertive, yet respectful. Position is located in Silver Spring Maryland. IPM is an Equal Employment Opportunity employer.
International Partnership for Microbicides, Inc.	Silver Spring	MD	9/9/2010
Controller
Education/Experience: �?� Bachelor�??s Degree in accounting/finance or business and a CPA, CFA or other professional designation preferred. �?� A minimum of eight (8) years experience ideally gained through increasingly responsible position within Finance including accounting, auditing, and/or financial analysis. A minimum of two (2) years experience in accounting operations, which included a deadline-oriented closing process. �?� Experience with not-for-profit accounting and small-company accounting environments. �?� Experience in an international environment. Knowledge, Skills, and Abilities: �?� Working knowledge of financial reporting systems. �?� High degree of proficiency with MS Office, particularly Excel. �?� Knowledge of accounting procedures and internal control processes. �?� Knowledge of OMB and FAR. �?� Ability to understand, analyze, and explain financial information. �?� Ability to research problems and present solutions and alternatives. Timely and effective problem solver. �?� Good verbal and written communication skills. Ability to respond in clear and concise manner to requests and questions. �?� Strong self-management skills. Ability to set well-defined and realistic goals; monitor progress and achieve results; manage own time and deal with stress effectively; manage multiple tasks and projects. Ability to plan work in accordance with general direction. �?� Strong results orientation, i.e., the ability to work at a fast pace and meet critical deadline. �?� Ability to manage multiple projects, goals and deadlines. �?� Attentive to detail and accuracy. Thorough when performing work and conscientious about attending detail. �?� Commitment to the delivery of excellent customer service �?? works and communicated with internal and external clients to satisfy their expectations. Committed to quality service. �?� Ability to understand and control confidential information with absolute discretion. �?� Team player, sense of humor, and excellent interpersonal communication skills. �?� Tolerant of some ambiguity; work well under pressure; assertive; and well organized. Position located at the Headquarters in Silver Spring, MD. Job holder should expect fast-paced working environment.
International Partnership for Microbicides, Inc.	Silver Spring	MD	9/9/2010
Contracts and Grants Coordinator
Candidates for this position should have the following education/experience and demonstrate mastery of the following knowledge, skills, and abilities: Education/Experience College degree or equivalent years of experience working with contracts or with related administrative experience. Knowledge, Skills, and Abilities �?� Proficient in Excel and other Microsoft applications. �?� Experience working with finance or accounting tracking. �?� Good organizational skills; proven ability to prioritize projects and initiate follow through with meticulous attention to detail and high-level accuracy. �?� Ability to work effectively under pressure and handle multiple simultaneous tasks and demands. �?� Good interpersonal skills; tact, patience, diplomacy, and appropriate assertiveness. �?� Self-starter with ability to work independently and part of a team. �?� Ability to interpret and explain complex issues and identify those with financial implications �?� USAID experience preferred but not required Position located at Headquarters in Silver Spring, MD. Job holder should expect fast-paced working environment.
International Partnership for Microbicides, Inc.		Paarl	9/9/2010
Clinical Regulatory Officer
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily: EDUCATION AND EXPERIENCE �?�Bachelor�??s degree in life science or healthcare field, or equivalent. �?�Minimum of 3 years clinical research experience. �?�Minimum 2 year�??s experience with preparation of clinical trial submissions. �?�Previous GCP certification is an advantage. �?�Familiarity with Regulatory Agencies in Africa research settings is desirable. �?�Valid drivers�?? license. KNOWLEDGE, SKILLS AND ABILITIES �?�Ability to organize and prioritize multiple projects and tasks. �?�English verbal and written skills are required. �?�Ability to work independently and in a cross-functional team environment. �?�Attention to detail and timelines is critical. �?�Good understanding of document management. �?�Understanding of stakeholder management is an advantage. �?�Good conflict resolution and problem solving skills. �?�End-user computer efficiency, with proficiency in Microsoft Office products. Results orientation - ability to work in a fast-paced environment and meet deadlines with competing priorities. This position is based in the Clinical Affairs Department in South Africa IPM office. Job holder should expect fast-paced working environment. A valid driver�??s license as well as own reliable transport is required.IPM is an Equal Employment Opportunity employer.This job description should not be construed to imply that these requirements are the only standards for the position. Other duties will be assigned. IPM has the right to revise this job description at any time. IPM is an �??at will�?� employer and as such, neither this job description nor your signature constitutes any form of contractual arrangement between you and IPM.
International Partnership for Microbicides, Inc.		Paarl	9/9/2010
Associate/Director of Regulatory Affairs, Africa
Education and Experience �?� Minimum of seven (7) years of related experience with three (3) of those in a management capacity �?� Experience with pan-African regulatory policy and procedures and global regulatory policy and procedures �?� Education and experience equivalent to a Bachelor's Degree in public health, microbiology, clinical science or material science disciplines. Knowledge, Skills and Abilities �?� Creative, constructive, responsive approaches to the challenges of complex regulatory issue, particularly as related to African countries �?� Ability to work in a fast-paced environment and meet deadlines with competing priorities �?� Strong organizational skills with a high level of initiative, creativity, and assertiveness �?� Clear, concise, effective verbal (technical and interpersonal) and written (administrative and technical) communication �?� Excellent organizational, planning, negotiating, and problem-solving skills �?� Cultural sensitivity �?� Ability to lead and participate on teams within IPM to interact effectively with regulatory agencies, clients, colleagues, supervisors, subordinates, and the public Employee should expect a fast-paced working environment. Willingness to travel as needed. IPM is an Equal Employment Opportunity employer.
International Partnership for Microbicides, Inc.		Paarl	9/9/2010
Associate Director of Clinical QA
Education/Experience �?� Bachelor�??s or Master�??s degree in biology, chemistry or related field �?� Approximately 8-10 years experience in quality assurance with demonstrated expertise in Good Clinical Practice regulations and guidelines �?� Experience with supervision of quality assurance professionals Knowledge, Skills and Abilities �?� Excellent written and oral communication skills �?� Experience working with external contractors and consultants �?� Strong planning and task management skills �?� Proficiency with Microsoft Office applications This position is based in IPM�??s Paarl, South Africa office. Job holder should expect a fast-paced working environment. At least 30% local and international travel will be required.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Sr. Manager/Assistant Director, Investigations and Brand Protection
- Verifiable formal training w/demonstrated track record of bringing investigations to successful resolution- Working knowledge of Current Good Manufacturing Practices (cGMP) and applicable regulations set forth by the Food and Drug Administration (FDA), State Boards of Pharmacy (BOP), Department of Transportation (DOT), Department of Homeland Security (DHS) and US Customs and Border Patrol (USCBP)- Ability to travel internationally and work varied hours to accommodate time zones in countries where investigations are ongoing- Professionally recognized certification such as CPP, CFE or PCI is preferred
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Manager/Sr. Manager, Supply Chain
Minimum 7 years Supply Chain experience required. Experience within the Life Sciences field and an international supply chain background is highly preferred.Bachelor of Science or equivalent required - preferably in supply chain, operations or related discipline. MBA preferred.SAP or other ERP software experience and strong knowledge of Microsoft Office suite required.Has strong understanding of supply chain and manufacturing environments.Possesses strong cross-functional leadership capability.Succeeds at influencing a wide spectrum of stakeholders.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Director Medical Affairs, Latin America
A minimum of five (5) years in a Medical Director Role.- Medical Degree; must have a License of Medical Doctor & Board certification in at least one specialty with basic medical science and research experience. Experience focused on oncology or immunology preferred. - Strong people management skills- Basic marketing skills as well as understanding business practices and technical terms in business. - Business acumen, a bottom-line orientation, strong management and leadership skills. - Must have proficiency in both Spanish and English (Portuguese a plus) in order to interact with the other team clinicians at the corporate headquarters in the US, as well worldwide. - Present, discuss, negotiate & persuade the global team in English- Self motivated, both strategic and tactical in his/her thought process and capable of becoming rapidly engaged in the company?s business- High degree of self-direction, with the ability to quickly make decisions and accept responsibility for outcomes
Astellas Pharma, Inc.	Phoenix	AZ	9/9/2010
Sales Director PCP & Specialty- West Coast
REQUIREMENTS:- 8+ years pharmaceutical sales and sales 6 years pharmaceutical sales management experience, some of which needs to be at the director level. - Extensive knowledge of sales processes and pharmaceutical products and industry- Excellent communication, facilitation and presentation skills- Can do approach and excellent motivational and persuasion skills- Leadership skills commensurate with the position- BA/BS degree is required - Extensive travel is required for this position
Astellas Pharma, Inc.	Kalamazoo (1P040109)	MI	9/9/2010
Sr. Professional Representative I, PCP
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year) with business-to-business sales If you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Washington - East (5DC10403)	DC	9/9/2010
Sr. Executive Representative, Hospital - Washington, DC (East)
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Jacksonville (5DA20405)	FL	9/9/2010
Sr. Executive Representative, Hospital - Jacksonville, FL
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Jacksonville (1P030205)	FL	9/9/2010
Sr Professional Representative, PCP - Jacksonville (South), FL
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Extensive travel is required for this position- Some experience (1 year) with business-to-business sales If you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Yonkers (1P010208)	NY	9/9/2010
Sr Professional Representative PCP- Yonkers, NY
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year) with business-to-business sales If you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	San Jose (1P060507)	CA	9/9/2010
Sr Professional Representative PCP- Walnut Creek, CA
- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Las Vegas East (1P060208)	NV	9/9/2010
Sr Professional Representative PCP- Las Vegas East, NV
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Harrisburg (1P010609)	PA	9/9/2010
Sr Professional Representative PCP- Harrisburg, PA
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Decatur (1P030504)	GA	9/9/2010
Sr Professional Representative PCP- Decatur, GA
- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Colorado Springs (1P060106)	CO	9/9/2010
Sr Professional Representative PCP- Colorado Springs, CO
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Chico (1P060503)	CA	9/9/2010
Sr Professional Representative I PCP - Chico, CA
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year) with business-to-business sales If you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Leesburg (1P030304)	FL	9/9/2010
Sr Professional Representative PCP- Leesburg, FL
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Phoenix North (5PP50602)	AZ	9/9/2010
Sr Executive Representative Hospital- Phoenix North, AZ
REQUIREMENTS:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, Anti-Infective or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	WI (5DC40205)	Milwaukee	9/9/2010
Sr Executive Representative Hospital- Milwaukee, WI
REQUIREMENTS:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, Anti-Infective or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Seattle North (1V060202)	WA	9/9/2010
Senior Professional Representative - Specialty; Seattle North, WA
REQUIREMENTS:-3+ years pharmaceutical selling experience including 1 years promoting specialty products -Extensive knowledge of sales processes and pharmaceutical products and industry-Excellent communication, facilitation and presentation skills-Can do approach and very high motivational and persuasion skills-Proven, consistent sales record -A BA/BS degree
Astellas Pharma, Inc.	Jersey City (1V010400)	NJ	9/9/2010
Regional Sales Manager - Specialty; Jersey City, NJ
Job Requirements:- Valid driver's license - Minimum of 5-7 years experience in pharmaceutical sales or related fields, including primary care and specialty sales (preferably hospital sales experience) . - Prior experience in managing field representatives is preferred - Must provide evidence of leadership skills and successful contributions outside immediate team (i.e., training, mentoring, process development, etc.) - A demonstrated high degree of proficiency in managing multiple projects - Proven presentation, coaching, and teaching skills. - Demonstrated ability to consistently meet and exceed sales quota goals - Proficient with basic computer skills. - 4 year college degree
Astellas Pharma, Inc.	Bridgeport (1P010207)	CT	9/9/2010
Professional Representative PCP- Bridgeport, CT
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	San Francisco (5AA50505)	CA	9/9/2010
Executive Representative, Hospital- San Francisco, CA
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Harrisburg (2A020506)	PA	9/9/2010
Executive Representative, Hospital- Harrisburg, PA
REQUIREMENTS:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, Anti-Infective or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Manhattan (South)	NY	9/9/2010
Executive Representative, Hospital - Manhattan (South), NY
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is required
Astellas Pharma, Inc.	Freehold	NJ	9/9/2010
Executive Representative, Hospital - Central NJ
REQUIREMENTS:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, Anti-Infective or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Seattle North (5PP50406)	WA	9/9/2010
Executive Representative Hospital- Seattle, WA
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Vice President, Global Clinical Science
Minimally a BS Degree. Must have at least 15 years of pharmaceutical industry experience specifically in human drug development, and at least 3-5 years managing managers of multiple groups within the area of Clinical Operations/Clinical Science. Previous experience in leading a Global Clinical Operations function is preferable. Must have a successful track record in the hiring and retention of excellent clinical operations resources globally, who work optimally in a cross functional team and matrix environment. Must have a successful track record in effectively collaborating with other functions in development, discovery research, Medical Affairs and Commercial in the development and support of medicines.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Sr. Scientist/Scientist, Cell Culture Process Development - Agensys, Santa Monica, CA
? Ph.D. in a scientific discipline (Chemical Engineering, Biochemical Engineering or biology) with 5+ years of relevant experience in the pharmaceutical /biotechnology industries.? Knowledge of the design, optimization and scale-up of cell culture processes is a necessity. Direct experience with mammalian cell culture process development and process transfer for clinical or commercial manufacturing of biopharmaceutical product(s) highly preferred.? Knowledge in the use of DOE to conduct experiments? Hands-on experience with unit operations such as lab and pilot-scale bioreactor operation,centrifugation, clarification, and filtration.? Process validation and cGMP experience is desirable.? Supervisory experience preferred.? Must be highly motivated, have excellent organizational and communication skills, and must be able to work independently and as part of a multi-disciplinary team
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Sr. Director, Global Business Information Management
Minimally a BS. Must have 10- 15 years of pharmaceutical industry experience specifically in human drug development, and at least 3-5 years managing a BISM Function globally. Must have a successful track record in the hiring and retention of excellent business interface resources who work optimally in a cross functional team and matrix environment. Must have a successful track record in effectively collaborating with other functions in development, in the development and support of medicines through optimal use of relevant technologies. Must have an in-depth personal experience and understanding of the BISM function, current and future technologies needs and investment and their critical contribution to GDO's successful contribution to drug development. Must also have an understanding of the functions of multiple business units throughout the company, and have maintained effective collaborations with leadership of those business units and functions. Is considered an industry expert and is able to recognize the implications of new directions, trends and developments. Must be a strong and effective strategic thinker and problem solver, requiring the ability to both recognize and anticipate problems, and also help managers and individuals develop their own problem solving skills and discipline. However, must also be able to identify and solve tactical problems and delve into high degree of detail when necessary. Plans for and has detailed knowledge of all available resources internally and externally, has developed the appropriate relationships with partners and vendors, and has the ability to marshal those resources in a productive and efficient manner, either as part of a 3 year strategic capacity plan, or when there is need for sudden and immediate change in direction.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Senior Scientist/Group Leader, Antibody Generation and Production - Agensys, Santa Monica, CA
Ph.D. or equivalent in Immunology, Biochemistry or a related discipline, with at least 8 -10 years of demonstrated experience in a relevant field working either in an academic or bio-pharmaceutical environment. The qualified candidate will have broad experience and knowledge in all aspects of hybridoma or recombinant antibody technologies, including phage display; will be an accomplished investigator with a solid publication or patenting record. Finally the successful individual must be a self-starter, with excellent managerial, communication and interpersonal skills.
Astellas Pharma, Inc.	Skokie	IL	9/9/2010
Senior Scientist, Bioanalytical Laboratory - Pharmacodynamics
Ph.D. in molecular or cellular biology (or equivalent) with 3+ years of related industry experiences, or M.Sc. in science (major in molecular or biological sciences) with 5+ years of related industry experienceKnowledge and experience in molecular/ PCR-based testingKnowledge and experience with immunoassaysKnowledge and experience in biological sample preparationsKnowledge of FDA guideline for bioanalytical method validationWorking knowledge of SOPs and GLP regulatory guidance Ability to transfer and validate biomarkers, immunogenicity and immunoassay methods Knowledge of computer software for laboratory data management Skills in conducting bioanalytical research especially for running clinical samples, documenting data, and assisting report writing following the regulatory requirements.Self-motivated, excellent team player with good communication skills
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Senior Research Associate, Protein Mass Spectrometry- Agensys, Santa Monica, CA
Candidate consideration requires a B.S. or M.S. in chemistry, biochemistry or similar field with a minimum of 7 years of laboratory experience. Industrial or academic experience in protein and proteomic analysis by advanced mass spectrometry methods is highly preferred.Hands on experience in protein mass spectrometry method development and experience with Thermo LTQ line of instruments as well as using computational methods for MS data processing are also preferred.The successful candidate will have strong written and oral communication skills, be self-motivated, possess strong organizational skills, and have a track record of working successfully in a team environment.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Senior Research Associate / Research Associate ? Molecular Biology - Agensys, Santa Monica, CA
Position requires a BS or MS in Molecular Biology or a related field with a minimum 2 years of practical application in a research laboratory. Experience in RNA analysis, and database management are preferable. Excellent verbal and communication skills, and the ability to work in a team environment are required.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Senior Project Manager, DDPM
Bachelors Degree required. Advanced degree (masters, doctorate) a plus. Generally, seven (7) years with Masters Degree or ten plus (10+) years relevant experience with a minimum five to seven (5-7) years experience with a demonstrated understanding of the drug development process, and project management skills required. Knowledge of required CMC, pharmacology, toxicology, PK, clinical requirements to support major US regulatory filings ? IND, NDA, etc.Demonstrates clear depth and breadth of understanding of critical early drug development processes Demonstrated expertise /discipline in project management and a key organizer who has shown to set clear priorities on developmental activities, with experience in planning systems (e.g. MSProject) and an understanding of financial planning / expenditures. Good communication, people management and social skills with a good sense of diplomacy both in a scientific and industrial environment.Effectively utilizes information technology systems and provisional project management tools.Capable of managing meetings within a multicultural environment and organize expert meetings with KOLs.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Senior Medical Writing Program Manager, Oncology
BA/BS degree or equivalent; 10+ years relevant experience. Preferred: MS/MA/MPH with at least 7 years as a writing professional in pharmaceutical industry.Activities require expert technical skill (e.g., as defined by Drug Information Association Medical Writing Competency Model) including techniques of scientific writing and editing; ability to interpret and communicate clinical and numerical data, and verify consistency in data; comprehend and communicate scientific concepts; interpret and communicate clinical, nonclinical, biopharmaceutic, pharmacology, ADME and CMC data and information.Activities require advanced document and process experience, and highly complex problem solving/issue resolution to achieve corporate objective(s), resourcefulness and sharing of expertise.Technical expert for the majority of document types produced by medical writing. Demonstrated and substantial experience in managing the creation of IND/IMPD or NDA/MAA components, briefing documents and white papers.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Scientist/Senior Scientist, Antibody Drug Conjugates, Drug Discovery - Agensys, Santa Monica, CA
PhD in biological sciences, with 5+ years of relevant industrial experiencePrevious background with chemotherapeutic drugs, monoclonal antibodies and/or antibody drug conjugates for oncology with some in vivo tumor biology experience is highly preferred.Excellent analytical, oral and written communication skills and a demonstrated ability to operate both independently and in a team environment.Strong data analytical skills, excellent communication and supervisory skills are required.The qualified candidate should be a highly motivated, strategic thinker with excellent organizational skills who can effectively drive programs forward in a cross functional team oriented environment.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Scientist, Process Development in Antibody Drug Conjugates - Agensys, Santa Monica, CA
? Ph.D. in a scientific discipline (Chemistry, Chemical Engineering, and Biology) with 5+ years of relevant experience in the pharmaceutical /biotechnology industries.? Knowledge of the design, optimization and scale-up of organic synthesis processes. ? Direct experience in protein purification, conjugation of monoclonal antibodies to small molecules, and process scale-up. ? Experience with HPLC, LC/MS-ESI, chromatographic techniques and immunologic assays including ELISA and immunoblotting? Hands-on experience with unit operations such as lab and pilot-scale bioreactor operation, chromatography, UF/DF, and filtration? Supervisory experience and experience with coordinating activities with CMOs are preferred.? Must be highly motivated, have excellent organizational and communication skills, and must be able to work independently and as part of a multi-disciplinary team.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Safety Scientist/Principal Safety Scientist, Oncology
Minimum of Bachelor?s Degree in Science or Pharmacy or Nursing required.Minimum of 5 years pharmaceutical experience in a clinical safety/research department required.Minimum of 5 years of medical writing experience (Prefer experience in writing pharmaceutical reports such as Clinical Study Reports, Safety sections of the ISS and/or EU Common Technical document, PSUR or white paper).Proven ability to critically evaluate medical data.Proven understanding of clinical disease state and implications of treatment.Proven ability to communicate effectively (verbal, presentation at group meetings, etc).Proven experience with project management (formal or informal).Prefer experience in training or mentoring.Strategic thinking, Organizational, Leadership, Results-oriented performance, Team player.Excellent knowledge of ICH, US & EU regulations and requirements for pharmacovigilance (experience with world-wide safety reporting regulations and guidelines required).Excellent interpersonal skills, including ability to work effectively cross culturally and cross functionally.Proven ability to effectively lead cross-functional teams with respect to risk management activities and to influence where direct reporting line relationships do not exist. Excellent written and spoken English
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Research Scientist, Pharmacology - Agensys - Santa Monica, CA
Candidate consideration requires a Ph.D., or an equivalent degree, in Biology, Pharmacology, Immunology, Biochemistry or a related field with a minimum of 3 years of post-doctoral experience. Previous hand-on experience using human tumor xenograft models in oncology research, as evidenced by publications, is required. Understanding the basic concepts of pharmacokinetics and pharmacodynamics and be able to analyze relevant data are highly desired. Experience in human tumor xenograft and primary cell line development is a definite plus. Previous experience in preclinical evaluation of cancer therapeutics using xenograft models preferably in an industry drug discovery setting and experience managing research associates are preferred. Successful candidates should have strong written and oral communication skills, be self-motivated and able to demonstrate leadership. Developmental opportunities include leading research projects and building new technology platforms.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Research Quality Assurance Associate - Agensys, Santa Monica, CA
? PhD in Life Sciences preferred.? Minimum 2 years in a pharmaceutical development environment with solid knowledge and review experience of in-vivo and in-vitro study protocols and reports. Additional quality assurance experience in a research environment with programs such as document management and equipment qualification is recommended.? In-depth understanding of pre-clinical pharmacology studies. ? Strong oral and written communication skills are required.? Strong interpersonal skills and the ability to work in a project team environment are a requirement. ? Fluency with Word, Excel, and Access databases is recommended.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Research Associate/Senior Research Associate: Target function ? MAb assays - Agensys, Santa Monica, CA
The position requires a BS or MS in Biology or a related field with a minimum 3 years of practical experience in a research laboratory in the required activities. Industry experience and previous work in biochemical, immunological, cell culture and cell-based techniques are essential. Excellent verbal and communication skills, and the ability to work both independently and in a team environment are required.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Research Associate/Senior Research Associate: Antibody Drug Discovery - Agensys, Santa Monica, CA
The position requires a BS or MS in Biology or a related field with a minimum 3 years of practical experience in a research laboratory in the required activities. Previous work in biochemical, immunological, cell culture and cell-based techniques are essential. Industrial experience is preferred. Excellent verbal and communication skills and the ability to work both independently and in a team environment are required.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Research Associate/ Senior Research Associate ? Molecular Biology - Agensys, Santa Monica, CA
The ideal candidate will have M.S. (preferred) or B.S. in Molecular Biology or related field, with a minimum of five (5) years of relevant research experience. Experience in molecular biology techniques and methods, with emphasis on gene expression and gene structure analysis is required. The ability to reliably handle and process precious and limited specimens is essential. Excellent verbal and written communication skills, as well as the ability to work both independently and in a team environment are required.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Research Associate, Protein Science - Agensys, Santa Monica, CA
Candidate consideration requires a B.S. or M.S. in chemistry, biochemistry or similar field with a minimum of 2 years of laboratory experience. Industrial experience protein analysis and protein purification is highly preferred. Experience in proteomic method development and hands on experience with Biacore are also preferred. The successful candidate will have strong written and oral communication skills, be self-motivated, possess strong organizational skills, and have a track record of working successfully in a team environment.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Research Associate /Senior Research Associate in vivo validation, Agensys - Santa Monica, CA
The ideal candidate should have a bachelor or master degree in biological sciences with a minimum of 2 years of related research experience after graduation, preferably in an industry setting. Previous experiences in handling research rodents, especially immunodeficient mice in oncology research and human cancer cell culture are absolutely required. Experiences in pre-clinical validation of cancer therapeutics using human tumor xenograft models, microsurgical procedures in laboratory rodents, human tumor xenograft characterization and human cancer primary cell line establishment are highly desired. We are seeking a flexible, enthusiastic individual with good organizational and communication skills and the desire to work in a dynamic team environment.
Astellas Pharma, Inc.	Skokie	IL	9/9/2010
Research & Development Future Opportunities
? Positions in the Research & Development division at Astellas require degrees in science; advanced degrees plus industry experience are preferred.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Quality Control Microbiologist - Agensys, Santa Monica, CA
? A Bachelor?s degree or equivalent work experience in microbiology or science discipline. Must have 1 ? 2 years experience in a GMP Microbiology pharmaceutical or biopharmaceutical environment. Familiarity with cGMP manufacturing a plus.? Must have strong teamwork and organizational skills ? Resourceful, self-reliant, self-motivated, and confident ? Excellent verbal and written communication skills ? The ability to multitask and exercise good judgment ? Detailed oriented with good follow-up skills ? Assist with administrative tasks related to the department ? Maintains good aseptic technique, housekeeping, order, and safety in the laboratory? Maintain logbooks, record and report all test results in a timely manner ? Revise procedures as necessary to improve efficiency and ensure compliance with regulatory requirements ? Must be familiar with Microsoft Word and Excel
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
QA Associate I - Agensys, Santa Monica, CA
? Minimum 3-5 years GMP experience required? BA or BS Degree in Life Sciences or 5-7 years of professional GMP experience? Previous Quality Assurance signature approval of controlled documents required? Strong computer skills recommended, experience with Access / Trackwise highly desirable? Strong oral and written communication skills required? Experience reviewing, creating, and implementing Standard Operating Procedures preferred? Experience with equipment validations preferred
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Project Manager/Senior Project Manager, DDPM
Bachelors Degree required. Advanced degree (masters, doctorate) a plus. Generally, five (5) years with Masters Degree or seven plus (7+) years relevant experience with a minimum of three to five (3-5) years experience directly related to drug development process with a demonstrated understanding of the drug development process, and project management skills required. Knowledge of required CMC, pharmacology, toxicology, PK, clinical requirements to support major US regulatory filings ? IND, NDA, etc.Demonstrated expertise /discipline in project management and a key organizer who has shown to set clear priorities on developmental activities, with experience in planning systems (e.g. MSProject) and an understanding of financial planning / expenditures. Good communication, people management and social skills with a good sense of diplomacy both in a scientific and industrial environment.Effectively utilizes information technology systems and provisional project management tools.Capable of managing meetings within a multicultural environment and organize expert meetings with KOLs.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Project Management Specialist - Agensys, Santa Monica, CA
The ideal candidate will have a university degree and a minimum of 5 ? 8 years related experience in Project Management or in Drug Development ? preferably both. Even more preferable would be Drug development project management experience in biologics or biologic-based drugs. Working knowledge of PM tools such as MS Project and MS Excel is required. Experience in initiating and implementing additional communication, planning, scheduling and development strategy software tools are a plus. Excellent communication skills and the ability to work in a team environment are essential. PMP certification a plus but not essential
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Principal Safety Scientist
Minimum of Bachelor?s Degree in Science or Pharmacy or Nursing required.Minimum of 5 years pharmaceutical experience in a clinical safety/research department required.Minimum of 5 years of medical writing experience (Prefer experience in writing pharmaceutical reports such as Clinical Study Reports, Safety sections of the ISS and/or EU Common Technical document, PSUR or white paper).Proven ability to critically evaluate medical data.Proven understanding of clinical disease state and implications of treatment.Proven ability to communicate effectively (verbal, presentation at group meetings, etc).Proven experience with project management (formal or informal).Prefer experience in training or mentoring.Strategic thinking, Organizational, Leadership, Results-oriented performance, Team player.Excellent knowledge of ICH, US & EU regulations and requirements for pharmacovigilance (experience with world-wide safety reporting regulations and guidelines Excellent interpersonal skills, including ability to work effectively cross culturally and cross functionally.Proven ability to effectively lead cross-functional teams with respect to risk management activities and to influence where direct reporting line relationships do not exist. Excellent written and spoken English
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
PET Senior Research Associate- Agensys, Santa Monica, CA
This position requires a Bachelor/Master?s Degree of Science and at least three years of direct animal research experience utilizing microPET/CT systems; an associates degree and Five years animal research experience with at least 3 years utilizing PET/CT; or eight years directly related animal research experience with 5 years utilizing PET/CT .AALAS certification at the LATG level is also required. The qualified individual must possess excellent organizational and communication skills, exhibit problem solving skills, as well as a desire to learn new techniques and train others in a team environment. This role also requires the individual to be "results-driven" with the ability to think through processes in order to improve efficiency and outcome of studies required.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Medical/Senior Medical Director, Pharmacovigilance- Oncology
SUPERVISORY RESPONSIBILITY: Directly supervises Assistant Medical Director(s), Associate Medical Director(s), and/or Medical Director(s) in the PSP Department.KNOWLEDGE & EXPERIENCE: Identify specialized knowledge needed to perform the position. The years of experience are not required. Note if the specific knowledge or skill is required, desirable, or a plus.MD degree, Pharmaceutical Industry experience in Pharmacovigilance and drug safety for at least five years, Team working, analytical skills, and flexibility are essential for this position.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Medical Director/Senior Medical Director, Oncology
M.D. degree or equivalent; Board Certified or Board Eligible in oncology highly desirableMinimum 6 or more years experience in the pharmaceutical industry or equivalent academic experience.Strong working-knowledge of regulatory procedures and guidelines (preferably global)Experience in P1-3 clinical development; prior EU/US regulatory filing experience expected.Holds others accountableStrong industry acumen, vision and perspective
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Medical Director, Product Safety & Pharmacovigilance
This position is responsible for strategies in pre and post marketing risk management, as well as keeping abreast of pharmacovigilance methods and trends in published literature and global regulations. Additionally responsible for strategies in monitoring and analysis of cumulative safety information on Astellas products. Responsible for drug safety crisis managementSpecific responsibilities include:Guides regulatory reporting including individual case safety reports (ICSRs), NDA annual report summary statements, and Periodic Safety Update Reports (PSURs)Guides adverse event coding, retrieval and analysis activities in drug safety and clinical trialsGuides reviews of safety sections of NDA submissionsPlans cumulative safety information analysis such as signal detection from company or public databases with data miningGuides safety updates of company core data sheet and local product labelsGuides pharmacoepidemiology projectsGuides crisis management on drug safetyGuides Risk Management Plans for specific productsGuides and coordinates preparation of ad-hoc benefit-risk assessment documentsGuides regulatory strategy and preparation of data related safety to regulatory authorities and advisory committeesInterfaces with Medical Sciences, Clinical Studies, Product Safety Management, Drug Development and Project Management, Pharmacoepidemiology, Global Pharmacovigilance departments, Toxicologist, Biopharmaceutical sciences, Research Data Sciences, Legal Demonstrated leadership skills and strategic focus. Demonstrated ability to exercise independent judgment and effectively collaborate with multiple functional unitsPosition requirements: MD degree, Pharmaceutical Industry experience in Pharmacovigilance and drug safety for at least five years, Team working, analytical skills, and flexibility are essential for this position
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Medical Director, Medical Sciences- Oncology
M.D. degree, Board Certified or Board Eligible in Oncology/Hematology.Minimum three years clinical experienceMinimum two years laboratory or clinical research experience and five years experience in the pharmaceutical industry or equivalent academic experience.Knowledge of regulatory procedures and guidelines (preferably global)Experience in clinical development, preferably experience in at least 2 phases Effective team player in a matrixed R&D environmentAble to work independently on all aspects of assigned projectsExcellent presentation and writing skillsExcellent organizational skills
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Manager/Senior Manager CMC Analytical Development - Agensys, Santa Monica, CA
PhD in chemistry, biochemistry or biology with 10+ years experience in development, qualification, and transfer of chromatographic, spectrophotometric, electrophoretic, and other relevant analytical methods for protein biotherapeutics in a biopharmaceutical environment. -hands-on experience and a good understanding of LC-MS and MS/MS for biologics is a must; the ability to troubleshoot complex technical and scientific problems; an in-depth understanding of protein characterization techniques: proven supervisory and managerial skills are essential; -a high level of expertise with cGMP, and regulatory compliance in biotechnology product development is expected; -experience with immunological methods is a strong plus; experience with analytical test method development for small molecular is preferable. Must be able to perform in a fast paced multiproduct environment.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Laboratory Manager - Agensys, Santa Monica, CA
EDUCATION: B.S./M.S. degree in Science.Experience: At least five years of Lab management experienceThe successful candidate must demonstrate a strong working knowledge of pharmaceutical/biotechnology research laboratories and their unique safety issues, including vivarium facilities and familiarity with IACUC regulations. Experience in industry is strongly preferred. Strong written and verbal communication skills, as well as interpersonal skills are also essential. In addition, the successful candidate must have the ability to demonstrate leadership and problem solving skills in a team based environment.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Global Development Project Leader - Central Nervous System
An MD, PhD or PharmD is preferable with a specialty in the CNS therapeutic area required along with experience in global development. Experience in the area of Alzheimer disease preferred. Total leadership experience including line/project management. multidisciplinary program management experience, which includes leadership in more than one IND/IMPD, NDA/MAA, Advisory Committee or other PMDA/EMEA/FDA meetings.Minimum of ten (10) years experience in drug development in pharmaceuticals, biopharmaceuticals, or biotechnology.Demonstrated experience leading the development of at least one development candidate with adherence to quality, excellence and efficiency.Demonstrated experience leading drug development projects and activities in a matrixed, global organization. A broad understanding of how to communicate and work well with team members and relevant people as well as scientists and external decision-makers worldwide. A thorough understanding of how to influence local and global regulatory, scientific and commercial environments.Skill Set:o Ability to assimilate data, recognize key variables and analyze complex situations. Make quality judgments.o Has a realistic expectation of the business, one?s self and others.o A style which builds alliances within the organization, locally/globally, and/or corporate collaborators.o Does not confuse effort for results.o Tenacity to weather short-term setbacks for long-term advantages.o Broad understanding of the multidisciplinary functions contributing to effective and efficient drug development.Solid understanding of CMC, pharmacology, toxicology, PK, clinical requirements to support major regulatory filings ? IND/IMPD, NDA/MAA.Leads preparation of PMDA/EMEA/FDA milestone meetings, such as Pre-IND, End-of-Phase II, Pre-NDA, Advisory Committees, focusing on the key strategic issues.Excellent understanding of the interdependencies of the various disciplines (CMC, Pharm/Tox, PK, Clinical, Regulatory, Marketing, Finance, etc) - what needs to be evaluated simultaneously vs. sequentially etc. from a strategic planning/risk management time/event/cost point locally and globally.Understanding of how to educate/advise others on Regulatory Guidances/Internal SOPs/PM concepts.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Director/Senior Director, Global Development Project Lead, Oncology
An MD, PhD or PharmD is preferable with a specialty in the assigned oncology area, or equivalent experience with global development required. Total leadership experience including line/project management. multidisciplinary program management experience, which includes leadership in more than one IND/IMPD, NDA/MAA, Advisory Committee or other PMDA/EMEA/FDA meetings.Minimum of ten (10) years experience in drug development in pharmaceuticals, biopharmaceuticals, or biotechnology.Demonstrated experience leading the development of at least one development candidate with adherence to quality, excellence and efficiency.Demonstrated experience leading drug development projects and activities in a matrixed, global organization. A broad understanding of how to communicate and work well with team members and relevant people as well as scientists and external decision-makers worldwide. A thorough understanding of how to influence local and global regulatory, scientific and commercial environments.Skill Set:o Ability to assimilate data, recognize key variables and analyze complex situations. Make quality judgments.o Has a realistic expectation of the business, one?s self and others.o A style which builds alliances within the organization, locally/globally, and/or corporate collaborators.o Does not confuse effort for results.o Tenacity to weather short-term setbacks for long-term advantages.o Broad understanding of the multidisciplinary functions contributing to effective and efficient drug development.Solid understanding of CMC, pharmacology, toxicology, PK, clinical requirements to support major regulatory filings ? IND/IMPD, NDA/MAA.Leads preparation of PMDA/EMEA/FDA milestone meetings, such as Pre-IND, End-of-Phase II, Pre-NDA, Advisory Committees, focusing on the key strategic issues.Excellent understanding of the interdependencies of the various disciplines (CMC, Pharm/Tox, PK, Clinical, Regulatory, Marketing, Finance, etc) - what needs to be evaluated simultaneously vs. sequentially etc. from a strategic planning/risk management time/event/cost point locally and globally.Understanding of how to educate/advise others on Regulatory Guidances/Internal SOPs/PM concepts.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Director, Translational Research - Agensys, Santa Monica, CA
Candidate consideration requires a Ph.D./M.D. with a minimum of 10 years of post-doctoral experience. Industrial experience in Oncology drug discovery and experience managing scientists is required. Successful candidates will have strong written and oral communication skills, be self-motivated, demonstrate leadership and possess an exemplary record of research, as evidenced by publications and patents.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Director, in vivo Pharmacology - Agensys, Santa Monica, CA
Candidate consideration requires a Ph.D. with a minimum of 10 years of post-doctoral experience. Industrial experience in Oncology drug discovery and experience managing scientists is required. Successful candidates will have strong written and oral communication skills, be self-motivated, demonstrate leadership and possess an exemplary record of research, as evidenced by publications and patents
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Cell Culture Associate - Agensys, Santa Monica, CA
? A B.S. or M.S. in biochemistry, biology, biochemical engineering or a related field. ? >3 years related experience in the biopharmaceutical/biotech industrial ? Prior hands-on experiences in cell culture process development, especially with shake flasks and bioreactors.? Operation experience with pilot-scale bioreactors will be plus ? Possess good problem solving, organizational, and documentation skills with a strong focus on details? Must have excellent organizational and communication skills? Must be highly motivated, be able to work independently as well as in teams
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Asst. Animal Technician/Animal Technician/Sr. Animal Technician - Agensys, Santa Monica, CA
Previous husbandry experience of laboratory rodents is highly desirableAn ALAT or higher certification and understanding of AAALAC accreditation are a plus. A BA/BS degree is a definite plusThe successful candidate must follow all animal health standards, stringent SOP?s and safety protocols, be able to lift objects of approximately 50 pounds and should have no allergies to common laboratory rodentsThe incumbent should have a general appreciation for biological science and an understanding of the intricacies of laboratory research.This person should have good verbal and written communication skills and the ability to work well in a team environment with a positive/can-do attitude.The person should also be detail-oriented and willing to work flexible hours.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Associate/Sr. Associate, Cell Line Development, Agensys, Santa Monica, CA
? The ideal candidates will have a B.S. or M.S. in Biology, Molecular Biology, Biochemical Engineering,or related field, with preferably a minimum of 2 years of relevant experience in industry.? Experience in generation of transient/stable cell lines and mammalian cell culture are required.? Working knowledge of antibody expression and detection in mammalian cells is preferred.? Compliance with appropriate written procedures; e.g. applicable safety, biological containment, and administrative procedures is required. ? Excellent written and oral communication skills and the ability to work in a team environment are essential.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Associate Manager, Outsourcing
Bachelors Degree in Business, Life Sciences or equivalent experience, Master?s Degree or other Advanced degree preferred.Generally 7 + years experience required in R&D Outsourcing, Clinical or Business Operations within a pharmaceutical company required.Strong analytical and problem solving skills and ability to come up with creative solutions.Strong team player.Demonstrated negotiation and influencing skills.Demonstrated ability to provide leadership.Demonstrated ability to strategically manage vendor relationships.Demonstrated ability to manage multiple projects simultaneously.Demonstrated ability to effectively communicate across all levels of management. Advanced use of word processing and spreadsheet software. Strong written and oral communications skills
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Associate Director, Quality Assurance - Agensys, Santa Monica, CA
1. Minimum BA / BS or equivalent, advanced degree preferred, with a minimum of 10 years of industry experience, 6 years of QA experience, and 3 - 5 years managing staff. 2. Comprehensive knowledge of GxP and other regulations and understanding of global quality standards relating to product development, submission and/or commercialization. Ability to contribute to local and global Quality policies in support of the quality system. 3. Effective written and oral communication and interpersonal skills, facilitation, and influencing skills with an demonstrated ability to lead projects, initiatives, or programs across multiple departments, regions and business units within Astellas group and external stakeholders. Demonstrated ability to solicit input and liaise with stakeholders to prioritize and set strategic direction for change. 4. Demonstrated ability to assess the state of current business and QA operations for Quality Systems to identify and recommend future state, improvements, and to implement action plans. 5. Demonstrated competence to resolve complex and diverse problems with decision making responsibility that has a major impact (e.g., stakeholder relationships, dossier approvals, compliance status, credibility and/or revenue) within QA and within the region. 6. Demonstrated experience developing quality strategies and priorities and translating them into short and long-term objectives for the department. Ability to provide leadership to Quality Systems programs, initiatives and teams, with minimal management oversight. 7. Demonstrated ability to develop quality assurance professionals and to both lead and manage a functional quality assurance unit.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Associate Director, CPED Science, Oncology
Minimum MS or equivalent qualification in a bio-medical/science field required. MD or PhD desired.The Assistant/Associate Director role requires at least 5-7 years post-graduate experience, in pharmaceutical industry, preferably from another (major) Pharma Company with a general understanding of Drug Discovery and Development. In addition, the individual should have the following experiences.Expert knowledge of disease biology and relevant clinical disease knowledge required to design early development strategies up to and including PoC.Expert knowledge of Clinical Pharmacology Knowledge and proven development expertise in at least 3 therapeutic areas.Team player with strong written and communication skills to bring over and get acceptance for plans.Strong, critical analytical mindOperate with minimum of supervision.Key organizer and planner who clearly sets priorities.Up to date with latest ICH-GCP guidelines and other relevant regulations.Highly developed sense for ethical conduct of Clinical Development
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Associate Director, Clinical Pharmacology - Agensys, Santa Monica, CA
? PhD, PharmD, MS, BS in Pharmacy or life sciences with extensive training in pharmacology, pharmacokinetics, and pharmacodynamics and data analysis -- also beneficial to have experience with population PK/PD modeling and simulation? 8-10 years of Phase I clinical trial experience or equivalent? 5 years of experience with oncology drug development? 5 years of experience with antibodies ? Knowledge of global drug development process and ability to design and implement development plans? Extensive experience in representing Clinical Pharmacology to regulatory agencies ? Established leadership skills? Proven communication, management and leadership skills
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Associate Director / Director Statistics
MS or PhD in statistics or mathematics; minimum of 7-10 years in pharma or CRO industry, with minimum of 2-4 years in functional or project management roleAt least 2 years experience in working on global clinical studies and projects or global process and system initiativesVery good understanding of all phases of clinical development, and processes in data scienceExperience in all aspects of statistics for clinical trials, and in working as a member of a project team including design of clinical studies and contribution to Clinical Development PlansExperience as lead statistician for multiple submissions to health authorities, substantial experience in interations with health authoritiesGood understanding of the various functions and expert groups contributing to Drug Development Solid knowledge of SAS and other statistical toolsMinimum requirements for Director level:Generally a minimum of 10 years of relevant experience in pharma or CRO industryMinimum of 4-5 years of management experience including 2-3 years in a line management positionDemonstrated ability to translate strategic plan for GDO, Data Science and Statistics into goals and objectives for own functionDemonstrated leadership skills and ability to effectively prioritize own group?s activities for development projects and clinical trialsProven ability to establish operating guidelines and procedures, preferably in a global settingDemonstrated ability to successfully identify and lead global process or system improvement initiatives
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Associate Biostatistics Director, Oncology
M.S. or Ph.D. in statistics or equivalentRequired proven oncology experience Minimum of 8 years experience in applying statistical methods in biomedical research, extensive pharmaceutical or CRO experience requiredExperience in working on clinical project teams. Good understanding of entire drug development process - ability to see the ?big picture?.Experience as the independent lead statistician in a regulatory submission preferredExperience with cross functional process improvement or innovation initiativesAdvanced and broad knowledge of statistical methods, along with understanding of industry practices related to the statistical analysis of clinical dataKnowledge and skills in SAS required and knowledge of other statistical software preferred.In-depth familiarity with processes and procedures in data management and SAS programmingExperience working in an international environment and demonstrated ability to manage and influence across different locations, time zones and cultures; builds global relationships. Ability to work in a matrix environment. Proven excellent organizational, project and time management skills.Leadership skills and ability to delegate appropriately and provide direction to more junior Biostatisticians. Very good oral, written, and presentation communication skills. Able to clearly communicate statistical issues and methods to both statisticians and non-statisticians. Very good problem solving skills.Accurate with a keen eye for detail. Dedication to quality and reliability in all work tasksAbility to perform under pressure
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Analytical Associate/Sr. Analytical Associate, Process Development - Agensys, Santa Monica, CA
The successful candidate will possess the following qualifications.? B.S. or M.S. in biochemistry, chemistry, or related field with at least three-year experience inbiotechnology/biopharmaceutical industry.? Experience in protein analysis by HPLC, gel electrophoresis, UV/Vis spectroscopy, and plate-basedprotein assays such as BCA and ELISA. Experience in CE and DSC is a plus
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
: Senior Scientist/Scientist, Applied Molecular Biology - Agensys, Santa Monica, CA
The successful candidate will have a PhD in molecular biology, biotechnology, biochemistry or related discipline with minimum 7 years of relevant industry experience. Other required experience includes expertise in a broad range of molecular and cellular techniques surrounding aspects of microarray-based discovery for biomarker and pathway identification, and knowledge of computational analysis of large data sets. Industrial experience in oncology drug discovery is preferred. Successful candidate will have excellent verbal and communication skills, demonstrate leadership and ability to work in a dynamic team environment.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Director / Senior Director, Discovery - Agensys, Santa Monica, CA
? Advanced degree (Ph.D., or equivalent) with at least 10 years? experience in an industry setting in Drug Discovery and related areas with an emphasis on target discovery and validation, and monoclonal antibody discovery and engineering. ? Strong background in Oncology drug discovery, evidenced by involvement in development of product candidates from initiation to clinical stage, some experience with biologics is preferred.? Demonstrated record in driving scientific and technical innovations, as evidenced by first or senior authored publications in top-tiered journals.? Demonstrated successful program leadership and multi-project coordination. ? At least 5 years of management experience of multiple groups. ? Proven track record in leading programs to achieve goals and timelines.? Ability to perform successfully in a cross-functional team environment.? Excellent written and verbal communication skills.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Associate Director, Regulatory Affairs
KNOWLEDGE & EXPERIENCE: ? Bachelor?s degree in scientific discipline; advanced degree preferred.? 9 years previous pharmaceutical drug development experience, 2 in managing staff.? Recognized as an expert in regulatory aspects of pharmaceutical drug development involving undefined frameworks with technical complexity and broad scope.? Scientific knowledge in chemistry, general biological/physical science and ability to apply that knowledge to regulatory issues and product development. Recognized as an expert in an aspect of pharmaceutical drug development. ? 6 years regulatory affairs experience preferably involving direct contact with the FDA; full knowledge of FDA and ICH regulations and guidelines, and the ability to provide interpretations of that information to others. Proven record of successful IND/NDA submissions and negotiations with the FDA in areas of CMC and product formulations. Regulatory experience in other therapeutic areas such as medical devices or biologics.? Strong organizational skills with the ability to manage large projects and provide regulatory guidance/training to direct reports and others in the department as needed.? Proven ability to prioritize and multi-task with minimal supervision based on interactions with project team members.? Ability to communicate effectively and maintain effective working relationships. Must be able to positively influence department staff and other APGD groups.? High integrity with respect to maintenance of proprietary, confidential information. ? Excellent written and oral communication skills, with writing ability to meet regulatory requirements and standards.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Director, Quality Systems
Minimum BA / BS or equivalent, advanced degree preferred, with a minimum of 10+ years of industry experience, 8 years of QA experience, and 4 ? 6 years managing staff.Experience in managing a Quality System within a GCP / Pharmacovigilance environment. Comprehensive knowledge of GxP and other regulations and understanding of global quality standards relating to product development, submission and/or commercialization. Establishes local and regional Quality policies in support of the quality system.Effective written and oral communication and interpersonal skills. Influencing skills with a demonstrated ability to lead projects, initiatives, or programs across multiple departments, regions and business units within Astellas group and external stakeholders. Demonstrated ability to solicit input and liaise with stakeholders to prioritize and set strategic direction for change.Demonstrated ability to assess the state of current business and QA operations for Quality Systems to identify and recommend future state, improvements, and to implement action plans.Demonstrated competence to resolve complex and diverse problems with decision making responsibility that has a major impact within QA and/or with functional groups within the region.Demonstrated experience leading strategic development and successful execution of plans and initiatives for addressing complex and diverse QA matters with minimal management oversight. Contributes to the identification and implementation of long-term business planning strategies, assuring quality is taken into consideration. Demonstrated ability to develop quality assurance professionals to both lead and manage a functional quality assurance unit.Demonstrated experience in hosting and facilitating regulatory agency inspections with successful outcomes.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Director Quality Assurance - Agensys, Santa Monica, CA
1. Minimum BA/BS degree with 8 years experience in Quality and 4 years managing staff and 10+ years in the pharmaceutical industry. 2. Comprehensive knowledge of GCP , GLP, and GMP and other regulations relating to product development, testing, submission and commercialization.3. Ability to contribute ideas for strategies and tactics to ensure adequate long term planning for the quality assurance function.4. Ability to establish standards in support of the quality system and to interface across multiple departments and levels of management.5. Practical experience of line management position while demonstrating a desire for creative, hands-on approach to leadership in support of a fast growing organization.6. Effective project management skills and commitment to meeting deadlines and work well under pressure.7. Excellent written and oral communication, facilitation and influencing skills with an ability to work within an environment which utilizes both in-house and out-sourced (contract/temporary) resources.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Associate Director, Quality Assurance, R&D Programs, GCP
Minimum BA / BS or equivalent, science-related preferred, with 10 years of industry experience, 6 years of QA experience, and 3-5 years managing staff.GCP Quality Assurance experience required and experience in a pharmaceutical manufacturing or clinical development environment preferred. Comprehensive knowledge of GCP regulations and understanding of global quality standards relating to product development, submission and/or commercialization. Demonstrated ability to establish local and regional Quality policies and to contribute to global Quality policies in support of the quality system.Ability to assist or lead strategic development and/or successful execution of plans and initiatives that ensure long term success for R&D Programs GCP at a Regional or Global level with minimal management oversight. Demonstrated accountability to resolve complex and diverse problems with decision making responsibility that has a significant impact (e.g., stakeholder relationships, dossier approvals, compliance status, credibility and/or revenue) within QA and across the APGD.Demonstrated ability to anticipate, proactively respond to trends, and/or shifts in the external environment (e.g., regulatory, business partner relationships, industry standards) and to predict impact on quality assurance and/or Astellas business units.Effective written and oral communication and interpersonal skills, facilitation, and influencing skills with an ability to interface regionally across multiple departments, and among various levels of management within Astellas group and external stakeholders. Demonstrated ability to solicit input and liaise with stakeholders to prioritize and set strategic direction for change. Assist in the identification and implementation of short and long-term business planning strategies, assuring quality is taken into consideration.Demonstrated ability to develop quality assurance professionals and to both lead and manage a functional quality assurance unit.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Assistant Director, Quality Systems
Minimum BA / BS or equivalent, advanced degree preferred, with a minimum 10 years of industry experience, 6 years of QA experience, and 3-5 years managing staff.Comprehensive knowledge of GxP and other regulations and understanding of global quality standards relating to product development, and commercialization. Ability to contribute to local and global Quality policies in support of the quality system.Effective written and oral communication and interpersonal skills, facilitation, and influencing skills with an demonstrated ability to lead projects, initiatives, or programs across multiple departments, regions and business units within Astellas group and external stakeholders. Demonstrated ability to solicit input and liaise with stakeholders to prioritize and set direction for change.Demonstrated ability to assess the state of current business and QA operations for Quality Systems to identify and recommend future state, improvements, and to implement action plans.Demonstrated competence to resolve complex and diverse problems with decision making responsibility that has a major impact (e.g., stakeholder relationships, dossier approvals, compliance status, credibility and/or revenue) within QA and within the region.Demonstrated experience developing quality strategies and priorities and translating them into short and long-term objectives for the department. Ability to provide leadership to Commercial Products and GMP programs, initiatives and teams, with minimal management oversight. Demonstrated ability to develop quality assurance professionals and to both lead and manage a functional quality assurance unit.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Assistant Director Marketing Analytics - IL, Deerfield
?X Bachelor��s degree is required, Master��s degree preferred, preferably in business or the sciences.?X Must have a minimum of 7-10 years successful experience in the pharmaceutical or other related healthcare field in the area of market research and analysis.?X Extensive computer proficiency with desktop software in a Windows environment required: Microsoft Word; Microsoft Excel; Power Point required, Microsoft Access; Cognos; Spotfire; and other Statistical software a plus.?X Excellent skills in the following areas: organization, written and verbal communication, accuracy and personal initiative.?X Must have a minimum of 1-3 years supervisory experience.?X Experience in forecasting, market model development is a strong positive.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Associate Marketing Director, Latin America
? 7-10 years of experience? Infectious Disease/Oncology experience.? English/Spanish required. Portuguese desirable.Required Qualifications:1. Bachelor's degree in a related discipline with an advanced degree in business. Science degree preferred. Marketing experience in specific therapeutic area may be required.2. 10+ years of relevant experience depending on degree, including 5 years marketing leadership experience within the Pharmaceutical industry.3. Global and regional marketing experience required preferably in Latin America.4. Requires significant communication and leadership skills and the ability to create and implement the Marketing Plan and integrate it with APLA objectives.5. Strong relationship management and influencing skills and comfort working with cross-functional teams.6. Excellent oral and written communication skills. Ability to understand and help define business questions and present findings in a compelling manner to various audiences.7. Ability to travel domestically and internationally required (up to 50%).8. Fluent in Spanish/English with Portuguese highly desirable.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Manufacturing Associate II, Bioprocess -- Agensys, Santa Monica, CA
BS in biological or other science related field and 3+ years relevant industrial experience in the manufacture or development of FDA regulated Biological Products. Clinical or commercial manufacturing experience preferred. Broad based technical knowledge with manufacturing equipment (i.e. Bioreactors, filtration, mixers, purification etc.). Excellent organizational skills, written and oral communication skills and ability to multi-task. Must possess mechanical aptitude.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Manufacturing Associate II, Bioprocess - Agensys, Santa Monica, CA
BS in biological or other science related field and 3+ years relevant industrial experience in the manufacture or development of FDA regulated Biological Products. Clinical or commercial manufacturing experience preferred. Broad based technical knowledge with manufacturing equipment (i.e. Bioreactors, filtration, mixers, purification etc.). Excellent organizational skills, written and oral communication skills and ability to multi-task. Must possess mechanical aptitude.
Astellas Pharma, Inc.	Oklahoma City	OK	9/9/2010
Manager, Engineering
? BS in chemical or mechanical engineering or equivalent relevant pharmaceutical science field required. Advanced degree preferred.? A minimum of 5 ? 8 years experience in solid dosage pharmaceutical manufacturing including packaging required.? A minimum two years management of engineers experience required.. ? Additional knowledge in at least one of the following areas is beneficial: Statistical Inference, SPC, Process Capability, DOE, Sampling plan or Risk Assessment.? Must be able to read, write and understand the English language (statement common to all Job Descriptions) ? Must be able to work to meet deadlines, and utilize problem solving skills. Must be able to gather and evaluate complex data to make effective decisions to accomplish work. Strong communication, prioritization and organizational skills. Attention to detail required. Ability to work independently and as a team member. Accurate record keeping.? Minimum supervision required
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Facilities Department Planner/Assistant- Agensys, Santa Monica, CA
? An Associates of Arts degree? A minimum of two years experience working in a pharmaceutical FDA regulated environment? A working knowledge of Computerized Maintenance Management Systems? Self-starter with the ability to work with minimum supervision? Excellent verbal and written communication skills? The ability to multitask and exercise good judgment? The ability to work in a fast pace environment and maintain a high level of customer service? Detailed oriented with good follow-up skills? Proficient in computer usage with standard business software
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Sr. Manager, Network & Security
10+ years broad Information Technology experienceProven leadership skills and a passion for operations excellenceRequires an in-depth understanding of networking and security technology including routers, routing protocols, firewalls, switches, intrusion detection and prevention systems, DLP, VPN, wireless and endpoint protectionExcellent project management, analytical and organizational skillsStrong problem solving and troubleshooting skillsStrong written, verbal and presentation skillsCCIE, CISSP, and ITIL certifications are a plusBachelor?s degree or equivalent
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Sr. Manager, Information Management
10+ years broad Information Technology experience5+ years direct IT experience in:Data & Information Architecture developmentConceptual and strategic IT planning and developmentData Warehouse Project ManagementIBM Infosphere and Cognos suite of productsSAP BW and Business Objects product suite Other significant experience in:Building and managing high performance teamsDeveloping strong partnerships with internal business groupsBuilding IT practicesData modelingDatabase toolsReporting toolsExcellent verbal and written communication skillsExcellent problem solving and analytical abilityIT degree or equivalent experienceProven track record of exceptional success
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Sr. Analyst, IT Quality
Bachelor?s Degree in Computer Science, related field, or equivalent experience required.5 + years relevant experience related to change management, document development, and application testing.Working knowledge of computer systems validation processes, system development life cycle, and Change Management processes. Must exhibit creativity and innovation in solutions; be broadly focused and able to manage multiple efforts concurrently.Exceptional attention to details and ability to consistently produce high quality and accurate work.Has solid interpersonal and communications skills (written, oral, and non-verbal) to effectively relate to technical staff and business customers.Ability to be self-directed within the scope of their duties and responsibilities.Ability to build and maintain positive and cooperative working relationships by demonstrating collaborative behaviors and cross functional facilitation skills.Understand the pharmaceutical industry and IT best practices.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Senior Director, IT Client Relationship Management
Serves as the IT liaison for a specific enterprise wide business unitManages the IT resources dedicated to the business unit or functionWorks directly with the senior leadership of the business unit and IT Performs or directs high level activities with appropriate awareness of other activities within the organizationServes as a business advocate to IT and an IT advocate to the businessResolves complex business issues that affect cross functional areas or multiple sitesDirects the IT application and support requirements from a staffing perspectiveKeeps the Business and IT informed of important changes in each of the respective areas Leads complex business process reengineering projects Controls project priorities and ensures balance between business needs and IT resource constraintsResponsible for project delivery, providing ongoing updates and advocacy to the Business and IT Meets regularly with business personnel to define, review or revise:IT support strategiesApplication portfolioProject priorities and statusSystems supportApplications and infrastructure service levelsApplication growth projections and new access requirementsDirects the development and documentation of IT Strategies and Plans as a member of the IT Senior Management TeamWorking jointly with key business contact(s), manages the IT budgets, projects and prioritiesExtensive knowledge and skill through broad and/or deep experiences in Pharma IT Strong communication and interpersonal skills, capable of motivating and influencing teamsPerform at the highest levels and able to make decisions on their ownAble to translate between technical and business leaders at the highest levelsViewed as credible, and well respected by the business and IT organizationsAccountability in building and maintaining positive and cooperative working relationships Fifteen or more years of relevant experience within the pharmaceutical industry Collaboration and cross functional facilitation skillsHigh level understanding of project management, quality assurance, and IT best practicesProficiency with commercial applications that are designed to support enterprise wide business capabilitiesAdvanced Degree required (or progress towards and significant industry experience)
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Associate Director, Global Strategy IT Projects
Bachelors Degree required. Advanced degree (masters, doctorate) a plus. Generally, ten plus (10+) years relevant IT experience or equivalent proven project management experience in an IT capacity within the pharmaceutical, biopharmaceutical, or biotechnology industries. Global experience preferred.Proven history of successful program management experienceA key organizer who has shown to set clear priorities on developmental activities and finances with experience in financial reporting and planning systems. A demonstrated leader in a matrix organization, able to motivate and inspire local team members to high performance levels.Good communication, people management and social skills with a good sense of diplomacy both in an IT and other environments.Excellent understanding of the interdependencies of the various disciplines (e.g. R&D, Legal, HR, Supply Chain, Marketing, and Finance). This will include an understanding of what needs to be evaluated simultaneously vs. sequentially from both a local and a global project management perspective.Understanding of how to educate/advise others on IT/Internal SOPs/PM concepts
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Associate Director, Human Resources
Bachelor?s degree in Human Resources or Business, or equivalent experience required. Master?s degree preferred.Seven to ten years related experience required, preferably in the pharmaceutical or healthcare industries. Three to five years management experience required.Demonstrated Human Resources generalist knowledge required, specifically including employment law.Incumbent must have demonstrated ability to work in a challenging, multi-cultural work environment.Ability to manage confidential information imperative, including influencing others to maintain the confidentiality of sensitive information.Some travel required, up to 50% depending on assigned organizations.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Associate Director, Compensation
Minimum of 10+ years of experience in human resources with at least seven years compensation experience. Experience in the pharmaceutical industry preferred. Requires Bachelors Degree, MBA preferred.Excellent knowledge of HR/compensation practices and principles, and all applicable labor, pay, benefits, health and safety laws and regulations. Excellent, planning, time management, communication, decision-making, presentation, organization, and interpersonal skills.Strategic business partner, good communicator with excellent interpersonal skills. Ability to communicate and present information to all levels within and outside the organization in a comprehensible manner. A team player with outstanding leadership skills. Detail oriented and accurate. Proactive. Solid mathematical aptitude and analysis skills. Knowledge of human resources automated systems. Work requires professional written and verbal communication and interpersonal skills. Ability to motivate teams to produce quality materials within tight timeframes and simultaneously manage several projects.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Senior Maintenance Mechanic - Agensys, Santa Monica, CA
? A High School Diploma? Ten years relevant experience in Bio-Pharmaceutical, petrochemical, packaging or power generation industries with at least four years of that in a pharmaceutical FDA regulated GMP environment ? Demonstrated abilities and /or evidence of training in the repair, operations and troubleshooting of electromechanical process equipment, HVAC systems and utility systems? The ability to read blueprints and P&ID?s? Good communication skills verbal and written? Good computer and keyboard skills, proficient with standard business software
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Sr. Manager, Clinical Studies, Oncology
University/College degree with seven years clinical trials experience is desired. Proven time and project management skills, knowledge of drug development process and proven leadership ability is required. Working knowledge of ICH and GCP guidelines is required. Experience in people management is preferred.Proven track record in oncology required. Must have excellent interpersonal, written and verbal communication skills, administrative skills and computer ability. Travel required.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Senior Manager/Associate Director, Clinical Study Management Support
Minimum requirements of Senior Manager level:BA/BS degree with at least 7 years of clinical trial management and/or clinical document management experience; advance degree preferred (MS/PhD) with at least 5 years clinical trial and/or clinical document management experience.Minimum of 2 years of people management experience.Must have expertise in implementing operational strategies and strong knowledge of ICH/GCP guidelines and regulatory requirements.Must have detailed understanding of the clinical research and drug development process and experience handling associated documents.Must have strong computer skills and knowledge of information and document management systems.Must have proven and effective interpersonal, leadership, written and verbal communication skills.Fluent in English; minimal (<10%) travel required.Minimum requirements for Associate Director level:BA/BS degree with at least 10 years of clinical trial management and/or clinical document management experience; advanced degree preferred (MS/PhD) with at least 7 years clinical trial and/or clinical document management experience.Minimum of 4 years of people management experience.Must have extensive experience in implementing operational strategies and strong knowledge of ICH/GCP guidelines and regulatory requirements.Demonstrated ability to translate strategic plan for GDO and Clinical Site and Document Management into goals and objectives for function.Demonstrated leadership skills and ability to effectively prioritize own group?s activities for development projects and clinical trials.Proven ability to establish operating guidelines and procedures, preferably in a global setting.Demonstrated ability to successfully identify and lead global process or system improvement initiatives.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Senior Manager, Clinical Studies
University/College degree with seven years clinical trials experience is desired. Proven time and project management skills, knowledge of drug development process and proven leadership ability is required. Working knowledge of ICH and GCP guidelines is required. Experience in people management is preferred. Must have excellent interpersonal, written and verbal communication skills, administrative skills and computer ability. Travel required.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Senior Director, Statistics & Clinical Programming
Minimally a PhD in Statistics, or equivalent Degree, with specialization in Pharmaceutical Drug Development or equivalent work experience. Must have at least 10-15 years of pharmaceutical industry experience specifically in human drug development, and at least 3-5 years managing managers within a biometrics, biostatics function in clinical development. Preferably, will have successfully led a global Biostatistics and Programming function in a major pharmaceutical company. Must have a successful track record in the hiring and retention of excellent statistical and data management scientists who work optimally in a cross functional team and matrix environment. Must have a successful track record in effectively collaborating with other functions in development, discovery research, Medical Affairs and Commercial in the development and support of medicines. Must have an in-depth personal experience and understanding of the relevant expert groups within the Statistics and Programming function and their critical contribution to drug development. Must also have an understanding of the functions of multiple business units throughout the company, and have maintained effective collaborations with leadership of those business units and functions. Is considered an industry expert and is able to recognize the implications of new directions, trends and developments in the area of design, acquisition and reporting of data in the pharmaceutical industry. Must have extensive knowledge of the application of statistical analysis and reporting tools. Must be a strong and effective strategic thinker and problem solver, requiring the ability to both recognize and anticipate problems, and also help managers and individuals develop their own problem solving skills and discipline. However, must also be able to identify and solve tactical problems and delve into high degree of detail when necessary. Plans for and has detailed knowledge of all available resources internally and externally, has developed the appropriate relationships with partners and vendors, and has the ability to marshal those resources in a productive and efficient manner, either as part of a 3 year strategic capacity plan, or when there is need for sudden and immediate change in direction.Displays the highest level of personal commitment to the Astellas code of Ethics. Is exemplary in ensuring that "every employee deserves a great manager". Inspires while holds all appropriately accountable. Commits through co-accountability, to the growth and health of GDO, APGD and Astellas.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Senior Director, Global PK Modeling & Simulation
PhD in Life Sciences required. Must have at least 10 or more years of pharmaceutical industry experience, specifically in global human drug development, both in exploratory development, late clinical pharmacology and later phases of development. Broad therapeutic area knowledge and prior experience with biologicals is important. Extensive knowledge experience in application of PKMS in global drug development, both in Exploratory Development as wel as late CP. Good understanding of Late Development as well as Drug Discovery.Good knowledge of mathematics and power of mathematical modelsMust have a successful track record in interactions with Global Regulatory authorities; prior experience contributing to successful regulatory filings highly important. Must have a successful track record in the hiring and retention of excellent scientists who work optimally in a cross functional team and matrix environment. Must have a successful track record in effectively collaborating with other functions in development, discovery research, Medical Affairs and Commercial in the development and support of medicines. Displays the highest level of personal commitment to the Astellas code of Ethics. Is exemplary in ensuring that "every employee deserves a great manager". Inspires while holds all appropriately accountable. Commits through co-accountability, to the growth and health of GCPED, APGD and Astellas.Must have an in-depth personal experience and understanding of the GCPED function and its critical contribution to drug development. Must have extensive experience in interactions with global Regulatory Authorities. Must also have an understanding of the functions of multiple business units throughout the company, and have maintained effective collaborations with leadership of those business units and functions. Is considered an industry expert and is able to recognize the implications of new directions, trends and developments as it relates to GCPED and Astellas business. Must be a strong and effective strategic thinker and problem solver, requiring the ability to both recognize and anticipate problems, and also help managers and individuals develop their own problem solving skills and discipline. However, must also be able to identify and solve tactical problems and delve into high degree of detail when necessary. Plans for and has detailed knowledge of all available resources internally and externally, has developed the appropriate relationships with partners and vendors, and has the ability to marshal those resources in a productive and efficient manner, either as part of a 1-3 year strategic capacity plan, or when there is need for sudden and immediate change in direction.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Senior Director, Clinical Study Management
Minimally a BS. Must have at least 10 years of pharmaceutical industry experience specifically in human drug development, and at least 3-5 years managing managers of Clinical Study Managers in multiple therapeutic and geographic areas. Must have a successful track record in the hiring and retention of excellent clinical operations resources globally, who work optimally in a cross functional team and matrix environment. Must have a successful track record in effectively collaborating with other development functions in the development and support of medicines. Must have an in-depth personal experience and understanding of the Clinical Science function and the critical contribution of Clinical Operations to drug development, Must also have an understanding of the functions of multiple business units throughout the company, and have maintained effective collaborations with leadership of those business units and functions. Is considered an industry expert and is able to recognize the implications of new directions, trends and developments globally and on a multi-country and regional level, in site and patient recruitment, site monitoring, essential document collection and management, and the optimal use of cross functional outsourcing relationships. Must be a strong and effective strategic thinker and problem solver, requiring the ability to both recognize and anticipate problems, and also help managers and individuals develop their own problem solving skills and discipline. However, must also be able to identify and solve tactical problems and delve into high degree of detail when necessary. Plans for and has detailed knowledge of all available resources internally and externally, has developed the appropriate relationships with partners and vendors, and has the ability to marshal those resources in a productive and efficient manner, either as part of a 3 year strategic capacity plan, or when there is need for sudden and immediate change in direction.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Clinical Research Specialist
University/College Degree or previous healthcare experience desired. Must have excellent interpersonal, written and verbal communication skills, administrative skills and computer abilities. Minimum travel required.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Associate Director, Clinical Studies
B.S./B.A. life sciences degree or B.S.N or R.N. and ten years clinical research experience with four years experience in the management of people; M.S. degree and seven years related clinical research experience with four years people management experience; Pharm. D. or Ph.D. degree and five years of clinical research experience and a minimum of four years managing people. Must have excellent interpersonal skills, written and verbal communication skills, administrative skills and computer ability as well as in depth knowledge of the clinical drug development process and clinical study design and planning. He/she must be able to rapidly grasp medical concepts in a variety of therapeutic areas. Experience in project management and strategic planning is preferred. Ideal candidate will have managed a project leading to a New Drug Application or Product License Application. Candidate must also have proven management and leadership ability, knowledge of FDA/GCP requirements and familiarity with the pharmaceutical industry. Moderate (20-40%) travel required.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Associate Director / Director, Clinical Study Management
BA/BS degree with at least 10 years clinical trial management experience; advanced degree (MS, PhD, PharmD) preferred with 7 years clinical trial management experienceMinimum of 4 years people management experienceMust have extensive expertise in developing operational strategies and strong knowledge of ICH/ GCP guidelines and multinational clinical trial regulations.Must have extensive experience in people and project management, strategic planning and a strong knowledge of protocol and clinical drug development processes, clinical study design, study planning and management.Must have experience working across multiple molecules, indications and phases of development. Must have proven and effective interpersonal, leadership, written and verbal communication skills, administrative skills and computer ability. Fluent in English; low to moderate (5% to 20%) travel required.Minimum requirements for Director level:BA/BS degree with at least 12 years of clinical trial management experience; advance degree preferred (MS/PhD/PharmD) with at least 8 years clinical trial management experienceMinimum of 6 years of people management experienceDemonstrated ability to translate strategic plan for GDO and Clinical Science into goals and objectives for functionDemonstrated leadership skills and ability to effectively prioritize own group?s activities for development projects and clinical trialsProven ability to establish operating guidelines and procedures, preferably in a global settingDemonstrated ability to successfully identify and lead global process or system improvement initiatives
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Financial Analyst - Agensys, Santa Monica, CA
? B.S, degree in a Accounting or business preferred.? 3 to 6 years of financial data analysis experience.? Excellent skill in manipulating Excel spreadsheets.? Ability to develop meaningful reports from complex data sources.? Strong knowledge of GAAP.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Sr. Manager/Assistant Director, Investigations and Brand Protection
- Verifiable formal training w/demonstrated track record of bringing investigations to successful resolution- Working knowledge of Current Good Manufacturing Practices (cGMP) and applicable regulations set forth by the Food and Drug Administration (FDA), State Boards of Pharmacy (BOP), Department of Transportation (DOT), Department of Homeland Security (DHS) and US Customs and Border Patrol (USCBP)- Ability to travel internationally and work varied hours to accommodate time zones in countries where investigations are ongoing- Professionally recognized certification such as CPP, CFE or PCI is preferred
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Manager/Sr. Manager, Supply Chain
Minimum 7 years Supply Chain experience required. Experience within the Life Sciences field and an international supply chain background is highly preferred.Bachelor of Science or equivalent required - preferably in supply chain, operations or related discipline. MBA preferred.SAP or other ERP software experience and strong knowledge of Microsoft Office suite required.Has strong understanding of supply chain and manufacturing environments.Possesses strong cross-functional leadership capability.Succeeds at influencing a wide spectrum of stakeholders.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Director Medical Affairs, Latin America
A minimum of five (5) years in a Medical Director Role.- Medical Degree; must have a License of Medical Doctor & Board certification in at least one specialty with basic medical science and research experience. Experience focused on oncology or immunology preferred. - Strong people management skills- Basic marketing skills as well as understanding business practices and technical terms in business. - Business acumen, a bottom-line orientation, strong management and leadership skills. - Must have proficiency in both Spanish and English (Portuguese a plus) in order to interact with the other team clinicians at the corporate headquarters in the US, as well worldwide. - Present, discuss, negotiate & persuade the global team in English- Self motivated, both strategic and tactical in his/her thought process and capable of becoming rapidly engaged in the company?s business- High degree of self-direction, with the ability to quickly make decisions and accept responsibility for outcomes
Astellas Pharma, Inc.	Phoenix	AZ	9/9/2010
Sales Director PCP & Specialty- West Coast
REQUIREMENTS:- 8+ years pharmaceutical sales and sales 6 years pharmaceutical sales management experience, some of which needs to be at the director level. - Extensive knowledge of sales processes and pharmaceutical products and industry- Excellent communication, facilitation and presentation skills- Can do approach and excellent motivational and persuasion skills- Leadership skills commensurate with the position- BA/BS degree is required - Extensive travel is required for this position
Astellas Pharma, Inc.	Kalamazoo (1P040109)	MI	9/9/2010
Sr. Professional Representative I, PCP
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year) with business-to-business sales If you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Washington - East (5DC10403)	DC	9/9/2010
Sr. Executive Representative, Hospital - Washington, DC (East)
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Jacksonville (5DA20405)	FL	9/9/2010
Sr. Executive Representative, Hospital - Jacksonville, FL
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Jacksonville (1P030205)	FL	9/9/2010
Sr Professional Representative, PCP - Jacksonville (South), FL
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Extensive travel is required for this position- Some experience (1 year) with business-to-business sales If you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Yonkers (1P010208)	NY	9/9/2010
Sr Professional Representative PCP- Yonkers, NY
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year) with business-to-business sales If you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	San Jose (1P060507)	CA	9/9/2010
Sr Professional Representative PCP- Walnut Creek, CA
- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Las Vegas East (1P060208)	NV	9/9/2010
Sr Professional Representative PCP- Las Vegas East, NV
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Harrisburg (1P010609)	PA	9/9/2010
Sr Professional Representative PCP- Harrisburg, PA
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Decatur (1P030504)	GA	9/9/2010
Sr Professional Representative PCP- Decatur, GA
- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Colorado Springs (1P060106)	CO	9/9/2010
Sr Professional Representative PCP- Colorado Springs, CO
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Chico (1P060503)	CA	9/9/2010
Sr Professional Representative I PCP - Chico, CA
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year) with business-to-business sales If you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Leesburg (1P030304)	FL	9/9/2010
Sr Professional Representative PCP- Leesburg, FL
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Phoenix North (5PP50602)	AZ	9/9/2010
Sr Executive Representative Hospital- Phoenix North, AZ
REQUIREMENTS:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, Anti-Infective or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	WI (5DC40205)	Milwaukee	9/9/2010
Sr Executive Representative Hospital- Milwaukee, WI
REQUIREMENTS:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, Anti-Infective or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Seattle North (1V060202)	WA	9/9/2010
Senior Professional Representative - Specialty; Seattle North, WA
REQUIREMENTS:-3+ years pharmaceutical selling experience including 1 years promoting specialty products -Extensive knowledge of sales processes and pharmaceutical products and industry-Excellent communication, facilitation and presentation skills-Can do approach and very high motivational and persuasion skills-Proven, consistent sales record -A BA/BS degree
Astellas Pharma, Inc.	Jersey City (1V010400)	NJ	9/9/2010
Regional Sales Manager - Specialty; Jersey City, NJ
Job Requirements:- Valid driver's license - Minimum of 5-7 years experience in pharmaceutical sales or related fields, including primary care and specialty sales (preferably hospital sales experience) . - Prior experience in managing field representatives is preferred - Must provide evidence of leadership skills and successful contributions outside immediate team (i.e., training, mentoring, process development, etc.) - A demonstrated high degree of proficiency in managing multiple projects - Proven presentation, coaching, and teaching skills. - Demonstrated ability to consistently meet and exceed sales quota goals - Proficient with basic computer skills. - 4 year college degree
Astellas Pharma, Inc.	Bridgeport (1P010207)	CT	9/9/2010
Professional Representative PCP- Bridgeport, CT
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	San Francisco (5AA50505)	CA	9/9/2010
Executive Representative, Hospital- San Francisco, CA
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Harrisburg (2A020506)	PA	9/9/2010
Executive Representative, Hospital- Harrisburg, PA
REQUIREMENTS:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, Anti-Infective or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Manhattan (South)	NY	9/9/2010
Executive Representative, Hospital - Manhattan (South), NY
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is required
Astellas Pharma, Inc.	Freehold	NJ	9/9/2010
Executive Representative, Hospital - Central NJ
REQUIREMENTS:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, Anti-Infective or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Seattle North (5PP50406)	WA	9/9/2010
Executive Representative Hospital- Seattle, WA
THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Vice President, Global Clinical Science
Minimally a BS Degree. Must have at least 15 years of pharmaceutical industry experience specifically in human drug development, and at least 3-5 years managing managers of multiple groups within the area of Clinical Operations/Clinical Science. Previous experience in leading a Global Clinical Operations function is preferable. Must have a successful track record in the hiring and retention of excellent clinical operations resources globally, who work optimally in a cross functional team and matrix environment. Must have a successful track record in effectively collaborating with other functions in development, discovery research, Medical Affairs and Commercial in the development and support of medicines.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Sr. Scientist/Scientist, Cell Culture Process Development - Agensys, Santa Monica, CA
? Ph.D. in a scientific discipline (Chemical Engineering, Biochemical Engineering or biology) with 5+ years of relevant experience in the pharmaceutical /biotechnology industries.? Knowledge of the design, optimization and scale-up of cell culture processes is a necessity. Direct experience with mammalian cell culture process development and process transfer for clinical or commercial manufacturing of biopharmaceutical product(s) highly preferred.? Knowledge in the use of DOE to conduct experiments? Hands-on experience with unit operations such as lab and pilot-scale bioreactor operation,centrifugation, clarification, and filtration.? Process validation and cGMP experience is desirable.? Supervisory experience preferred.? Must be highly motivated, have excellent organizational and communication skills, and must be able to work independently and as part of a multi-disciplinary team
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Sr. Director, Global Business Information Management
Minimally a BS. Must have 10- 15 years of pharmaceutical industry experience specifically in human drug development, and at least 3-5 years managing a BISM Function globally. Must have a successful track record in the hiring and retention of excellent business interface resources who work optimally in a cross functional team and matrix environment. Must have a successful track record in effectively collaborating with other functions in development, in the development and support of medicines through optimal use of relevant technologies. Must have an in-depth personal experience and understanding of the BISM function, current and future technologies needs and investment and their critical contribution to GDO's successful contribution to drug development. Must also have an understanding of the functions of multiple business units throughout the company, and have maintained effective collaborations with leadership of those business units and functions. Is considered an industry expert and is able to recognize the implications of new directions, trends and developments. Must be a strong and effective strategic thinker and problem solver, requiring the ability to both recognize and anticipate problems, and also help managers and individuals develop their own problem solving skills and discipline. However, must also be able to identify and solve tactical problems and delve into high degree of detail when necessary. Plans for and has detailed knowledge of all available resources internally and externally, has developed the appropriate relationships with partners and vendors, and has the ability to marshal those resources in a productive and efficient manner, either as part of a 3 year strategic capacity plan, or when there is need for sudden and immediate change in direction.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Senior Scientist/Group Leader, Antibody Generation and Production - Agensys, Santa Monica, CA
Ph.D. or equivalent in Immunology, Biochemistry or a related discipline, with at least 8 -10 years of demonstrated experience in a relevant field working either in an academic or bio-pharmaceutical environment. The qualified candidate will have broad experience and knowledge in all aspects of hybridoma or recombinant antibody technologies, including phage display; will be an accomplished investigator with a solid publication or patenting record. Finally the successful individual must be a self-starter, with excellent managerial, communication and interpersonal skills.
Astellas Pharma, Inc.	Skokie	IL	9/9/2010
Senior Scientist, Bioanalytical Laboratory - Pharmacodynamics
Ph.D. in molecular or cellular biology (or equivalent) with 3+ years of related industry experiences, or M.Sc. in science (major in molecular or biological sciences) with 5+ years of related industry experienceKnowledge and experience in molecular/ PCR-based testingKnowledge and experience with immunoassaysKnowledge and experience in biological sample preparationsKnowledge of FDA guideline for bioanalytical method validationWorking knowledge of SOPs and GLP regulatory guidance Ability to transfer and validate biomarkers, immunogenicity and immunoassay methods Knowledge of computer software for laboratory data management Skills in conducting bioanalytical research especially for running clinical samples, documenting data, and assisting report writing following the regulatory requirements.Self-motivated, excellent team player with good communication skills
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Senior Research Associate, Protein Mass Spectrometry- Agensys, Santa Monica, CA
Candidate consideration requires a B.S. or M.S. in chemistry, biochemistry or similar field with a minimum of 7 years of laboratory experience. Industrial or academic experience in protein and proteomic analysis by advanced mass spectrometry methods is highly preferred.Hands on experience in protein mass spectrometry method development and experience with Thermo LTQ line of instruments as well as using computational methods for MS data processing are also preferred.The successful candidate will have strong written and oral communication skills, be self-motivated, possess strong organizational skills, and have a track record of working successfully in a team environment.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Senior Research Associate / Research Associate ? Molecular Biology - Agensys, Santa Monica, CA
Position requires a BS or MS in Molecular Biology or a related field with a minimum 2 years of practical application in a research laboratory. Experience in RNA analysis, and database management are preferable. Excellent verbal and communication skills, and the ability to work in a team environment are required.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Senior Project Manager, DDPM
Bachelors Degree required. Advanced degree (masters, doctorate) a plus. Generally, seven (7) years with Masters Degree or ten plus (10+) years relevant experience with a minimum five to seven (5-7) years experience with a demonstrated understanding of the drug development process, and project management skills required. Knowledge of required CMC, pharmacology, toxicology, PK, clinical requirements to support major US regulatory filings ? IND, NDA, etc.Demonstrates clear depth and breadth of understanding of critical early drug development processes Demonstrated expertise /discipline in project management and a key organizer who has shown to set clear priorities on developmental activities, with experience in planning systems (e.g. MSProject) and an understanding of financial planning / expenditures. Good communication, people management and social skills with a good sense of diplomacy both in a scientific and industrial environment.Effectively utilizes information technology systems and provisional project management tools.Capable of managing meetings within a multicultural environment and organize expert meetings with KOLs.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Senior Medical Writing Program Manager, Oncology
BA/BS degree or equivalent; 10+ years relevant experience. Preferred: MS/MA/MPH with at least 7 years as a writing professional in pharmaceutical industry.Activities require expert technical skill (e.g., as defined by Drug Information Association Medical Writing Competency Model) including techniques of scientific writing and editing; ability to interpret and communicate clinical and numerical data, and verify consistency in data; comprehend and communicate scientific concepts; interpret and communicate clinical, nonclinical, biopharmaceutic, pharmacology, ADME and CMC data and information.Activities require advanced document and process experience, and highly complex problem solving/issue resolution to achieve corporate objective(s), resourcefulness and sharing of expertise.Technical expert for the majority of document types produced by medical writing. Demonstrated and substantial experience in managing the creation of IND/IMPD or NDA/MAA components, briefing documents and white papers.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Scientist/Senior Scientist, Antibody Drug Conjugates, Drug Discovery - Agensys, Santa Monica, CA
PhD in biological sciences, with 5+ years of relevant industrial experiencePrevious background with chemotherapeutic drugs, monoclonal antibodies and/or antibody drug conjugates for oncology with some in vivo tumor biology experience is highly preferred.Excellent analytical, oral and written communication skills and a demonstrated ability to operate both independently and in a team environment.Strong data analytical skills, excellent communication and supervisory skills are required.The qualified candidate should be a highly motivated, strategic thinker with excellent organizational skills who can effectively drive programs forward in a cross functional team oriented environment.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Scientist, Process Development in Antibody Drug Conjugates - Agensys, Santa Monica, CA
? Ph.D. in a scientific discipline (Chemistry, Chemical Engineering, and Biology) with 5+ years of relevant experience in the pharmaceutical /biotechnology industries.? Knowledge of the design, optimization and scale-up of organic synthesis processes. ? Direct experience in protein purification, conjugation of monoclonal antibodies to small molecules, and process scale-up. ? Experience with HPLC, LC/MS-ESI, chromatographic techniques and immunologic assays including ELISA and immunoblotting? Hands-on experience with unit operations such as lab and pilot-scale bioreactor operation, chromatography, UF/DF, and filtration? Supervisory experience and experience with coordinating activities with CMOs are preferred.? Must be highly motivated, have excellent organizational and communication skills, and must be able to work independently and as part of a multi-disciplinary team.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Safety Scientist/Principal Safety Scientist, Oncology
Minimum of Bachelor?s Degree in Science or Pharmacy or Nursing required.Minimum of 5 years pharmaceutical experience in a clinical safety/research department required.Minimum of 5 years of medical writing experience (Prefer experience in writing pharmaceutical reports such as Clinical Study Reports, Safety sections of the ISS and/or EU Common Technical document, PSUR or white paper).Proven ability to critically evaluate medical data.Proven understanding of clinical disease state and implications of treatment.Proven ability to communicate effectively (verbal, presentation at group meetings, etc).Proven experience with project management (formal or informal).Prefer experience in training or mentoring.Strategic thinking, Organizational, Leadership, Results-oriented performance, Team player.Excellent knowledge of ICH, US & EU regulations and requirements for pharmacovigilance (experience with world-wide safety reporting regulations and guidelines required).Excellent interpersonal skills, including ability to work effectively cross culturally and cross functionally.Proven ability to effectively lead cross-functional teams with respect to risk management activities and to influence where direct reporting line relationships do not exist. Excellent written and spoken English
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Research Scientist, Pharmacology - Agensys - Santa Monica, CA
Candidate consideration requires a Ph.D., or an equivalent degree, in Biology, Pharmacology, Immunology, Biochemistry or a related field with a minimum of 3 years of post-doctoral experience. Previous hand-on experience using human tumor xenograft models in oncology research, as evidenced by publications, is required. Understanding the basic concepts of pharmacokinetics and pharmacodynamics and be able to analyze relevant data are highly desired. Experience in human tumor xenograft and primary cell line development is a definite plus. Previous experience in preclinical evaluation of cancer therapeutics using xenograft models preferably in an industry drug discovery setting and experience managing research associates are preferred. Successful candidates should have strong written and oral communication skills, be self-motivated and able to demonstrate leadership. Developmental opportunities include leading research projects and building new technology platforms.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Research Quality Assurance Associate - Agensys, Santa Monica, CA
? PhD in Life Sciences preferred.? Minimum 2 years in a pharmaceutical development environment with solid knowledge and review experience of in-vivo and in-vitro study protocols and reports. Additional quality assurance experience in a research environment with programs such as document management and equipment qualification is recommended.? In-depth understanding of pre-clinical pharmacology studies. ? Strong oral and written communication skills are required.? Strong interpersonal skills and the ability to work in a project team environment are a requirement. ? Fluency with Word, Excel, and Access databases is recommended.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Research Associate/Senior Research Associate: Target function ? MAb assays - Agensys, Santa Monica, CA
The position requires a BS or MS in Biology or a related field with a minimum 3 years of practical experience in a research laboratory in the required activities. Industry experience and previous work in biochemical, immunological, cell culture and cell-based techniques are essential. Excellent verbal and communication skills, and the ability to work both independently and in a team environment are required.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Research Associate/Senior Research Associate: Antibody Drug Discovery - Agensys, Santa Monica, CA
The position requires a BS or MS in Biology or a related field with a minimum 3 years of practical experience in a research laboratory in the required activities. Previous work in biochemical, immunological, cell culture and cell-based techniques are essential. Industrial experience is preferred. Excellent verbal and communication skills and the ability to work both independently and in a team environment are required.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Research Associate/ Senior Research Associate ? Molecular Biology - Agensys, Santa Monica, CA
The ideal candidate will have M.S. (preferred) or B.S. in Molecular Biology or related field, with a minimum of five (5) years of relevant research experience. Experience in molecular biology techniques and methods, with emphasis on gene expression and gene structure analysis is required. The ability to reliably handle and process precious and limited specimens is essential. Excellent verbal and written communication skills, as well as the ability to work both independently and in a team environment are required.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Research Associate, Protein Science - Agensys, Santa Monica, CA
Candidate consideration requires a B.S. or M.S. in chemistry, biochemistry or similar field with a minimum of 2 years of laboratory experience. Industrial experience protein analysis and protein purification is highly preferred. Experience in proteomic method development and hands on experience with Biacore are also preferred. The successful candidate will have strong written and oral communication skills, be self-motivated, possess strong organizational skills, and have a track record of working successfully in a team environment.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Research Associate /Senior Research Associate in vivo validation, Agensys - Santa Monica, CA
The ideal candidate should have a bachelor or master degree in biological sciences with a minimum of 2 years of related research experience after graduation, preferably in an industry setting. Previous experiences in handling research rodents, especially immunodeficient mice in oncology research and human cancer cell culture are absolutely required. Experiences in pre-clinical validation of cancer therapeutics using human tumor xenograft models, microsurgical procedures in laboratory rodents, human tumor xenograft characterization and human cancer primary cell line establishment are highly desired. We are seeking a flexible, enthusiastic individual with good organizational and communication skills and the desire to work in a dynamic team environment.
Astellas Pharma, Inc.	Skokie	IL	9/9/2010
Research & Development Future Opportunities
? Positions in the Research & Development division at Astellas require degrees in science; advanced degrees plus industry experience are preferred.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Quality Control Microbiologist - Agensys, Santa Monica, CA
? A Bachelor?s degree or equivalent work experience in microbiology or science discipline. Must have 1 ? 2 years experience in a GMP Microbiology pharmaceutical or biopharmaceutical environment. Familiarity with cGMP manufacturing a plus.? Must have strong teamwork and organizational skills ? Resourceful, self-reliant, self-motivated, and confident ? Excellent verbal and written communication skills ? The ability to multitask and exercise good judgment ? Detailed oriented with good follow-up skills ? Assist with administrative tasks related to the department ? Maintains good aseptic technique, housekeeping, order, and safety in the laboratory? Maintain logbooks, record and report all test results in a timely manner ? Revise procedures as necessary to improve efficiency and ensure compliance with regulatory requirements ? Must be familiar with Microsoft Word and Excel
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
QA Associate I - Agensys, Santa Monica, CA
? Minimum 3-5 years GMP experience required? BA or BS Degree in Life Sciences or 5-7 years of professional GMP experience? Previous Quality Assurance signature approval of controlled documents required? Strong computer skills recommended, experience with Access / Trackwise highly desirable? Strong oral and written communication skills required? Experience reviewing, creating, and implementing Standard Operating Procedures preferred? Experience with equipment validations preferred
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Project Manager/Senior Project Manager, DDPM
Bachelors Degree required. Advanced degree (masters, doctorate) a plus. Generally, five (5) years with Masters Degree or seven plus (7+) years relevant experience with a minimum of three to five (3-5) years experience directly related to drug development process with a demonstrated understanding of the drug development process, and project management skills required. Knowledge of required CMC, pharmacology, toxicology, PK, clinical requirements to support major US regulatory filings ? IND, NDA, etc.Demonstrated expertise /discipline in project management and a key organizer who has shown to set clear priorities on developmental activities, with experience in planning systems (e.g. MSProject) and an understanding of financial planning / expenditures. Good communication, people management and social skills with a good sense of diplomacy both in a scientific and industrial environment.Effectively utilizes information technology systems and provisional project management tools.Capable of managing meetings within a multicultural environment and organize expert meetings with KOLs.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Project Management Specialist - Agensys, Santa Monica, CA
The ideal candidate will have a university degree and a minimum of 5 ? 8 years related experience in Project Management or in Drug Development ? preferably both. Even more preferable would be Drug development project management experience in biologics or biologic-based drugs. Working knowledge of PM tools such as MS Project and MS Excel is required. Experience in initiating and implementing additional communication, planning, scheduling and development strategy software tools are a plus. Excellent communication skills and the ability to work in a team environment are essential. PMP certification a plus but not essential
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Principal Safety Scientist
Minimum of Bachelor?s Degree in Science or Pharmacy or Nursing required.Minimum of 5 years pharmaceutical experience in a clinical safety/research department required.Minimum of 5 years of medical writing experience (Prefer experience in writing pharmaceutical reports such as Clinical Study Reports, Safety sections of the ISS and/or EU Common Technical document, PSUR or white paper).Proven ability to critically evaluate medical data.Proven understanding of clinical disease state and implications of treatment.Proven ability to communicate effectively (verbal, presentation at group meetings, etc).Proven experience with project management (formal or informal).Prefer experience in training or mentoring.Strategic thinking, Organizational, Leadership, Results-oriented performance, Team player.Excellent knowledge of ICH, US & EU regulations and requirements for pharmacovigilance (experience with world-wide safety reporting regulations and guidelines Excellent interpersonal skills, including ability to work effectively cross culturally and cross functionally.Proven ability to effectively lead cross-functional teams with respect to risk management activities and to influence where direct reporting line relationships do not exist. Excellent written and spoken English
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
PET Senior Research Associate- Agensys, Santa Monica, CA
This position requires a Bachelor/Master?s Degree of Science and at least three years of direct animal research experience utilizing microPET/CT systems; an associates degree and Five years animal research experience with at least 3 years utilizing PET/CT; or eight years directly related animal research experience with 5 years utilizing PET/CT .AALAS certification at the LATG level is also required. The qualified individual must possess excellent organizational and communication skills, exhibit problem solving skills, as well as a desire to learn new techniques and train others in a team environment. This role also requires the individual to be "results-driven" with the ability to think through processes in order to improve efficiency and outcome of studies required.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Medical/Senior Medical Director, Pharmacovigilance- Oncology
SUPERVISORY RESPONSIBILITY: Directly supervises Assistant Medical Director(s), Associate Medical Director(s), and/or Medical Director(s) in the PSP Department.KNOWLEDGE & EXPERIENCE: Identify specialized knowledge needed to perform the position. The years of experience are not required. Note if the specific knowledge or skill is required, desirable, or a plus.MD degree, Pharmaceutical Industry experience in Pharmacovigilance and drug safety for at least five years, Team working, analytical skills, and flexibility are essential for this position.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Medical Director/Senior Medical Director, Oncology
M.D. degree or equivalent; Board Certified or Board Eligible in oncology highly desirableMinimum 6 or more years experience in the pharmaceutical industry or equivalent academic experience.Strong working-knowledge of regulatory procedures and guidelines (preferably global)Experience in P1-3 clinical development; prior EU/US regulatory filing experience expected.Holds others accountableStrong industry acumen, vision and perspective
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Medical Director, Product Safety & Pharmacovigilance
This position is responsible for strategies in pre and post marketing risk management, as well as keeping abreast of pharmacovigilance methods and trends in published literature and global regulations. Additionally responsible for strategies in monitoring and analysis of cumulative safety information on Astellas products. Responsible for drug safety crisis managementSpecific responsibilities include:Guides regulatory reporting including individual case safety reports (ICSRs), NDA annual report summary statements, and Periodic Safety Update Reports (PSURs)Guides adverse event coding, retrieval and analysis activities in drug safety and clinical trialsGuides reviews of safety sections of NDA submissionsPlans cumulative safety information analysis such as signal detection from company or public databases with data miningGuides safety updates of company core data sheet and local product labelsGuides pharmacoepidemiology projectsGuides crisis management on drug safetyGuides Risk Management Plans for specific productsGuides and coordinates preparation of ad-hoc benefit-risk assessment documentsGuides regulatory strategy and preparation of data related safety to regulatory authorities and advisory committeesInterfaces with Medical Sciences, Clinical Studies, Product Safety Management, Drug Development and Project Management, Pharmacoepidemiology, Global Pharmacovigilance departments, Toxicologist, Biopharmaceutical sciences, Research Data Sciences, Legal Demonstrated leadership skills and strategic focus. Demonstrated ability to exercise independent judgment and effectively collaborate with multiple functional unitsPosition requirements: MD degree, Pharmaceutical Industry experience in Pharmacovigilance and drug safety for at least five years, Team working, analytical skills, and flexibility are essential for this position
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Medical Director, Medical Sciences- Oncology
M.D. degree, Board Certified or Board Eligible in Oncology/Hematology.Minimum three years clinical experienceMinimum two years laboratory or clinical research experience and five years experience in the pharmaceutical industry or equivalent academic experience.Knowledge of regulatory procedures and guidelines (preferably global)Experience in clinical development, preferably experience in at least 2 phases Effective team player in a matrixed R&D environmentAble to work independently on all aspects of assigned projectsExcellent presentation and writing skillsExcellent organizational skills
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Manager/Senior Manager CMC Analytical Development - Agensys, Santa Monica, CA
PhD in chemistry, biochemistry or biology with 10+ years experience in development, qualification, and transfer of chromatographic, spectrophotometric, electrophoretic, and other relevant analytical methods for protein biotherapeutics in a biopharmaceutical environment. -hands-on experience and a good understanding of LC-MS and MS/MS for biologics is a must; the ability to troubleshoot complex technical and scientific problems; an in-depth understanding of protein characterization techniques: proven supervisory and managerial skills are essential; -a high level of expertise with cGMP, and regulatory compliance in biotechnology product development is expected; -experience with immunological methods is a strong plus; experience with analytical test method development for small molecular is preferable. Must be able to perform in a fast paced multiproduct environment.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Laboratory Manager - Agensys, Santa Monica, CA
EDUCATION: B.S./M.S. degree in Science.Experience: At least five years of Lab management experienceThe successful candidate must demonstrate a strong working knowledge of pharmaceutical/biotechnology research laboratories and their unique safety issues, including vivarium facilities and familiarity with IACUC regulations. Experience in industry is strongly preferred. Strong written and verbal communication skills, as well as interpersonal skills are also essential. In addition, the successful candidate must have the ability to demonstrate leadership and problem solving skills in a team based environment.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Global Development Project Leader - Central Nervous System
An MD, PhD or PharmD is preferable with a specialty in the CNS therapeutic area required along with experience in global development. Experience in the area of Alzheimer disease preferred. Total leadership experience including line/project management. multidisciplinary program management experience, which includes leadership in more than one IND/IMPD, NDA/MAA, Advisory Committee or other PMDA/EMEA/FDA meetings.Minimum of ten (10) years experience in drug development in pharmaceuticals, biopharmaceuticals, or biotechnology.Demonstrated experience leading the development of at least one development candidate with adherence to quality, excellence and efficiency.Demonstrated experience leading drug development projects and activities in a matrixed, global organization. A broad understanding of how to communicate and work well with team members and relevant people as well as scientists and external decision-makers worldwide. A thorough understanding of how to influence local and global regulatory, scientific and commercial environments.Skill Set:o Ability to assimilate data, recognize key variables and analyze complex situations. Make quality judgments.o Has a realistic expectation of the business, one?s self and others.o A style which builds alliances within the organization, locally/globally, and/or corporate collaborators.o Does not confuse effort for results.o Tenacity to weather short-term setbacks for long-term advantages.o Broad understanding of the multidisciplinary functions contributing to effective and efficient drug development.Solid understanding of CMC, pharmacology, toxicology, PK, clinical requirements to support major regulatory filings ? IND/IMPD, NDA/MAA.Leads preparation of PMDA/EMEA/FDA milestone meetings, such as Pre-IND, End-of-Phase II, Pre-NDA, Advisory Committees, focusing on the key strategic issues.Excellent understanding of the interdependencies of the various disciplines (CMC, Pharm/Tox, PK, Clinical, Regulatory, Marketing, Finance, etc) - what needs to be evaluated simultaneously vs. sequentially etc. from a strategic planning/risk management time/event/cost point locally and globally.Understanding of how to educate/advise others on Regulatory Guidances/Internal SOPs/PM concepts.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Director/Senior Director, Global Development Project Lead, Oncology
An MD, PhD or PharmD is preferable with a specialty in the assigned oncology area, or equivalent experience with global development required. Total leadership experience including line/project management. multidisciplinary program management experience, which includes leadership in more than one IND/IMPD, NDA/MAA, Advisory Committee or other PMDA/EMEA/FDA meetings.Minimum of ten (10) years experience in drug development in pharmaceuticals, biopharmaceuticals, or biotechnology.Demonstrated experience leading the development of at least one development candidate with adherence to quality, excellence and efficiency.Demonstrated experience leading drug development projects and activities in a matrixed, global organization. A broad understanding of how to communicate and work well with team members and relevant people as well as scientists and external decision-makers worldwide. A thorough understanding of how to influence local and global regulatory, scientific and commercial environments.Skill Set:o Ability to assimilate data, recognize key variables and analyze complex situations. Make quality judgments.o Has a realistic expectation of the business, one?s self and others.o A style which builds alliances within the organization, locally/globally, and/or corporate collaborators.o Does not confuse effort for results.o Tenacity to weather short-term setbacks for long-term advantages.o Broad understanding of the multidisciplinary functions contributing to effective and efficient drug development.Solid understanding of CMC, pharmacology, toxicology, PK, clinical requirements to support major regulatory filings ? IND/IMPD, NDA/MAA.Leads preparation of PMDA/EMEA/FDA milestone meetings, such as Pre-IND, End-of-Phase II, Pre-NDA, Advisory Committees, focusing on the key strategic issues.Excellent understanding of the interdependencies of the various disciplines (CMC, Pharm/Tox, PK, Clinical, Regulatory, Marketing, Finance, etc) - what needs to be evaluated simultaneously vs. sequentially etc. from a strategic planning/risk management time/event/cost point locally and globally.Understanding of how to educate/advise others on Regulatory Guidances/Internal SOPs/PM concepts.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Director, Translational Research - Agensys, Santa Monica, CA
Candidate consideration requires a Ph.D./M.D. with a minimum of 10 years of post-doctoral experience. Industrial experience in Oncology drug discovery and experience managing scientists is required. Successful candidates will have strong written and oral communication skills, be self-motivated, demonstrate leadership and possess an exemplary record of research, as evidenced by publications and patents.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Director, in vivo Pharmacology - Agensys, Santa Monica, CA
Candidate consideration requires a Ph.D. with a minimum of 10 years of post-doctoral experience. Industrial experience in Oncology drug discovery and experience managing scientists is required. Successful candidates will have strong written and oral communication skills, be self-motivated, demonstrate leadership and possess an exemplary record of research, as evidenced by publications and patents
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Cell Culture Associate - Agensys, Santa Monica, CA
? A B.S. or M.S. in biochemistry, biology, biochemical engineering or a related field. ? >3 years related experience in the biopharmaceutical/biotech industrial ? Prior hands-on experiences in cell culture process development, especially with shake flasks and bioreactors.? Operation experience with pilot-scale bioreactors will be plus ? Possess good problem solving, organizational, and documentation skills with a strong focus on details? Must have excellent organizational and communication skills? Must be highly motivated, be able to work independently as well as in teams
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Asst. Animal Technician/Animal Technician/Sr. Animal Technician - Agensys, Santa Monica, CA
Previous husbandry experience of laboratory rodents is highly desirableAn ALAT or higher certification and understanding of AAALAC accreditation are a plus. A BA/BS degree is a definite plusThe successful candidate must follow all animal health standards, stringent SOP?s and safety protocols, be able to lift objects of approximately 50 pounds and should have no allergies to common laboratory rodentsThe incumbent should have a general appreciation for biological science and an understanding of the intricacies of laboratory research.This person should have good verbal and written communication skills and the ability to work well in a team environment with a positive/can-do attitude.The person should also be detail-oriented and willing to work flexible hours.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Associate/Sr. Associate, Cell Line Development, Agensys, Santa Monica, CA
? The ideal candidates will have a B.S. or M.S. in Biology, Molecular Biology, Biochemical Engineering,or related field, with preferably a minimum of 2 years of relevant experience in industry.? Experience in generation of transient/stable cell lines and mammalian cell culture are required.? Working knowledge of antibody expression and detection in mammalian cells is preferred.? Compliance with appropriate written procedures; e.g. applicable safety, biological containment, and administrative procedures is required. ? Excellent written and oral communication skills and the ability to work in a team environment are essential.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Associate Manager, Outsourcing
Bachelors Degree in Business, Life Sciences or equivalent experience, Master?s Degree or other Advanced degree preferred.Generally 7 + years experience required in R&D Outsourcing, Clinical or Business Operations within a pharmaceutical company required.Strong analytical and problem solving skills and ability to come up with creative solutions.Strong team player.Demonstrated negotiation and influencing skills.Demonstrated ability to provide leadership.Demonstrated ability to strategically manage vendor relationships.Demonstrated ability to manage multiple projects simultaneously.Demonstrated ability to effectively communicate across all levels of management. Advanced use of word processing and spreadsheet software. Strong written and oral communications skills
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Associate Director, Quality Assurance - Agensys, Santa Monica, CA
1. Minimum BA / BS or equivalent, advanced degree preferred, with a minimum of 10 years of industry experience, 6 years of QA experience, and 3 - 5 years managing staff. 2. Comprehensive knowledge of GxP and other regulations and understanding of global quality standards relating to product development, submission and/or commercialization. Ability to contribute to local and global Quality policies in support of the quality system. 3. Effective written and oral communication and interpersonal skills, facilitation, and influencing skills with an demonstrated ability to lead projects, initiatives, or programs across multiple departments, regions and business units within Astellas group and external stakeholders. Demonstrated ability to solicit input and liaise with stakeholders to prioritize and set strategic direction for change. 4. Demonstrated ability to assess the state of current business and QA operations for Quality Systems to identify and recommend future state, improvements, and to implement action plans. 5. Demonstrated competence to resolve complex and diverse problems with decision making responsibility that has a major impact (e.g., stakeholder relationships, dossier approvals, compliance status, credibility and/or revenue) within QA and within the region. 6. Demonstrated experience developing quality strategies and priorities and translating them into short and long-term objectives for the department. Ability to provide leadership to Quality Systems programs, initiatives and teams, with minimal management oversight. 7. Demonstrated ability to develop quality assurance professionals and to both lead and manage a functional quality assurance unit.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Associate Director, CPED Science, Oncology
Minimum MS or equivalent qualification in a bio-medical/science field required. MD or PhD desired.The Assistant/Associate Director role requires at least 5-7 years post-graduate experience, in pharmaceutical industry, preferably from another (major) Pharma Company with a general understanding of Drug Discovery and Development. In addition, the individual should have the following experiences.Expert knowledge of disease biology and relevant clinical disease knowledge required to design early development strategies up to and including PoC.Expert knowledge of Clinical Pharmacology Knowledge and proven development expertise in at least 3 therapeutic areas.Team player with strong written and communication skills to bring over and get acceptance for plans.Strong, critical analytical mindOperate with minimum of supervision.Key organizer and planner who clearly sets priorities.Up to date with latest ICH-GCP guidelines and other relevant regulations.Highly developed sense for ethical conduct of Clinical Development
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Associate Director, Clinical Pharmacology - Agensys, Santa Monica, CA
? PhD, PharmD, MS, BS in Pharmacy or life sciences with extensive training in pharmacology, pharmacokinetics, and pharmacodynamics and data analysis -- also beneficial to have experience with population PK/PD modeling and simulation? 8-10 years of Phase I clinical trial experience or equivalent? 5 years of experience with oncology drug development? 5 years of experience with antibodies ? Knowledge of global drug development process and ability to design and implement development plans? Extensive experience in representing Clinical Pharmacology to regulatory agencies ? Established leadership skills? Proven communication, management and leadership skills
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Associate Director / Director Statistics
MS or PhD in statistics or mathematics; minimum of 7-10 years in pharma or CRO industry, with minimum of 2-4 years in functional or project management roleAt least 2 years experience in working on global clinical studies and projects or global process and system initiativesVery good understanding of all phases of clinical development, and processes in data scienceExperience in all aspects of statistics for clinical trials, and in working as a member of a project team including design of clinical studies and contribution to Clinical Development PlansExperience as lead statistician for multiple submissions to health authorities, substantial experience in interations with health authoritiesGood understanding of the various functions and expert groups contributing to Drug Development Solid knowledge of SAS and other statistical toolsMinimum requirements for Director level:Generally a minimum of 10 years of relevant experience in pharma or CRO industryMinimum of 4-5 years of management experience including 2-3 years in a line management positionDemonstrated ability to translate strategic plan for GDO, Data Science and Statistics into goals and objectives for own functionDemonstrated leadership skills and ability to effectively prioritize own group?s activities for development projects and clinical trialsProven ability to establish operating guidelines and procedures, preferably in a global settingDemonstrated ability to successfully identify and lead global process or system improvement initiatives
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Associate Biostatistics Director, Oncology
M.S. or Ph.D. in statistics or equivalentRequired proven oncology experience Minimum of 8 years experience in applying statistical methods in biomedical research, extensive pharmaceutical or CRO experience requiredExperience in working on clinical project teams. Good understanding of entire drug development process - ability to see the ?big picture?.Experience as the independent lead statistician in a regulatory submission preferredExperience with cross functional process improvement or innovation initiativesAdvanced and broad knowledge of statistical methods, along with understanding of industry practices related to the statistical analysis of clinical dataKnowledge and skills in SAS required and knowledge of other statistical software preferred.In-depth familiarity with processes and procedures in data management and SAS programmingExperience working in an international environment and demonstrated ability to manage and influence across different locations, time zones and cultures; builds global relationships. Ability to work in a matrix environment. Proven excellent organizational, project and time management skills.Leadership skills and ability to delegate appropriately and provide direction to more junior Biostatisticians. Very good oral, written, and presentation communication skills. Able to clearly communicate statistical issues and methods to both statisticians and non-statisticians. Very good problem solving skills.Accurate with a keen eye for detail. Dedication to quality and reliability in all work tasksAbility to perform under pressure
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Analytical Associate/Sr. Analytical Associate, Process Development - Agensys, Santa Monica, CA
The successful candidate will possess the following qualifications.? B.S. or M.S. in biochemistry, chemistry, or related field with at least three-year experience inbiotechnology/biopharmaceutical industry.? Experience in protein analysis by HPLC, gel electrophoresis, UV/Vis spectroscopy, and plate-basedprotein assays such as BCA and ELISA. Experience in CE and DSC is a plus
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
: Senior Scientist/Scientist, Applied Molecular Biology - Agensys, Santa Monica, CA
The successful candidate will have a PhD in molecular biology, biotechnology, biochemistry or related discipline with minimum 7 years of relevant industry experience. Other required experience includes expertise in a broad range of molecular and cellular techniques surrounding aspects of microarray-based discovery for biomarker and pathway identification, and knowledge of computational analysis of large data sets. Industrial experience in oncology drug discovery is preferred. Successful candidate will have excellent verbal and communication skills, demonstrate leadership and ability to work in a dynamic team environment.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Director / Senior Director, Discovery - Agensys, Santa Monica, CA
? Advanced degree (Ph.D., or equivalent) with at least 10 years? experience in an industry setting in Drug Discovery and related areas with an emphasis on target discovery and validation, and monoclonal antibody discovery and engineering. ? Strong background in Oncology drug discovery, evidenced by involvement in development of product candidates from initiation to clinical stage, some experience with biologics is preferred.? Demonstrated record in driving scientific and technical innovations, as evidenced by first or senior authored publications in top-tiered journals.? Demonstrated successful program leadership and multi-project coordination. ? At least 5 years of management experience of multiple groups. ? Proven track record in leading programs to achieve goals and timelines.? Ability to perform successfully in a cross-functional team environment.? Excellent written and verbal communication skills.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Associate Director, Regulatory Affairs
KNOWLEDGE & EXPERIENCE: ? Bachelor?s degree in scientific discipline; advanced degree preferred.? 9 years previous pharmaceutical drug development experience, 2 in managing staff.? Recognized as an expert in regulatory aspects of pharmaceutical drug development involving undefined frameworks with technical complexity and broad scope.? Scientific knowledge in chemistry, general biological/physical science and ability to apply that knowledge to regulatory issues and product development. Recognized as an expert in an aspect of pharmaceutical drug development. ? 6 years regulatory affairs experience preferably involving direct contact with the FDA; full knowledge of FDA and ICH regulations and guidelines, and the ability to provide interpretations of that information to others. Proven record of successful IND/NDA submissions and negotiations with the FDA in areas of CMC and product formulations. Regulatory experience in other therapeutic areas such as medical devices or biologics.? Strong organizational skills with the ability to manage large projects and provide regulatory guidance/training to direct reports and others in the department as needed.? Proven ability to prioritize and multi-task with minimal supervision based on interactions with project team members.? Ability to communicate effectively and maintain effective working relationships. Must be able to positively influence department staff and other APGD groups.? High integrity with respect to maintenance of proprietary, confidential information. ? Excellent written and oral communication skills, with writing ability to meet regulatory requirements and standards.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Director, Quality Systems
Minimum BA / BS or equivalent, advanced degree preferred, with a minimum of 10+ years of industry experience, 8 years of QA experience, and 4 ? 6 years managing staff.Experience in managing a Quality System within a GCP / Pharmacovigilance environment. Comprehensive knowledge of GxP and other regulations and understanding of global quality standards relating to product development, submission and/or commercialization. Establishes local and regional Quality policies in support of the quality system.Effective written and oral communication and interpersonal skills. Influencing skills with a demonstrated ability to lead projects, initiatives, or programs across multiple departments, regions and business units within Astellas group and external stakeholders. Demonstrated ability to solicit input and liaise with stakeholders to prioritize and set strategic direction for change.Demonstrated ability to assess the state of current business and QA operations for Quality Systems to identify and recommend future state, improvements, and to implement action plans.Demonstrated competence to resolve complex and diverse problems with decision making responsibility that has a major impact within QA and/or with functional groups within the region.Demonstrated experience leading strategic development and successful execution of plans and initiatives for addressing complex and diverse QA matters with minimal management oversight. Contributes to the identification and implementation of long-term business planning strategies, assuring quality is taken into consideration. Demonstrated ability to develop quality assurance professionals to both lead and manage a functional quality assurance unit.Demonstrated experience in hosting and facilitating regulatory agency inspections with successful outcomes.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Director Quality Assurance - Agensys, Santa Monica, CA
1. Minimum BA/BS degree with 8 years experience in Quality and 4 years managing staff and 10+ years in the pharmaceutical industry. 2. Comprehensive knowledge of GCP , GLP, and GMP and other regulations relating to product development, testing, submission and commercialization.3. Ability to contribute ideas for strategies and tactics to ensure adequate long term planning for the quality assurance function.4. Ability to establish standards in support of the quality system and to interface across multiple departments and levels of management.5. Practical experience of line management position while demonstrating a desire for creative, hands-on approach to leadership in support of a fast growing organization.6. Effective project management skills and commitment to meeting deadlines and work well under pressure.7. Excellent written and oral communication, facilitation and influencing skills with an ability to work within an environment which utilizes both in-house and out-sourced (contract/temporary) resources.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Associate Director, Quality Assurance, R&D Programs, GCP
Minimum BA / BS or equivalent, science-related preferred, with 10 years of industry experience, 6 years of QA experience, and 3-5 years managing staff.GCP Quality Assurance experience required and experience in a pharmaceutical manufacturing or clinical development environment preferred. Comprehensive knowledge of GCP regulations and understanding of global quality standards relating to product development, submission and/or commercialization. Demonstrated ability to establish local and regional Quality policies and to contribute to global Quality policies in support of the quality system.Ability to assist or lead strategic development and/or successful execution of plans and initiatives that ensure long term success for R&D Programs GCP at a Regional or Global level with minimal management oversight. Demonstrated accountability to resolve complex and diverse problems with decision making responsibility that has a significant impact (e.g., stakeholder relationships, dossier approvals, compliance status, credibility and/or revenue) within QA and across the APGD.Demonstrated ability to anticipate, proactively respond to trends, and/or shifts in the external environment (e.g., regulatory, business partner relationships, industry standards) and to predict impact on quality assurance and/or Astellas business units.Effective written and oral communication and interpersonal skills, facilitation, and influencing skills with an ability to interface regionally across multiple departments, and among various levels of management within Astellas group and external stakeholders. Demonstrated ability to solicit input and liaise with stakeholders to prioritize and set strategic direction for change. Assist in the identification and implementation of short and long-term business planning strategies, assuring quality is taken into consideration.Demonstrated ability to develop quality assurance professionals and to both lead and manage a functional quality assurance unit.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Assistant Director, Quality Systems
Minimum BA / BS or equivalent, advanced degree preferred, with a minimum 10 years of industry experience, 6 years of QA experience, and 3-5 years managing staff.Comprehensive knowledge of GxP and other regulations and understanding of global quality standards relating to product development, and commercialization. Ability to contribute to local and global Quality policies in support of the quality system.Effective written and oral communication and interpersonal skills, facilitation, and influencing skills with an demonstrated ability to lead projects, initiatives, or programs across multiple departments, regions and business units within Astellas group and external stakeholders. Demonstrated ability to solicit input and liaise with stakeholders to prioritize and set direction for change.Demonstrated ability to assess the state of current business and QA operations for Quality Systems to identify and recommend future state, improvements, and to implement action plans.Demonstrated competence to resolve complex and diverse problems with decision making responsibility that has a major impact (e.g., stakeholder relationships, dossier approvals, compliance status, credibility and/or revenue) within QA and within the region.Demonstrated experience developing quality strategies and priorities and translating them into short and long-term objectives for the department. Ability to provide leadership to Commercial Products and GMP programs, initiatives and teams, with minimal management oversight. Demonstrated ability to develop quality assurance professionals and to both lead and manage a functional quality assurance unit.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Assistant Director Marketing Analytics - IL, Deerfield
?X Bachelor��s degree is required, Master��s degree preferred, preferably in business or the sciences.?X Must have a minimum of 7-10 years successful experience in the pharmaceutical or other related healthcare field in the area of market research and analysis.?X Extensive computer proficiency with desktop software in a Windows environment required: Microsoft Word; Microsoft Excel; Power Point required, Microsoft Access; Cognos; Spotfire; and other Statistical software a plus.?X Excellent skills in the following areas: organization, written and verbal communication, accuracy and personal initiative.?X Must have a minimum of 1-3 years supervisory experience.?X Experience in forecasting, market model development is a strong positive.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Associate Marketing Director, Latin America
? 7-10 years of experience? Infectious Disease/Oncology experience.? English/Spanish required. Portuguese desirable.Required Qualifications:1. Bachelor's degree in a related discipline with an advanced degree in business. Science degree preferred. Marketing experience in specific therapeutic area may be required.2. 10+ years of relevant experience depending on degree, including 5 years marketing leadership experience within the Pharmaceutical industry.3. Global and regional marketing experience required preferably in Latin America.4. Requires significant communication and leadership skills and the ability to create and implement the Marketing Plan and integrate it with APLA objectives.5. Strong relationship management and influencing skills and comfort working with cross-functional teams.6. Excellent oral and written communication skills. Ability to understand and help define business questions and present findings in a compelling manner to various audiences.7. Ability to travel domestically and internationally required (up to 50%).8. Fluent in Spanish/English with Portuguese highly desirable.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Manufacturing Associate II, Bioprocess -- Agensys, Santa Monica, CA
BS in biological or other science related field and 3+ years relevant industrial experience in the manufacture or development of FDA regulated Biological Products. Clinical or commercial manufacturing experience preferred. Broad based technical knowledge with manufacturing equipment (i.e. Bioreactors, filtration, mixers, purification etc.). Excellent organizational skills, written and oral communication skills and ability to multi-task. Must possess mechanical aptitude.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Manufacturing Associate II, Bioprocess - Agensys, Santa Monica, CA
BS in biological or other science related field and 3+ years relevant industrial experience in the manufacture or development of FDA regulated Biological Products. Clinical or commercial manufacturing experience preferred. Broad based technical knowledge with manufacturing equipment (i.e. Bioreactors, filtration, mixers, purification etc.). Excellent organizational skills, written and oral communication skills and ability to multi-task. Must possess mechanical aptitude.
Astellas Pharma, Inc.	Oklahoma City	OK	9/9/2010
Manager, Engineering
? BS in chemical or mechanical engineering or equivalent relevant pharmaceutical science field required. Advanced degree preferred.? A minimum of 5 ? 8 years experience in solid dosage pharmaceutical manufacturing including packaging required.? A minimum two years management of engineers experience required.. ? Additional knowledge in at least one of the following areas is beneficial: Statistical Inference, SPC, Process Capability, DOE, Sampling plan or Risk Assessment.? Must be able to read, write and understand the English language (statement common to all Job Descriptions) ? Must be able to work to meet deadlines, and utilize problem solving skills. Must be able to gather and evaluate complex data to make effective decisions to accomplish work. Strong communication, prioritization and organizational skills. Attention to detail required. Ability to work independently and as a team member. Accurate record keeping.? Minimum supervision required
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Facilities Department Planner/Assistant- Agensys, Santa Monica, CA
? An Associates of Arts degree? A minimum of two years experience working in a pharmaceutical FDA regulated environment? A working knowledge of Computerized Maintenance Management Systems? Self-starter with the ability to work with minimum supervision? Excellent verbal and written communication skills? The ability to multitask and exercise good judgment? The ability to work in a fast pace environment and maintain a high level of customer service? Detailed oriented with good follow-up skills? Proficient in computer usage with standard business software
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Sr. Manager, Network & Security
10+ years broad Information Technology experienceProven leadership skills and a passion for operations excellenceRequires an in-depth understanding of networking and security technology including routers, routing protocols, firewalls, switches, intrusion detection and prevention systems, DLP, VPN, wireless and endpoint protectionExcellent project management, analytical and organizational skillsStrong problem solving and troubleshooting skillsStrong written, verbal and presentation skillsCCIE, CISSP, and ITIL certifications are a plusBachelor?s degree or equivalent
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Sr. Manager, Information Management
10+ years broad Information Technology experience5+ years direct IT experience in:Data & Information Architecture developmentConceptual and strategic IT planning and developmentData Warehouse Project ManagementIBM Infosphere and Cognos suite of productsSAP BW and Business Objects product suite Other significant experience in:Building and managing high performance teamsDeveloping strong partnerships with internal business groupsBuilding IT practicesData modelingDatabase toolsReporting toolsExcellent verbal and written communication skillsExcellent problem solving and analytical abilityIT degree or equivalent experienceProven track record of exceptional success
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Sr. Analyst, IT Quality
Bachelor?s Degree in Computer Science, related field, or equivalent experience required.5 + years relevant experience related to change management, document development, and application testing.Working knowledge of computer systems validation processes, system development life cycle, and Change Management processes. Must exhibit creativity and innovation in solutions; be broadly focused and able to manage multiple efforts concurrently.Exceptional attention to details and ability to consistently produce high quality and accurate work.Has solid interpersonal and communications skills (written, oral, and non-verbal) to effectively relate to technical staff and business customers.Ability to be self-directed within the scope of their duties and responsibilities.Ability to build and maintain positive and cooperative working relationships by demonstrating collaborative behaviors and cross functional facilitation skills.Understand the pharmaceutical industry and IT best practices.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Senior Director, IT Client Relationship Management
Serves as the IT liaison for a specific enterprise wide business unitManages the IT resources dedicated to the business unit or functionWorks directly with the senior leadership of the business unit and IT Performs or directs high level activities with appropriate awareness of other activities within the organizationServes as a business advocate to IT and an IT advocate to the businessResolves complex business issues that affect cross functional areas or multiple sitesDirects the IT application and support requirements from a staffing perspectiveKeeps the Business and IT informed of important changes in each of the respective areas Leads complex business process reengineering projects Controls project priorities and ensures balance between business needs and IT resource constraintsResponsible for project delivery, providing ongoing updates and advocacy to the Business and IT Meets regularly with business personnel to define, review or revise:IT support strategiesApplication portfolioProject priorities and statusSystems supportApplications and infrastructure service levelsApplication growth projections and new access requirementsDirects the development and documentation of IT Strategies and Plans as a member of the IT Senior Management TeamWorking jointly with key business contact(s), manages the IT budgets, projects and prioritiesExtensive knowledge and skill through broad and/or deep experiences in Pharma IT Strong communication and interpersonal skills, capable of motivating and influencing teamsPerform at the highest levels and able to make decisions on their ownAble to translate between technical and business leaders at the highest levelsViewed as credible, and well respected by the business and IT organizationsAccountability in building and maintaining positive and cooperative working relationships Fifteen or more years of relevant experience within the pharmaceutical industry Collaboration and cross functional facilitation skillsHigh level understanding of project management, quality assurance, and IT best practicesProficiency with commercial applications that are designed to support enterprise wide business capabilitiesAdvanced Degree required (or progress towards and significant industry experience)
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Associate Director, Global Strategy IT Projects
Bachelors Degree required. Advanced degree (masters, doctorate) a plus. Generally, ten plus (10+) years relevant IT experience or equivalent proven project management experience in an IT capacity within the pharmaceutical, biopharmaceutical, or biotechnology industries. Global experience preferred.Proven history of successful program management experienceA key organizer who has shown to set clear priorities on developmental activities and finances with experience in financial reporting and planning systems. A demonstrated leader in a matrix organization, able to motivate and inspire local team members to high performance levels.Good communication, people management and social skills with a good sense of diplomacy both in an IT and other environments.Excellent understanding of the interdependencies of the various disciplines (e.g. R&D, Legal, HR, Supply Chain, Marketing, and Finance). This will include an understanding of what needs to be evaluated simultaneously vs. sequentially from both a local and a global project management perspective.Understanding of how to educate/advise others on IT/Internal SOPs/PM concepts
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Associate Director, Human Resources
Bachelor?s degree in Human Resources or Business, or equivalent experience required. Master?s degree preferred.Seven to ten years related experience required, preferably in the pharmaceutical or healthcare industries. Three to five years management experience required.Demonstrated Human Resources generalist knowledge required, specifically including employment law.Incumbent must have demonstrated ability to work in a challenging, multi-cultural work environment.Ability to manage confidential information imperative, including influencing others to maintain the confidentiality of sensitive information.Some travel required, up to 50% depending on assigned organizations.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Associate Director, Compensation
Minimum of 10+ years of experience in human resources with at least seven years compensation experience. Experience in the pharmaceutical industry preferred. Requires Bachelors Degree, MBA preferred.Excellent knowledge of HR/compensation practices and principles, and all applicable labor, pay, benefits, health and safety laws and regulations. Excellent, planning, time management, communication, decision-making, presentation, organization, and interpersonal skills.Strategic business partner, good communicator with excellent interpersonal skills. Ability to communicate and present information to all levels within and outside the organization in a comprehensible manner. A team player with outstanding leadership skills. Detail oriented and accurate. Proactive. Solid mathematical aptitude and analysis skills. Knowledge of human resources automated systems. Work requires professional written and verbal communication and interpersonal skills. Ability to motivate teams to produce quality materials within tight timeframes and simultaneously manage several projects.
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Senior Maintenance Mechanic - Agensys, Santa Monica, CA
? A High School Diploma? Ten years relevant experience in Bio-Pharmaceutical, petrochemical, packaging or power generation industries with at least four years of that in a pharmaceutical FDA regulated GMP environment ? Demonstrated abilities and /or evidence of training in the repair, operations and troubleshooting of electromechanical process equipment, HVAC systems and utility systems? The ability to read blueprints and P&ID?s? Good communication skills verbal and written? Good computer and keyboard skills, proficient with standard business software
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Sr. Manager, Clinical Studies, Oncology
University/College degree with seven years clinical trials experience is desired. Proven time and project management skills, knowledge of drug development process and proven leadership ability is required. Working knowledge of ICH and GCP guidelines is required. Experience in people management is preferred.Proven track record in oncology required. Must have excellent interpersonal, written and verbal communication skills, administrative skills and computer ability. Travel required.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Senior Manager/Associate Director, Clinical Study Management Support
Minimum requirements of Senior Manager level:BA/BS degree with at least 7 years of clinical trial management and/or clinical document management experience; advance degree preferred (MS/PhD) with at least 5 years clinical trial and/or clinical document management experience.Minimum of 2 years of people management experience.Must have expertise in implementing operational strategies and strong knowledge of ICH/GCP guidelines and regulatory requirements.Must have detailed understanding of the clinical research and drug development process and experience handling associated documents.Must have strong computer skills and knowledge of information and document management systems.Must have proven and effective interpersonal, leadership, written and verbal communication skills.Fluent in English; minimal (<10%) travel required.Minimum requirements for Associate Director level:BA/BS degree with at least 10 years of clinical trial management and/or clinical document management experience; advanced degree preferred (MS/PhD) with at least 7 years clinical trial and/or clinical document management experience.Minimum of 4 years of people management experience.Must have extensive experience in implementing operational strategies and strong knowledge of ICH/GCP guidelines and regulatory requirements.Demonstrated ability to translate strategic plan for GDO and Clinical Site and Document Management into goals and objectives for function.Demonstrated leadership skills and ability to effectively prioritize own group?s activities for development projects and clinical trials.Proven ability to establish operating guidelines and procedures, preferably in a global setting.Demonstrated ability to successfully identify and lead global process or system improvement initiatives.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Senior Manager, Clinical Studies
University/College degree with seven years clinical trials experience is desired. Proven time and project management skills, knowledge of drug development process and proven leadership ability is required. Working knowledge of ICH and GCP guidelines is required. Experience in people management is preferred. Must have excellent interpersonal, written and verbal communication skills, administrative skills and computer ability. Travel required.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Senior Director, Statistics & Clinical Programming
Minimally a PhD in Statistics, or equivalent Degree, with specialization in Pharmaceutical Drug Development or equivalent work experience. Must have at least 10-15 years of pharmaceutical industry experience specifically in human drug development, and at least 3-5 years managing managers within a biometrics, biostatics function in clinical development. Preferably, will have successfully led a global Biostatistics and Programming function in a major pharmaceutical company. Must have a successful track record in the hiring and retention of excellent statistical and data management scientists who work optimally in a cross functional team and matrix environment. Must have a successful track record in effectively collaborating with other functions in development, discovery research, Medical Affairs and Commercial in the development and support of medicines. Must have an in-depth personal experience and understanding of the relevant expert groups within the Statistics and Programming function and their critical contribution to drug development. Must also have an understanding of the functions of multiple business units throughout the company, and have maintained effective collaborations with leadership of those business units and functions. Is considered an industry expert and is able to recognize the implications of new directions, trends and developments in the area of design, acquisition and reporting of data in the pharmaceutical industry. Must have extensive knowledge of the application of statistical analysis and reporting tools. Must be a strong and effective strategic thinker and problem solver, requiring the ability to both recognize and anticipate problems, and also help managers and individuals develop their own problem solving skills and discipline. However, must also be able to identify and solve tactical problems and delve into high degree of detail when necessary. Plans for and has detailed knowledge of all available resources internally and externally, has developed the appropriate relationships with partners and vendors, and has the ability to marshal those resources in a productive and efficient manner, either as part of a 3 year strategic capacity plan, or when there is need for sudden and immediate change in direction.Displays the highest level of personal commitment to the Astellas code of Ethics. Is exemplary in ensuring that "every employee deserves a great manager". Inspires while holds all appropriately accountable. Commits through co-accountability, to the growth and health of GDO, APGD and Astellas.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Senior Director, Global PK Modeling & Simulation
PhD in Life Sciences required. Must have at least 10 or more years of pharmaceutical industry experience, specifically in global human drug development, both in exploratory development, late clinical pharmacology and later phases of development. Broad therapeutic area knowledge and prior experience with biologicals is important. Extensive knowledge experience in application of PKMS in global drug development, both in Exploratory Development as wel as late CP. Good understanding of Late Development as well as Drug Discovery.Good knowledge of mathematics and power of mathematical modelsMust have a successful track record in interactions with Global Regulatory authorities; prior experience contributing to successful regulatory filings highly important. Must have a successful track record in the hiring and retention of excellent scientists who work optimally in a cross functional team and matrix environment. Must have a successful track record in effectively collaborating with other functions in development, discovery research, Medical Affairs and Commercial in the development and support of medicines. Displays the highest level of personal commitment to the Astellas code of Ethics. Is exemplary in ensuring that "every employee deserves a great manager". Inspires while holds all appropriately accountable. Commits through co-accountability, to the growth and health of GCPED, APGD and Astellas.Must have an in-depth personal experience and understanding of the GCPED function and its critical contribution to drug development. Must have extensive experience in interactions with global Regulatory Authorities. Must also have an understanding of the functions of multiple business units throughout the company, and have maintained effective collaborations with leadership of those business units and functions. Is considered an industry expert and is able to recognize the implications of new directions, trends and developments as it relates to GCPED and Astellas business. Must be a strong and effective strategic thinker and problem solver, requiring the ability to both recognize and anticipate problems, and also help managers and individuals develop their own problem solving skills and discipline. However, must also be able to identify and solve tactical problems and delve into high degree of detail when necessary. Plans for and has detailed knowledge of all available resources internally and externally, has developed the appropriate relationships with partners and vendors, and has the ability to marshal those resources in a productive and efficient manner, either as part of a 1-3 year strategic capacity plan, or when there is need for sudden and immediate change in direction.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Senior Director, Clinical Study Management
Minimally a BS. Must have at least 10 years of pharmaceutical industry experience specifically in human drug development, and at least 3-5 years managing managers of Clinical Study Managers in multiple therapeutic and geographic areas. Must have a successful track record in the hiring and retention of excellent clinical operations resources globally, who work optimally in a cross functional team and matrix environment. Must have a successful track record in effectively collaborating with other development functions in the development and support of medicines. Must have an in-depth personal experience and understanding of the Clinical Science function and the critical contribution of Clinical Operations to drug development, Must also have an understanding of the functions of multiple business units throughout the company, and have maintained effective collaborations with leadership of those business units and functions. Is considered an industry expert and is able to recognize the implications of new directions, trends and developments globally and on a multi-country and regional level, in site and patient recruitment, site monitoring, essential document collection and management, and the optimal use of cross functional outsourcing relationships. Must be a strong and effective strategic thinker and problem solver, requiring the ability to both recognize and anticipate problems, and also help managers and individuals develop their own problem solving skills and discipline. However, must also be able to identify and solve tactical problems and delve into high degree of detail when necessary. Plans for and has detailed knowledge of all available resources internally and externally, has developed the appropriate relationships with partners and vendors, and has the ability to marshal those resources in a productive and efficient manner, either as part of a 3 year strategic capacity plan, or when there is need for sudden and immediate change in direction.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Clinical Research Specialist
University/College Degree or previous healthcare experience desired. Must have excellent interpersonal, written and verbal communication skills, administrative skills and computer abilities. Minimum travel required.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Associate Director, Clinical Studies
B.S./B.A. life sciences degree or B.S.N or R.N. and ten years clinical research experience with four years experience in the management of people; M.S. degree and seven years related clinical research experience with four years people management experience; Pharm. D. or Ph.D. degree and five years of clinical research experience and a minimum of four years managing people. Must have excellent interpersonal skills, written and verbal communication skills, administrative skills and computer ability as well as in depth knowledge of the clinical drug development process and clinical study design and planning. He/she must be able to rapidly grasp medical concepts in a variety of therapeutic areas. Experience in project management and strategic planning is preferred. Ideal candidate will have managed a project leading to a New Drug Application or Product License Application. Candidate must also have proven management and leadership ability, knowledge of FDA/GCP requirements and familiarity with the pharmaceutical industry. Moderate (20-40%) travel required.
Astellas Pharma, Inc.	Deerfield	IL	9/9/2010
Associate Director / Director, Clinical Study Management
BA/BS degree with at least 10 years clinical trial management experience; advanced degree (MS, PhD, PharmD) preferred with 7 years clinical trial management experienceMinimum of 4 years people management experienceMust have extensive expertise in developing operational strategies and strong knowledge of ICH/ GCP guidelines and multinational clinical trial regulations.Must have extensive experience in people and project management, strategic planning and a strong knowledge of protocol and clinical drug development processes, clinical study design, study planning and management.Must have experience working across multiple molecules, indications and phases of development. Must have proven and effective interpersonal, leadership, written and verbal communication skills, administrative skills and computer ability. Fluent in English; low to moderate (5% to 20%) travel required.Minimum requirements for Director level:BA/BS degree with at least 12 years of clinical trial management experience; advance degree preferred (MS/PhD/PharmD) with at least 8 years clinical trial management experienceMinimum of 6 years of people management experienceDemonstrated ability to translate strategic plan for GDO and Clinical Science into goals and objectives for functionDemonstrated leadership skills and ability to effectively prioritize own group?s activities for development projects and clinical trialsProven ability to establish operating guidelines and procedures, preferably in a global settingDemonstrated ability to successfully identify and lead global process or system improvement initiatives
Astellas Pharma, Inc.	Santa Monica	CA	9/9/2010
Financial Analyst - Agensys, Santa Monica, CA
? B.S, degree in a Accounting or business preferred.? 3 to 6 years of financial data analysis experience.? Excellent skill in manipulating Excel spreadsheets.? Ability to develop meaningful reports from complex data sources.? Strong knowledge of GAAP.
Daiichi Sankyo, Inc.	Terre Haute	NJ	9/9/2010
Sales Representative, Primary Care 3 - Terre Haute, IN
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Houston	TX	9/9/2010
Sales Representative, Primary Care 3 - Houston West, TX
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Edison	NJ	9/9/2010
Project Data Manager
Education/Experience Qualified canddiates must have a Master's degree; Bachelors degree or registered nurse in life sciences; 4 to 6 years (MS) pharmaceutical/data management; 6 to 8 years (BS/RN) pharmaceutical/data management. Project management experience is preferred. Demonstrated knowledge of clinical data flow and research design; clinical database administration and system validation experience; demonstrated competence with GCP/regional regulatory guidelines, SOPs (including WPs), medical terminology, standard coding dictionaries, and demonstrated proficiency in applying them to all relevant therapeutic areas and CRO management experience, including a thorough knowledge of CRO audits are critical skills in this role. EDC and SDTM experience is preferred.
Daiichi Sankyo, Inc.	New Haven	CT	9/9/2010
Sales Representative, Primary Care 3 - New Haven, CT
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred
Daiichi Sankyo, Inc.	Santa Barbara	CA	9/9/2010
Specialty Sales Representative - Santa Barbara, CA
Requirements: BS/BA Degree. Two or more years of pharmaceutical sales experience.
Daiichi Sankyo, Inc.	Parsippany	NJ	9/9/2010
Sr. Director Operational Excellence
Education/Experience Qualified candidates must have a Bachelor’s Degree in Life Sciences, Chemical, Biochemical Engineering or related field; Master’s or Ph.D. preferred. Minimum of 10 years overall work experience with a a minimum of 6 years management experience in the pharmaceutical, biotech or analytical contract laboratory industries. Experience should include process development, manufacturing operations, fill/finish production support, process transfer, scale-up and troubleshooting. Management experience should include Stability, QC, Analytical R&D, direct supervision of technical staff, direction of laboratory operations, and implementation of process and system improvements. Must have strong record of managing and delivering global, cross-functional projects across multiple technologies. Skilled in transitioning support from one team to another. Knowledge of Quality by Design (QBD) and Process Analytic Technology (PAT) and demonstrated ability to apply technology solutions to business problems are required skills in this role. Strong knowledge of regulatory requirements and guidance—particularly cGMPs and a thorough understanding of SAP reporting functionality including standard and organization specific reports are required skills in this role. Active membership with ISPE, RAPS or BIO is highly desirable. Must be willing to travel 15% of the time domestically and internationally.
Daiichi Sankyo, Inc.	Manhattan	NY	9/9/2010
Specialty Sales Representative, Manhattan North, NY
Requirements: BS/BA Degree. Two or more years of pharmaceutical sales experience.
Daiichi Sankyo, Inc.	Columbus	OH	9/9/2010
Sales Representative, Primary Care 1 - Columbus South, OH
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Edison	NJ	9/9/2010
Director, Clinical Development
Education/Experience Qualified candidates must have a MD with training in Internal Medicine. Subspecialty training in Endocrine and Metabolism or related therapeutic area preferred. PhD or PharmD degree candidates with extensive clinical development experience will be considered. For MD, a minimum 2 years of hands-on industry experience in drug and clinical development is required. For PhD or Pharm. D, a minimum of 4 years of clinical development is required. Knowledge of pharmaceutical business, worldwide drug development and regulatory process are preferred. Expertise in complex clinical trial design (i.e. factorial design, etc.) and complex implementation (i.e. including Steering Committees, Safety Monitoring Boards, etc.) as well as the interpretation of scientific data. Independent thinking, creativity, self starting and innovation. Ability to deliver high quality products. Strong interpersonal skills and ability to interface effectively with multinational development teams in a multicultural working environment. Excellent communication, presentation and negotiation skills with emphasis on building consensus. Ability to effectively manage interactions with academic thought leaders ensuring optimal cooperation for achieving program and department goals. Ability to anticipate and facilitate issue resolution in a multicultural working and business environment.
Daiichi Sankyo, Inc.	Jacksonville	FL	9/9/2010
Sales Representative, Primary Care 2 - Jacksonville South, FL
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Columbus	OH	9/9/2010
District Manager, Primary Care 2 - Columbus, OH
Experience and Education Requirements: Bachelor's Degree required. Minimum 3 years Pharmaceutical sales experience. Previous management experience preferred. OR 4 years Pharmaceutical experience, with a minimum of 2 years sales experience and 2 years of home office experience (e.g. marketing, sales operations, sales training). Overnight travel up to fifty percent required.
Daiichi Sankyo, Inc.	Parsippany	NJ	9/9/2010
Manager, Managed Markets - Customer Value Marketing
Education/Experience Qualified candidates must have a bachelor's degree; master's degree is preferred. Minimum of 5 years of pharmaceutical experience is required. Minimum of 1 year of pharmaceutical sales experience; minimum of 2 years of pharmaceutical managed care sales and account management; and managed markets marketing experience, marketing research or brand marketing is preferred. Clear understanding of Managed Markets customers including customers’ views on pharmaceutical co-marketing, education, and partnering initiatives with pharmaceutical companies as well as financial P&L understanding, legal, regulatory, compliance, clinical guidelines, and disease management are critical skills in this role.
Daiichi Sankyo, Inc.	Manhattan	NY	9/9/2010
Sales Representative, Primary Care 2 - Manhattan S, NY
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Reading	PA	9/9/2010
Sales Representative, Primary Care 3 - Reading, PA
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Lafayette	IN	9/9/2010
Sales Representative, Primary Care 2 - Lafayette, IN
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Parsippany	NJ	9/9/2010
Project Data Manager
Education/Experience Qualified candidates must have a Bachelor's degree or Registered Nurse with a minimum of 6 years pharmaceutical/data management experience or a Master's degree plus a minimum of 4 years experience in pharmaceutical/data management. Project management experience is preferred. Clinical database administration and system validation experience; CRO management experience; and demonstrated knowledge of clinical data flow and research design are critical skills in this role.
Daiichi Sankyo, Inc.	Brooklyn	NY	9/9/2010
Sales Representative, Primary Care 2 - Brooklyn North, NY
Requirements: BS/BA Degree. Two or more years of pharmaceutical sales experience.
Daiichi Sankyo, Inc.	Johnstown	PA	9/9/2010
Specialty Sales Representative, Johnstown, PA
Requirements: BS/BA Degree. Two or more years of pharmaceutical sales experience.
Daiichi Sankyo, Inc.	seattle	WA	9/9/2010
Hospital Sales Representative, Seattle South, WA
Education and Experience Guidelines: Bachelor's Degree from an accredited four-year institution required; advanced degree desirable A total of 3 years of pharmaceutical sales experience; Cardiovascular and or Hospital experience preferred Broad healthcare market business acumen and industry knowledge. Outstanding verbal communication skills a must. Ability to self-motivate. Attention to detail. Must possess an executive presence.
Daiichi Sankyo, Inc.	Austin	TX	9/9/2010
Sales Representative, Primary Care 1 - Austin, TX Overhire
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Edison	NJ	9/9/2010
Director, Global Project Management
Education/Experience Qualified candidates must have a PhD degree preferred or other advanced degree (i.e., MS or MBA) with additional relevant experience. Minimum of 10 years experience in an R&D function within a biotech or pharmaceutical company with 5 years of pharmaceutical research and development project management experience, and an understanding of drug commercialization and marketing. Demonstrated experience motivating and leading project teams to completing all activities associated with managing product candidates through all stages of development and registration including submission of at least one major NDA/MAA or major supplemental regulatory submission. This includes coordinating integrated drug development plans, project team meeting minutes, and project schedules. Strong communication, negotiation, and computer skills. Working knowledge of Word, Excel, PowerPoint, and Project Management software applications. PMI or similar certification is a plus. Must be willing to travel 25% of the time.
Daiichi Sankyo, Inc.	Dallas	TX	9/9/2010
Sales Representative, Primary Care 1 - Dallas/Ft. Worth Overhire
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Rocky Mount	NC	9/9/2010
Sales Representative, Primary Care 3 - Rocky Mount, NC
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Salina	KS	9/9/2010
Sales Representative, Primary Care 1 - Salina, KS
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred
Daiichi Sankyo, Inc.	Chicago	IL	9/9/2010
District Manager, Hospital Sales - Chicago, IL
Education and Experience Guidelines BS / BA required Five years successful pharmaceutical sales experience. A minimum of two years district manager experience; Hospital Management and Cardiovascular experience is preferred. Must be able to travel to meetings and related sales events up to 50-70% of the time.
Daiichi Sankyo, Inc.	Pittsburgh	PA	9/9/2010
Sales Representative, Primary Care 1 - Pittsburgh West, PA
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Atlanta	GA	9/9/2010
Sales Representative, Primary Care 1 - Atlanta West, GA
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Parsippany	NJ	9/9/2010
Associate Director, HEOR Biostatistics
Education/Experience Qualified candidates must have an advanced degree in biostatistics or relevant field and a minimum of 5 years experience in the pharmaceutical industry or consulting organization. Ph.D. is preferred. Analytical experience in cardiovascular and oncology; and knowledge of cardiovascular and oncology therapeutic areas is preferred. Proficiency in data management across multiple platforms; expertise in using statistical software such as SAS and SPSS; and scientific computer programming, database querying, and descriptive and inferential statistics are required. Experience with economic modeling, multiple imputation techniques and truncated data analysis is preferred. Must be willing to travel 10% of the time.
Daiichi Sankyo, Inc.	Dallas	TX	9/9/2010
Sales Representative, Primary Care 2 - Dallas East, TX
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred
Daiichi Sankyo, Inc.	Worcester	MA	9/9/2010
Specialty Sales Representative,Worcester, MA
Requirements: BS/BA Degree. Two or more years of pharmaceutical sales experience.
Daiichi Sankyo, Inc.	Oceanside	NJ	9/9/2010
Sales Representative, Primary Care 3 - Oceanside, CA
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Oceanside	CA	9/9/2010
Sales Representative, Primary Care 1 - Oceanside, CA
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Chesapeake	VA	9/9/2010
Sales Representative, Primary Care 3 - Chesapeake, VA
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	New Orleans	LA	9/9/2010
District Manager, Primary Care 2 - New Orleans, LA
Experience and Education Requirements: Bachelor's Degree required. Minimum 3 years Pharmaceutical sales experience. Previous management experience preferred. OR 4 years Pharmaceutical experience, with a minimum of 2 years sales experience and 2 years of home office experience (e.g. marketing, sales operations, sales training). Overnight travel up to fifty percent required.
Daiichi Sankyo, Inc.	Fond du Lac	WI	9/9/2010
Sales Representative, Primary Care 3 - Fond du Lac, WI
Requirements: BS/BA Degree. Two or more years of pharmaceutical sales experience.
Daiichi Sankyo, Inc.	East Brunswick	NJ	9/9/2010
Sales Representative, Primary Care 2 - East Brunswick, NJ
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Parsippany	NJ	9/9/2010
Senior Director State Government Affairs
Education/Experience: Education/Experience: Qualified candidates must have a Bachelor's degree with a minimum of 7 years working in the pharmaceutical industry or with primary concentration in industry policy/legislative issues; 7 years lobbying experience at the state level of government. Graduate degree in Government Affairs, Public Policy or Law; minimum of 2 years of experience as the legislative director or health policy advisor for a federal or state legislator or Governor’s Office is preferred but not required. The incumbent must have 5 years or more experience managing others and must possess excellent knowledge of state legislative processes. Professional affiliation with the National Conference of State Legislatures and with industry trade associations including PhRMA, BIO, HINJ is preferred but not required. The incumbent is expected and must be able to engage in frequent overnight travel throughout the continental United States to carry out the above-referenced duties and responsibilities. It is imperative that the incumbent demonstrates a proactive, energetic, time-sensitive, results driven approach in carrying out all management and other duties, obligations, and responsibilities. Must be willing to travel 40% of the time.
Daiichi Sankyo, Inc.	Houston	TX	9/9/2010
Sales Representative, Primary Care 1 - Houston Medical Center, TX
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Wilkes Barre	PA	9/9/2010
Sales Representative, Primary Care 3 - Wilkes Barre, PA
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Parsippany	NJ	9/9/2010
Administrative Assistant, Information Systems
Education/Experience HS diploma required; Associate’s Degree or completion of secretarial vocational program preferred. 3-5 years secretarial experience is preferred. Qualified candidates must have strong organizational ability, effective time management, excellent customer service skills, and a detail-oriented work style. In addition, good oral and written communication skills are required as well as the ability to manage multiple tasks. Proficiency in MS Office (Word, Excel, PowerPoint) and Outlook are also required. Experience providing administrative support in IT and /or the pharmaceutical industry a plus.
Daiichi Sankyo, Inc.	Parsippany	NJ	9/9/2010
Director, Biostatistics and Data Management
Education/Experience Qualified candidates must have a MS in Statistics, Biostatistics, or Mathematics with a minimum of 15 years of pharmaceutical industry experience or a PhD in Statistics, Biostatistics, or Mathematics with a minimum of 10 years of pharmaceutical industry experience. Extensive experience analyzing clinical trial data; experience managing external contracted resources required; direct personnel management experience is preferred. The incumbent must have full knowledge of advanced statistical analytical methods, data management, clinical trial research, regulatory requirements, programming skills, and statistical software. Demonstrated mastery of advanced statistical analytical methods, competency in SAS, clinical trial search, regulatory requirements; coding techniques, protocol development and personal computing.
Daiichi Sankyo, Inc.	Pittsburgh	PA	9/9/2010
Hospital Sales Representative, Pittsburgh South, PA
Education and Experience Guidelines: Bachelor's Degree from an accredited four-year institution required; advanced degree desirable A total of 3 years of pharmaceutical sales experience; Cardiovascular and or Hospital experience preferred Broad healthcare market business acumen and industry knowledge. Outstanding verbal communication skills a must. Ability to self-motivate. Attention to detail. Must possess an executive presence
Daiichi Sankyo, Inc.	Parsippany	NJ	9/9/2010
Exec. Medical Dir Medical Research TA Head - Oncology
Education/Experience Qualified candidates must have a MD degree with a minimum of 10 years experience in oncology clinical, research or academic medicine and either a minimum of 7 years of pharmaceutical industry experience or 15 years experience in academic medicine with experience conducting industry sponsored trials. Experience with oncology medical strategies and clinical trial implementations are required. Leadership experience managing scientific staff is required. Subspecialty training in the area of oncology is highly desired. Experience in the business development area would be a plus. Excellent written and oral communication skills, particularly strong formal presentation skills; strong interpersonal skills commensurate with the need to work closely with outside physicians/ scientists and numerous in-house support groups; knowledge of scientific methods, research design and medical practices and procedures that would be acquired through clinical experience and clinical research studies; good understanding of the current legal and regulatory environment are critical skills in this role. Basic knowledge and appropriate application of biostatistics is required in this role. Must be willing to travel up to 40% with up to 10% international travel.
Daiichi Sankyo, Inc.	Terre Haute	IN	9/9/2010
Sales Representative, Primary Care 2 - Terre Haute, IN
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred
Daiichi Sankyo, Inc.	Seattle	WA	9/9/2010
Hospital Sales Representative - Seattle North, WA
Education and Experience Guidelines: Bachelor’s Degree from an accredited four-year institution required; advanced degree desirable A total of 3 years of pharmaceutical sales experience; Cardiovascular and or Hospital experience preferred Broad healthcare market business acumen and industry knowledge. Outstanding verbal communication skills a must. Ability to self-motivate. Attention to detail. Must possess an executive presence.
Daiichi Sankyo, Inc.	Oklahoma City	OK	9/9/2010
Sales Representative, Primary Care 3 - Oklahoma City North, OK
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred
Daiichi Sankyo, Inc.	Edison	NJ	9/9/2010
Clinical Study Manager
Education/Experience Bachelor’s Degree in Life Sciences or higher. A minimum of 3 years of experience in clinical research (at least 2 of these in Clinical Development) in pharmaceutical or device company, Academic Research Organization or CRO with BS. Minimum of 2 years of clinical research experience with MS, MPH, PhD or higher. Complete understanding of the concepts and applications of clinical research, medical terminology and other disciplines involved in drug development. Proficient skills in computer applications such as Word, Excel, and PowerPoint. Strong oral and written communication skills. Complete knowledge of GCP, FDA CFRs and ICH Guidelines. Ability to interpret data and to present results in a concise and clear manner. Management and leadership skills to contractors to the successful completion of the project. Working knowledge of the components and key content requirements of IND & NDAs.
Daiichi Sankyo, Inc.	Parsippany	NJ	9/9/2010
Senior Analyst Field Analytics
Education/Experience: Qualified candidates will have a Bachelor's Degree; preferably in Business Administration, Quantitative Methods, Market Research, Information Management or a related field. MBA is preferred. Candidates should have 3-5 years of experience, preferably in a Sales Operations function in the pharmaceutical industry, and 3-4 years of experience that should include report development and sales analytics. Must have systems experience with 2 of 4 of the following: decision support, data warehousing, management reporting and sales force automation. Knowledge of Pharmaceutical Syndicated Data (a plus), such as IMS’ DDD, Xponent/Xponent Plantrak and analytical software, SPSS or SAS, Dendrite SFA (a plus) and Business Objects is required. Must have demonstrated analytical skills, excellent customer service, communication, presentation, and interpersonal skills. Must be proficient in the application of personal computers and software, including extensive experience with report writing applications and the Microsoft Office Suite. Must be able to manage multiple projects effectively using multi- disciplinary resources to meet project and timeline demands and experience interacting with outside vendors.
Daiichi Sankyo, Inc.	Edison	NJ	9/9/2010
Clinical Study Manager
Education/Experience Qualified candidates must have Bachelor’s Degree in Life Sciences or higher. A minimum of 3 years of experience in clinical research (at least 2 of these in Clinical Development) in pharmaceutical or device company, Academic Research Organization or CRO with BS. Minimum of 2 years of clinical research experience with MS, MPH, PhD or higher. Complete understanding of the concepts and applications of clinical research, medical terminology and other disciplines involved in drug development. Proficient skills in computer applications such as Word, Excel, and PowerPoint. Strong oral and written communication skills. Complete knowledge of GCP, FDA CFRs and ICH Guidelines. Ability to interpret data and to present results in a concise and clear manner. Management and leadership skills to contractors to the successful completion of the project. Working knowledge of the components and key content requirements of IND & NDAs.
Daiichi Sankyo, Inc.	Pikeville	KY	9/9/2010
Sales Representative, Primary Care 3 - Pikeville, KY
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Sacramento	CA	9/9/2010
Sales Representative, Primary Care 2 - Sacramento West, CA
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Binghamton	AL	9/9/2010
Sales Representative, Primary Care 1 - Binghamton/Elmira, NY
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Topeka	KS	9/9/2010
Sales Representative, Primary Care 1 - Topeka, KS
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Edison	NJ	9/9/2010
CMO Manager
Education/Experience Qualified candidates must have a Master's degree in biology, microbiology, biochemistry, or chemical engineering with a minimum of 5 years experience, or a Bachelor's degree with a minimum of 8 years experience of hands on clinical and/or commercial industry experience in the manufacturing science of biologics (mAbs) and/or cell based therapeutics. Interaction with contract manufacturing organizations and biotech product companies is required and technology transfer and process scale-up are a plus. The skills needed for this position are adequate knowledge of cGMPs, regulatory requirements, and CMC operations in a biotech company; and excellent negotiation and communication skills.
Daiichi Sankyo, Inc.	Edison	NJ	9/9/2010
Manager, Informatics
Education/Experience Qualified candidatees must have a Bachelors Degree in Computer Science, Life science, Engineering, Business Administration and / or a related discipline is required.Masters Degree in Life Science or Engineering or Information systems is preferred. At least 4 years experience in working in pharmaceutical industry clinical research and development with its regulatory constraints, preferably with experience in 21 CFR Part 11; participating in multi-discipline implementation teams to deliver information systems on budget and against aggressive timelines; experience working with senior level scientific and/or professional staff in the Drug Development/Discovery area on the implementation and use of computer-based technologies; working with software and information technology providers; MS Project, PowerPoint, Access, Excel, Word; working knowledge of SDLC; and end-user support. Ability to define, select and implement robust regulatory-compliant information systems solutions to support drug development. Understanding of scientific enterprise and business requirements gathering. Detail-oriented; ability to work independently. Diplomatic and assertive user-facing skills (to manage and meet user expectations). Business and technical problem-solving skills, including root-cause analysis, SWOT, and risk analysis. Strong and persuasive interpersonal skills (to obtain cooperation across multiple functional areas – both internal and external – for on-time and on-budget project implementation). Strong oral and written communication skills. Demonstrated technical skills in computer development environment (e.g., SQL, MySQL, R, S-Plus, SAS, Oracle, Perl, InforSense). PMP certification; Accreditation with a relevant Domain informatics professional body; and Travel to DS locations which will include overnight travel.
Daiichi Sankyo, Inc.	Parsippany	NJ	9/9/2010
Analyst, Regional Market Planning
Education/Experience Requirements: Qualified candidates will have a Bachelor's Degree, preferably in Business, Computer Science or similar field; MBA preferred. Candidates will have at least 2 years experience in market analysis, marketing research or pharmaceutical sales.Two years of experience in pharmaceutical sales is highly desirable. It is essential that you have a demonstrated ability to analyze data in an independent, proactive and creative manner and make actionable recommendations. Proficiency in Business Objects, SPSS, MS Access and Excel is highly desirable. Familiarity with IMS, WK and other data sources is required.
Daiichi Sankyo, Inc.	Parsippany	NJ	9/9/2010
Manager, Area Training Support
Education/Experience: Qualified candidates will have a 4 year college degree; Master's degree in Adult Education, Curriculum/Instruction is preferred. Society of Pharmaceutical and Biotech Trainer membership preferred. Must have the following experience: five plus years overall professional experience; two plus years pharmaceutical sales and at least one year as a Sales Trainer. We are looking for someone with demonstrated superior selling skills expertise. Must possess excellent presentation and facilitation skills, strong interpersonal skills (mentoring and coaching), and problem solving skills.
Daiichi Sankyo, Inc.	Jackson	MS	9/9/2010
Sales Representative, Primary Care 3 - Jackson South, MS
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Gulfport	MS	9/9/2010
Sales Representative, Primary Care 1 - Gulfport, MS
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	San Diego	CA	9/9/2010
Hospital Sales Representative - San Diego, CA
Education and Experience Guidelines: Bachelor’s Degree from an accredited four-year institution required; advanced degree desirable A total of 3 years of pharmaceutical sales experience; Cardiovascular and or Hospital experience preferred Broad healthcare market business acumen and industry knowledge. Outstanding verbal communication skills a must. Ability to self-motivate. Attention to detail. Must possess an executive presence.
Daiichi Sankyo, Inc.	Billings	MT	9/9/2010
Sales Representative, Primary Care 2 - Billings, MT
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred
Daiichi Sankyo, Inc.	Parsippany	NJ	9/9/2010
Exec. Medical Dir Medical Research TA Head - Hypertension & Metabolism
Education/Experience Qualified candidates must have a MD degree with a minimum of 10 years experience in clinical, research or academic medicine and a minimum of 7 years of pharmaceutical industry experience; leadership experience managing scientific staff; and experience with cardiovascular medical strategies and clinical trial implementations. Advanced training in cardiovascular medicine is highly desired. Experience in the business development area would be a plus. Excellent written and oral communication skills, particularly strong formal presentation skills; strong interpersonal skills commensurate with the need to work closely with outside physicians/ scientists and numerous in-house support groups; knowledge of scientific methods, research design and medical practices and procedures that would be acquired through clinical experience and clinical research studies; good understanding of the current legal and regulatory environment are critical skills in this role. Basic knowledge and appropriate application of biostatistics is required in this role. Additional training in the area of cardiovascular medicine is highly desired; experience with hypertension and metabolism products are required Must be willing to travel up to 40% with up to 10% international travel.
Daiichi Sankyo, Inc.	Parsippany	NJ	9/9/2010
Year Round Information Systems Application Intern
Education/Experience Requirements: Qualified candidates will be currently enrolled in an undergraduate program, in at least your junior year of study; Candidates may also be in a graduate program, in an accredited program with a concentration in Information Technology along with business management or related field. Prior experience in a corporate business environment is preferred; experience in an Information Technology Department is a plus. Candidate should be good problem solvers and have understanding of basic algorithms. It is required that you have strong interpersonal, communication and time management skills as well as a proficiency in Microsoft Office (Word, Excel, and Power Point). Knowledge of using some of the following programming languages, software programs, technologies and/or skills is preferred: HTML, DHTML, JAVA, XML, CSS, and Database concepts
Daiichi Sankyo, Inc.	Oklahoma City	OK	9/9/2010
Sales Representative, Primary Care 2 - Oklahoma City North, OK
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Hagerstown	MD	9/9/2010
Sales Representative, Primary Care 1 - Hagerstown, MD
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Washington	DC	9/9/2010
Sales Representative, Primary Care 3 - North Washington, DC
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Westchester	NY	9/9/2010
Hospital Sales Representative, Westchester, NY
Education and Experience Guidelines: Bachelor's Degree from an accredited four-year institution required; advanced degree desirable A total of 3 years of pharmaceutical sales experience; Cardiovascular and or Hospital experience preferred Broad healthcare market business acumen and industry knowledge. Outstanding verbal communication skills a must. Ability to self-motivate. Attention to detail. Must possess an executive presence.
Daiichi Sankyo, Inc.	Lansdale	PA	9/9/2010
Sales Representative, Primary Care 3 - Lansdale, PA
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Kingsport	TN	9/9/2010
Sales Representative, Primary Care 3 - Kingsport, TN
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	New Rochelle	NY	9/9/2010
Sales Representative, Primary Care 2 - New Rochelle, NY
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Huntington	NY	9/9/2010
Specialty Sales Representative - Huntington, NY
Requirements: BS/BA Degree. Two or more years of pharmaceutical sales experience.
Daiichi Sankyo, Inc.	Jacksonville	FL	9/9/2010
Specialty Sales Representative - Jacksonville North, FL
Requirements: BS/BA Degree. Two or more years of pharmaceutical sales experience.
Daiichi Sankyo, Inc.	Edison	NJ	9/9/2010
Staff Biostatistician
Education/Experience Qualified candidates must have Statistics, Biostatistics, or Mathematics: MS or PhD. PhD + 8 yrs or MS + 10 years of pharmaceutical industry experience; full knowledge of advanced statistical analytical methods, clinical trial research, regulatory requirements, coding techniques, and statistical software. Excellent oral and written communication skills; project planning skills; demonstrated experience in analyzing clinical trial data; priority setting skills; multi-tasking skills; problem solving skills; eye for detail; exercise good judgment; and works well within team framework. Comprehensive project management skills. Demonstrated competency in SAS. Regular attendance at IDT Meetings is necessary; experience in managing CROs and external vendors.
Daiichi Sankyo, Inc.	Evanston	IL	9/9/2010
Sales Representative, Primary Care 1 - Evanston, IL
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred
Daiichi Sankyo, Inc.	Las Cruces	NM	9/9/2010
Sales Representative, Primary Care 1 - Las Cruces, NM
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	San Diego	CA	9/9/2010
Sales Representative, Primary Care 3 - San Diego, CA
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Parsippany	NJ	9/9/2010
Senior Auditor
Education/Experience Qualified candidates must have Bachelors degree with 3 or more years auditing experience in GAAP/auditing and accounting principles. Focus in internal controls and fraud prevention is preferred. Knowledge of business processes and internal controls and experience auditing those processes for control weaknesses and reliable financial reporting; and experience conducting interviews of employees/vendors/customers is preferred. Demonstrated abilities and competencies in Sarbanes Oxley and/or J-SOX; COSO Integrated Control Framework; PCAOB Auditing Standards; IIA’s International Standards for the Professional Practice of Internal Auditing; SAS 99; and Generally Accepted Accounting Principles (GAAP) is also required. CPA or CFE and Public Accounting Experience is preferred. Must be willing to travel 15% of the time.
Daiichi Sankyo, Inc.	Parsippany	NJ	9/9/2010
Manager, Training Development
Education/Experience Qualified candidates must have a 4 year college degree with a minimum of 5 years of pharmaceutical industry experience; minimum of 2 years pharmaceutical sales experience and a minimum of 1 year of Sales Training experience. Completion of Level 1 Trainers Certification is required; Project Management and Leadership Development is preferred. Outstanding disease state & product knowledge; excellent presentation & facilitation skills; and proficiency in MS Office Suite are required in this role. Must be willing to travel 30% of the time including field contacts, advisory board and task force meetings, National Meetings, POA meetings and additional training initiatives.
Daiichi Sankyo, Inc.	Newport News	VA	9/9/2010
Sales Representative, Primary Care 3 - Newport News, VA
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Madison	WI	9/9/2010
Sales Representative, Primary Care 3 - Madison, WI
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Fort Lauderdale	FL	9/9/2010
Sales Representative, Primary Care 3 - Fort Lauderdale, FL
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Chico	CA	9/9/2010
Sales Representative, Primary Care 1 - Chico, CA
Requirements: BS/BA Degree. Two or more years of pharmaceutical sales experience.
Daiichi Sankyo, Inc.	Wichita Falls	TX	9/9/2010
Sales Representative, Primary Care 1 - Wichita Falls, TX
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Parsippany	NJ	9/9/2010
Manager, Predictive Modeling
Education/Experience: Qualified candidates must have a Bachelors degree, or an equivalent combination of education and experience in Business, Mathematics, Economics, Statistics or other discipline appropriately focused on analysis and a minimum of 5 years of pharmaceutical industry experience with 1-3 years of experience developing and maintaining forecasts and other predictive models for pharmaceutical products, marketing initiatives, and market events. Experience includes characterizing market dynamics that influence pharmaceutical product performance. High level analytical thinking and problem solving; ability to work cross functionally to incorporate a broad range of perspectives and to provide actionable outputs to all stakeholders up to executive level; advanced proficiency with Microsoft Excel (advanced functions and Visual Basic); and proficiency with presentation software are critical skills in this role. Must be willing to travel 10% of the time.
Daiichi Sankyo, Inc.	Charleston	SC	9/9/2010
Sales Representative, Primary Care 3 - Charleston, SC
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Edison	NJ	9/9/2010
Director, Modeling and Simulation
Education/Experience Qualified candidates must have a Ph.D. in Pharmaceutical science or equivalent. Minimum requirement 8 years clinical pharmacology and pharmacokinetics experience, including implementation of state of art modeling and simulation to support compound development. Expertise in M&S in support of cardiovascular, oncology and diabetics preferred. In-depth knowledge of current regulatory requirements (FDA, GCP and ICH). Ability to work independently and to effectively prioritize, proactively identify and resolve problems and work in a team environment. Must possess excellent communication and interpersonal skills, as well as effective collaboration and negotiation techniques. Highly proficient in standard computer software (Word, Excel and Power Point) and helpful to have proficiency in specialized software for pharmacokinetic data analysis. Demonstrated experience in population pharmacokinetic-pharmacodynamic modeling required using NONMEM. Experience in clinical trials simulation desirable.
Daiichi Sankyo, Inc.	Mobile	AL	9/9/2010
Hospital Sales Representative, Mobile, AL
Education and Experience Guidelines: Bachelor's Degree from an accredited four-year institution required; advanced degree desirable A total of 3 years of pharmaceutical sales experience; Cardiovascular and or Hospital experience preferred Broad healthcare market business acumen and industry knowledge. Outstanding verbal communication skills a must. Ability to self-motivate. Attention to detail. Must possess an executive presence.
Daiichi Sankyo, Inc.	Cleveland	OH	9/9/2010
Sales Representative, Primary Care 1 - Cleveland West, OH
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred
Daiichi Sankyo, Inc.	Parsippany	NJ	9/9/2010
Sr. Manager, Training and Policy
Education/Experience Qualified candidates must have a bachelor's degree and a minimum of 7 years of experience in pharmaceutical sales management, marketing management, training, instructional design, policy development or a combination of the above; ability to establish & maintain credibility and trust throughout the organization; strong writing ability and instructional design and training presentation skills; ability to analyze and synthesize information and to draw conclusions; source and manage vendors are critical skills in this role. Familiarity with pharmaceutical company training requirements; familiarity with OIG and trade association guidance documents, prosecutions and CIAs, Sentencing Guidelines and best practices for corporate compliance programs; FDA and pharma experience; sales, marketing, training and policy development experience are also required in this role. Must be willing to travel 20% of the time.
Daiichi Sankyo, Inc.	Des Moines	IA	9/9/2010
Sales Representative, Primary Care 2 - Des Moines W, IA
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred
Daiichi Sankyo, Inc.	Lufkin	TX	9/9/2010
Sales Representative, Primary Care 2 - Lufkin, TX
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Las Vegas	NV	9/9/2010
Sales Representative, Primary Care 3 - Las Vegas, NV
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Allentown	PA	9/9/2010
Sales Representative, Primary Care 3 - Allentown, PA
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Edison	NJ	9/9/2010
Sr. Director, Clinical Development, Oncology
Education/Experience Qualified candidates must have a MD and a minimum 5 years of pharmaceutical development experience and at least 3 years of hands-on experience managing a major, multi-country, clinical program. Must be an Oncologist. Knowledge of pharmaceutical business, worldwide drug development and regulatory process. Expertise in complex clinical trial design (i.e. factorial design, etc.) and complex implementation (i.e. including Steering Committees, Safety Monitoring Boards, etc.) as well as the interpretation of scientific data. Independent thinking, creativity and innovation. Ability to deliver high quality products. Strong interpersonal skills and ability to interface effectively with multinational development teams in a multicultural working environment. Excellent communication, presentation and negotiation skills with emphasis on building consensus. Ability to effectively manage interactions with academic thought leaders ensuring optimal cooperation for achieving program and department goals. Ability to anticipate and facilitate issue resolution in a multicultural working and business environment.
Daiichi Sankyo, Inc.	Edison	NJ	9/9/2010
Associate Director, Accounting
Education/Experience Qualified candidates must have a Bachelor’s Degree in Business Administration, Finance or Accounting required, MBA and/or CPA preferred. Seven to Ten years experience in financial reporting or financial analysis and accounting combined with strong project management skills. The Finance Department's responsibilities are primarily project related in nature and require employees to demonstrate the following skills; teamwork, initiative, problem solving, creativity, and decision making abilities. Strong financial and accounting skills with equal strength in general business acumen. Strong interpersonal skills to effectively interact and influence people from other functional areas.
Daiichi Sankyo, Inc.	Chesapeake	VA	9/9/2010
Sales Representative, Primary Care 1 - Chesapeake, VA
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Parsippany	NJ	9/9/2010
Coordinator, Organization and Talent Development
Education/Experience Qualified candidates must have a high school degree or equivalent with a minimum of 4 years administrative office experience. Experience in a Human Resources and/or Training environment is strongly preferred. Some college experience is desired. Experience working with internal and external personnel management level is preferred. Excellent organizational and follow up skills; experience working in detailed environment; ability to prioritize and balance numerous priorities and meet deadlines in a challenging fast paced environment are critical skills in this role. Expert level knowledge of MS Office is also required. Experience using training management and newsletter software and SAP is preferred. Must be willing to travel 10% of the time.
Daiichi Sankyo, Inc.	Edison	NJ	9/9/2010
Director, Regulatory Operations
Education/Experience BS or MS degree in Life Sciences is essential. Experience in the pharmaceutical industry with more than 15 years of direct regulatory affairs experience. Working knowledge of laws, regulations and guidelines is essential. Experienced in filing INDs, NDAs in both paper and electronic formats. Experienced in managing an operations group. Basic computer skills (MS Word, Excel and Acrobat) are vital. Knowledge of InSight Publisher and Microsoft Project are a plus. Excellent interpersonal skills are required.
Daiichi Sankyo, Inc.	Parsippany	NJ	9/9/2010
Sr Director Health Economics and Outcomes Research
Education/Experience Qualified candidates must have a Doctoral degree in Health Economics, Health Services Research, Medicine, Public Health, or Pharmacoepidemiology and a minimum of 12 years relevant experience in the healthcare industry with at least 8 years within a pharmaceutical company. Must have atleast 3 years of successful leadership and people management experience (HEOR specific), with five or more years preferred, and track record of effective application of HEOR data with external stakeholders in the United States and International markets clearly tied to successful business outcomes is required. Combination of leadership and hands on experience with HEOR research methodologies during all phases of product life cycle and knowledge of cardiology and oncology disease is preferred. Strong leadership and managerial skills, and ability to successfully influence cross functional teams including senior level clinical and commercial colleagues in order to drive the “value proposition” development agenda are critical skills in this role. Must be willing to travel 20% of time.
Daiichi Sankyo, Inc.	Houston	TX	9/9/2010
Sales Representative, Primary Care 1 - Hosuton, TX Overhire
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Las Cruces	NM	9/9/2010
Sales Representative, Primary Care 3 - Las Cruces, NM
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Baltimore	MD	9/9/2010
Sales Representative, Primary Care 3 - Baltimore West, MD
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Oklahoma City	OK	9/9/2010
District Manager, Primary Care 3 - Oklahoma City, OK
Experience and Education Requirements: Bachelor's Degree required. Minimum 3 years Pharmaceutical sales experience. Previous management experience preferred. OR 4 years Pharmaceutical experience, with a minimum of 2 years sales experience and 2 years of home office experience (e.g. marketing, sales operations, sales training). Overnight travel up to fifty percent required.
Daiichi Sankyo, Inc.	Louisville	KY	9/9/2010
Sales Representative, Primary Care 1 - Louisville South, KY
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Columbus	OH	9/9/2010
District Manager, Primary Care 3 - Columbus, OH
Experience and Education Requirements: Bachelor's Degree required. Minimum 3 years Pharmaceutical sales experience. Previous management experience preferred. OR 4 years Pharmaceutical experience, with a minimum of 2 years sales experience and 2 years of home office experience (e.g. marketing, sales operations, sales training). Overnight travel up to fifty percent required.
Daiichi Sankyo, Inc.	Columbus	OH	9/9/2010
Specialty District Manager, Columbus, OH
Requirements: BS/BA Degree. Two or more years of Primary Care or Specialty District Management experience.
Daiichi Sankyo, Inc.	Monterey	CA	9/9/2010
Sales Representative, Primary Care 3 - Monterey, CA
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Parsippany	NJ	9/9/2010
Director Human Resources Business Partner - Field
Education/Experience Qualified candidates must have a Bachelor’s degree; Master's degree is preferred. Minimum of 10 years of progressive Human Resources experience with at least 3 years supervising HR professionals is required. Experience of the pharmaceutical industry and working with field based functions in highly preferred. You will be accountable for the confidentiality of employee data and required to travel to business area offices on a quarterly basis. Must be willing to travel 15% of the time.
Daiichi Sankyo, Inc.	Parsippany	NJ	9/9/2010
Human Resources Intern
div>Education/Experience Qualified candidates must be currently enrolled in at least their junior year of an accredited undergraduate or graduate program with a concentration in Human Resources or related field. Prior experience in a corporate business environment is preferred; experience in Human Resources Department a plus. It is required that you are proficient with Microsoft Office (Word, Excel, and Power Point). Strong interpersonal skills, communication skills (oral and written), and time management skills are essential.
Daiichi Sankyo, Inc.	Grand Rapids	MI	9/9/2010
District Manager, Primary Care 3 - Grand Rapids, MI
Experience and Education Requirements: Bachelor's Degree required. Minimum 3 years Pharmaceutical sales experience. Previous management experience preferred. OR 4 years Pharmaceutical experience, with a minimum of 2 years sales experience and 2 years of home office experience (e.g. marketing, sales operations, sales training). Overnight travel up to fifty percent required.
Daiichi Sankyo, Inc.	Waterbury	CT	9/9/2010
Sales Representative, Primary Care 1 - Waterbury, CT
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Baltimore	MD	9/9/2010
Hospital Sales Representative, Baltimore NE, MD
Education and Experience Guidelines: Bachelor's Degree from an accredited four-year institution required; advanced degree desirable A total of 3 years of pharmaceutical sales experience; Cardiovascular and or Hospital experience preferred Broad healthcare market business acumen and industry knowledge. Outstanding verbal communication skills a must. Ability to self-motivate. Attention to detail. Must possess an executive presence
Daiichi Sankyo, Inc.	Lafayette	IN	9/9/2010
Sales Representative, Primary Care 3 - Lafayette, IN
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Asheboro	NC	9/9/2010
Sales Representative, Primary Care 2 - Asheboro, NC
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred
Daiichi Sankyo, Inc.	Denver	CO	9/9/2010
District Manager, Primary Care 3 - Denver, CO
Experience and Education Requirements: Bachelor's Degree required. Minimum 3 years Pharmaceutical sales experience. Previous management experience preferred. OR 4 years Pharmaceutical experience, with a minimum of 2 years sales experience and 2 years of home office experience (e.g. marketing, sales operations, sales training). Overnight travel up to fifty percent required.
Daiichi Sankyo, Inc.	Walnut Creek	CA	9/9/2010
Sales Representative, Primary Care 2 - Walnut Creek, CA
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred
Daiichi Sankyo, Inc.	Massapequa	NY	9/9/2010
Sales Representative, Primary Care 3 - Massapequa, NY
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred
Daiichi Sankyo, Inc.	Albuquerque	NM	9/9/2010
Specialty Sales Representative - Albuquerque, NM
Requirements: BS/BA Degree. Two or more years of pharmaceutical sales experience.
Daiichi Sankyo, Inc.	Jacksonville	FL	9/9/2010
Sales Representative, Primary Care 2 - Jacksonville West, FL
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred
Daiichi Sankyo, Inc.	Edison	NJ	9/9/2010
Staff Biostatistician
Education/Experience Qualified candidates must have a MS or PhD in Statistics, Biostatistics, or Mathematics. PhD + 8 yrs or MS + 10 years of pharmaceutical industry experience; full knowledge of advanced statistical analytical methods, clinical trial research, regulatory requirements, coding techniques, and statistical software. Excellent oral and written communication skills; project planning skills; demonstrated experience in analyzing clinical trial data; priority setting skills; multi-tasking skills; problem solving skills; eye for detail; exercise good judgment; and works well within team framework. Comprehensive project management skills.Demonstrated competency in SAS. Regular attendance at IDT Meetings is necessary; experience in managing CROs and external vendors. Must be willing to travel 10% of the time.
Daiichi Sankyo, Inc.	Parsippany	NJ	9/9/2010
Lead Applications Administrator, CP&A
Education/Experience Qualified candidates must have a bachelors degree or commensurate experience and a minimum of 5 years IT experience, 2 years of experience developing and supporting web applications using Oracle, Java, Java web services, Java EJB, XML; 2 years using Oracle, SQL, PL/SQL and 2 years with application configuration, upgrades, rollout and support experience. Experience in the pharmaceutical industry, managed markets contracting, with exposure to Commercial, Medicaid, Medicare, GPO and other federal markets and with I-Many CLM and Revenue Management Suite is highly preferred. Knowledge of pharmaceutical industry pricing, contracting practices and key contract management processes (Rebates and Admin Fees, Membership) is highly preferred. Good SQL and analytical skills and the ability to evaluate user requirements and capability to design and develop solutions to meet those requirements are important in this role. Oracle SQL, PL/SQL, Web Development, DHTML, Java EJB, J2EE/Java, Java Webservices, XML and JBoss are required skills; BI Tools are a plus in this role.
Daiichi Sankyo, Inc.	Saint Paul	MN	9/9/2010
Sales Representative, Primary Care 3 - Saint Paul, MN
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Syracuse	NY	9/9/2010
Sales Representative, Primary Care 2 - Syracuse, NY
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Fredericksburg	VA	9/9/2010
Sales Representative, Primary Care 3 - Fredericksburg, VA
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Edison	NJ	9/9/2010
Manager, Medical Writing
Education/Experience Qualified candidates must have a PharmD, PhD in biological sciences. MD is strongly preferred. Otherwise exceptional candidates with a MS or BS/BA may be considered. Minimum requirement of 3 years experience with PharmD or PhD, 5 years with Masters’ Degree or 7 years with a BA/BS. Experience in writing regulatory documents (protocols, Investigator Brochures [IBs], Clinical Study Reports (CSRs), clinical sections of the CTD [2.5, 2.7.3, 2.7.4], integrated summaries of efficacy and safety [ISE and ISS], briefing books, and regulatory responses) in the pharmaceutical or CRO environment required; ability to interpret and organize scientific data; and general understanding of clinical research, biostatistics, electronic publishing, and relevant industry guidelines (GCP, eCTD, and ICH). Marketing submission experience (NDAs or MAAs) preferred but not required. Daiichi Sankyo develops or has developed drugs in the following therapeutic areas: cardiovascular diseases, metabolic diseases, inflammation and immunology, infectious diseases, and oncology. Relevant therapeutic area experience preferred. Ability to quickly get up to speed on a therapeutic area, project, or indication with little to no coaching, work concurrently on several complex projects, meet aggressive deadlines, and adjust priorities rapidly as the situation demands. Strong interpersonal and communication skills (both verbal and written) are also required as the individual must be able to work in a team environment and coordinate with the team to move documents forward to completion. Must be a self-motivated person who can work with limited guidance/supervision. Excellent writing skills with a clear concise style and excellent grammar, punctuation, and spelling; proficiency in a Microsoft Windows environment; and strong MS Word skills and ability to work with templates. Excellent attention to details, especially as related to accuracy of numbers/statements and consistency within and across documents.
Daiichi Sankyo, Inc.	Santa Monica	CA	9/9/2010
Sales Representative, Primary Care 3 - Santa Monica, CA
Education and Experience Requirements: BS/BA. Pharmaceutical sales experience with a background in cardiovascular medication preferred.
Daiichi Sankyo, Inc.	Fort Myers	FL	9/9/2010
Hospital Sales Representative - Fort Myers, FL
Education and Experience Guidelines: Bachelor’s Degree from an accredited four-year institution required; advanced degree desirable A total of 3 years of pharmaceutical sales experience; Cardiovascular and or Hospital experience preferred Broad healthcare market business acumen and industry knowledge. Outstanding verbal communication skills a must. Ability to self-motivate. Attention to detail. Must possess an executive presence.
Daiichi Sankyo, Inc.	Houston	TX	9/9/2010
Sales Representative, Primary Care 2 - Houston Central, TX
Requirements: BS/BA Degree. Two or more years of pharmaceutical sales experience.
GE Healthcare	na	CA	9/9/2010
Product Specialist ? Filtration and Single-Use
* This is a home office based sales position and as such the candidate must reside within their territory in order to support this role. * Bachelor?s degree in chemical engineering or mechanical engineering. * 3+ years of hands-on experience with BioProcess filtration and/or fluid-handling technologies * Excellent oral presentation and technical writing skills. * Overnight travel, up to 50%, is required. To the extent that you are applying for a position that requires you to operate a GE owned/leased, privately owned/leased or rental vehicle for company business, you must have a valid drivers license and be willing to submit to a check of your driving records. GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics * Working knowledge of UNICORN * Hands-on experience in process development for sizing and optimizing filtration processes * Strong background in the use of single-use products for normal-flow filtration, cross-flow filtration and fluid handling. * Technical sales or sales support experience or direct employment in a biotech or pharmaceutical production or process development environment. * This position requires a high degree of self-motivation and prioritization skills. The candidate must also have a talent for getting along with and working productively with a variety of highly motivated sales personalities.
GE Healthcare	na	MD	9/9/2010
Field Service Engineer
* Bachelor?s degree, Electrical Engineering, Electrical Engineering Technology, equivalent military education or Associates Degree with 2 years experience servicing electronic equipment, or a High School Diploma/GED and 12 or more years experience servicing electronic equipment. * Experience interfacing with both internal team members and external customers as part of a solution based service process. * Experience diagnosing and repairing mechanical, electromechanical, and/or electronic equipment. * Experience troubleshooting and responding to customer concerns. GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics Excellent analytical and communication skills with the ability to communicate complex technical issues in an easy to understand manner * Six Sigma trained/certified * Change agent and process oriented.
GE Healthcare	Piscataway	NJ	9/9/2010
Global Marketing Director - Cell Therapy Devices
* MBA or Master?s degree in Marketing, Business Administration or comparable experience * Undergraduate degree in a life sciences or medical field of study * 8+ years experience in product marketing or product management of medical devices for regenerative medicine, or related field * 3 or more years experience in a leadership role with direct reports and budget responsibility * Must be able to work flexibly and travel up to 50% of time (25% overseas) GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics * Experience in regulatory affairs around and/or manufacturing of medical devices and/or cell therapy * 5+ years Product development expertise, including: NPI process, product roadmap development, product life-cycle management * Demonstrated project management skills * Excellent oral and written communications skills * Proven ability to network and influence to engage customers in an early dialogue * Proven ability to grasp complex scientific and medical concepts * Leadership skills to lead teams and shape/lead growth vision and marketing strategy * Innovation ? develop new ideas through collaboration and execute on creative ideas * Negotiation skills to work collaboratively with existing customers and engage in discussions with new external parties * Experience working within a global matrix environment * Documented analytical skills to clearly develop, evaluate, and present options and business cases
GE Healthcare	Westborough	MA	9/9/2010
Project Leader, Black Belt
Education/Knowledge: * Degree in Mechanical engineering, plastics engineering, or a related field * BS with a min of 10 years relevant industry experience or MS with a min. of 6 years of relevant industry experience * Strong analytical and quantitative statistical skills; facility with Six Sigma concepts and tools * Working understanding of regulatory issues related to Biopharmaceutical manufacturing and licensure related to medical devices Skills: * Negotiation, communication, presentation and listening skills * Fluency in written and spoken English Standard Microsoft Office packages and statistical software Basic project management Experience: Work in a regulated environment (e.g., GMP or ISO quality system) Other: Authorization to work in the USA Ability to travel domestically and internationally on an occasional basis Ability to perform physical tasks that require mobility, manual dexterity, and visual acuity GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics * Change agent with strong credibility and influence in the organization * Masters degree in business related field * Demonstrated ability to motivate others and achieve results * Demonstrated commitment for process improvement and product quality * Customer-focused in defining quality and establishing priorities Strong oral and written communication skills Strong interpersonal and leadership skills Executive level presentation skills
GE Healthcare	Piscataway	NJ	9/9/2010
Scientist II-HC
Bachelor?s degree in Biology, Chemistry, Engineering or related Life Science discipline - 5+ years bioprocess experience in a (bio)chemical laboratory in an industrial setting - Willingness to travel up to 25-50% - Prior experience interacting with Customers - Demonstrated ability to troubleshoot bioprocesses GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics - Master's degree in Biology, Chemistry, Engineering or related Life Science discipline - Strong industrial experience in purification of biomolecules (upstream, downstream, technology transfer, validation, process development, biomanufacturing) - Working experience in industrial biopharmaceutical purification - Experience with chromatography techniques: IEX; HIC; AC; RPC; IMAC and SEC - Experience with filtration methods- Experience in Disposable biomanufacturing - Strong Background in the purification of biomolecules - Experience in working in cGMP environment - Working knowledge of FDA/EMEA regulations for biologics (Phase I-III manufacture) - Proven skills working in a global team with global Customers
GE Healthcare	na	MD	9/9/2010
Planner/Scheduler
* At least two years of experience in an administrative support or coordinator role * High School Diploma * Demonstrated computer skills, including Microsoft Outlook, Word & Excel GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics * MS Access or other database experience * Understanding of the Life Sciences Industry and service delivery * Experience negotiating with Original Equipment Manufacturers and Vendors * Inventory management experience * Effective written and verbal communication skills * Ability to Work independently with minimum direction * Must be willing to walk and climb stairs as necessary * Must be willing to enter laboratory work environments as needed * Ability to work in a matrix environment * Strong Interpersonal Skills * Knowledge of a parts ordering System * Fluent in English Language * Ability to identify problems and support action plans for problem resolution
GE Healthcare	Northampton	MA	9/9/2010
Quality Control Manager
1. Bachelor?s degree (or high school diploma/GED plus 4 years of related work experience) * At least 3 years of experience working in one of the following areas: regulated medical device, regulated pharmaceutical environment, quality control/assurance, or regulatory assurance * At least 1 year of management experience to include direct reports * Ability to effectively communicate using English (or local language) GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics * Demonstrated managerial experience * Bachelors of Science in a related discipline (electronics, mechanics, thermodynamics, biochemistry) * Leadership and motivational skills * Organizational skills * Fine attention to Detail
GE Healthcare	na	WA	9/9/2010
Account Manager - Life Sciences Capital Equipment
* You must be willing to work out of a home office and able to service the NW US territory. (Washington and Oregon) * Bachelor?s degree in a scientific field. * 3 or more years of experience in Life Sciences in the areas of Protein Detection and analysis with special focus on imaging and scanning. * 3 or more years of commercial sales OR capitol equipment experience * Computer Literacy: Microsoft and Outlook * Overnight travel is required. * To the extent that you are applying for a position that requires you to operate a GE owned/leased, privately owned/leased or rental vehicle for company business, you must be willing to submit to a check of your driving records. GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics * BS degree in Biology, Chemistry, Biochemistry, or Chemical Engineering * MBA * Willing to work out of a home office in Seattle WA. * 2 or more years laboratory experience or clinical experience. * Sales Experience with biotechnology/pharmaceutical industries in Life Sciences research. * Sales Training Experience: Commercial Selling Skills Training. * Proven effective sales record in previous positions. * Direct employment in biotech or pharmaceutical research, production or process development environment.
GE Healthcare	Piscataway	NJ	9/9/2010
Americas EHS Leader (Life Sciences)
* Bachelor of Science in Environmental, Civil, or Chemical Engineering, Hydrogeology or Geology or related technical discipline * 5 years experience managing environmental site characterization investigations (Phase I, II, etc), remedial investigation, feasibility study, remedial design, risk assessment, remediation, demolition, decontamination, etc. * Regulatory knowledge and experience working under U.S. federal and state and /or equivalents regulations covering contamination, site investigation and property transfer such as CERCLA, RCRA, OSHA, TSCA, ISRA, etc. and capable of learning requirements and applying this experience internationally * Compliance experience with federal and state EHS regulations (CAA, CWA, OSHA, codes, etc) * Proven project and program management skills GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics * Experience working with GE products or within any GE business * Advanced degree (MS) and/or professional certifications (PG, PE, LSP, etc) * Experience managing projects and/or EHS compliance in Europe or Asia and familiarity with European and Asian environmental laws * Able to simultaneously manage multiple projects and other responsibilities, adjust to changing priorities and to make decisions with speed and accuracy based on available information * Team player with strong interpersonal skills, capable of working within a globally diverse, cross-functional, internal and external team across different time zones * Excellent oral and written communication, presentation, and negotiation skills
GE Healthcare	na	NJ	9/9/2010
Account Manager , Research Sciences
* BS degree in Biology, Chemistry, Biochemistry, or Chemical Engineering and/or BS/BA with relevant experience in Life Sciences. * Minimum of 3 years successful commercial experience performance that exceeded plan: Including but not limited to sales, marketing, technical support, field applications support. * Sales Training Experience: Commercial Selling Skills Training. * Computer Literacy: Microsoft and Outlook * Good interpersonal and communication skills, plus experience of using these skills to participate in cross-functional teams. * Fluency and effective speaking skills in relevant local language. * Self-Motivated, a team player and well organized. * Overnight travel is required. * This is a home office based sales position and as such the candidate must reside within 50 miles of the specified territory in order to support this role. * To the extent that you are applying for a position that requires you to operate a GE owned/leased, privately owned/leased or rental vehicle for company business, you must be willing to submit to a check of your driving records. You must be willing to submit to a background investigation, including for example, verification of your past employment, criminal history and educational background. * You must be willing to take a drug test. * You must be willing to work out of a home office based in the specified territory. GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics * MBA * Practical chromatography/imaging/filtration lab experience. * Sales Experience with biotechnology/pharmaceutical industries in Life Sciences research. * Strong presentation skills. * Proven effective sales record in previous positions. * Direct employment in biotech
GE Healthcare	na	CA	9/9/2010
Regional Sales Director - West Region
* A minimum of 5 successful years selling ion the life sciences market * Demonstrated success in sales strategy development and implementation * A bachelors degree GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics * Excellent communication, presentation, and interpersonal relation skills * Demonstrated negotiation skills * Strong sales data analysis skills * Proven ability to manage a budget * Goal focused leader capable of building a strong teamwork environment
GE Healthcare	na	CA	9/9/2010
Sales Representative 1-HC
* Bachelor of Science Degree in a Life Science/Sciences * 2 or more years sales experience within a Life Sciences or Medical Device industry GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics * Experience with distributor sales * Experience working in and managing client in a laboratory environment
GE Healthcare	Piscataway	NJ	9/9/2010
Key Accounts & Team Manager
- BA/BS degree in Business or Technical Discipline. - At least 5 years of leadership experience in corporate world or military - At least 5 years experience in a Customer Service or Call Center Environment - At least 2 years managing key or strategic accounts - Direct customer relationship experience - Demonstrated leadership experience through managing, supervising or training team members GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics - MBA - Proven leadership and ability to orchestrate resources and motivate teams. - Strong business acumen. - Ability to develop and execute multiple priorities and approaches to meet objectives - Exceptional interpersonal skills - An inclusive leader that builds a connection to the workforce through personal involvement and trust - Proven ability to influence and drive change through exceptional written and verbal communication skills - Demonstrated tendency to challenge the status quo and drive constant improvement in process and ability to achieve organizational goals - Understanding of customer/marketplace and drivers that influence customer behavior - Previous direct report management/leadership experience - Ability to resolve complex issues within functional area and/or area of expertise - Ability to develop and execute multiple priorities and approaches to meet objectives
GE Healthcare	Piscataway	NJ	9/9/2010
Modality Leader - Research Sciences
* BS Degree in a Life Science discipline such as Biology, Microbiology, Chemistry, Biochemistry, Genetics, Molecular Biology, Chemical Engineering * A minimum of 7 years of life sciences sales management experience, key account management, sales management, marketing , scientific support and/or training * Demonstrated basic computer skills in Microsoft Word, Excel, PowerPoint, Outlook or equivalent Overnight travel is required GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics * MBA * Masters or PhD. in Scientific field * Relevant sales management experience preferred (8+ years) * Experience working in a laboratory setting * Willingness and ability to take on additional responsibilities and undertake challenging tasks and/or global projects * Proven ability to interact and influence cross functionally at all levels internally and externally * This position requires a high degree of self-motivation. * The candidate must possess a sense of what is most important and needs to be done next, while maintaining a ?customer first? attitude * Ability to prioritize activities to ensure customer satisfaction and at the same time maximize profits is required * Talent for getting along with and working productively with a variety of highly motivated sales personalities * Experience and ability to develop and implement the global strategy and structure in line with business strategy * Time management, organizational, and administrative skills * Relevant experience in a life science marketing role * Advanced degree in Life Science related curriculum and business administration. * Ability to consolidate and communicate insights in an actionable way to facilitate growth; understand rationale of management requirements and translate into key takeaways * Excellent communication skills and ability to interface with senior management. * Proactive, self-starter that will both execute and identify opportunities to add value/insights to the leadership team and make process improvements to drive efficiencies. * Ability to multi-task in a dynamic growth-oriented environment
GE Healthcare	na	MD	9/9/2010
On-Site Engineer
* Associates Degree with at least 2 years experience servicing electronic equipment, or equivalent military education or a High School Diploma/GED and 5+ years experience servicing electronic equipment. * Must have experience servicing major OEM Life Science equipment. * Willingness to take a drug test * Must have a valid driver's license The applicant must submit to GEHC's standard background check at the time of hire and must be legally authorized to work in the United States. This position may, in the future, support GEHC contracts with the U.S. government. In doing so, the successful candidate must submit to and clear a governmental background check. GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics * Service experience with any of the following systems: HPLC, GC, LCMS, Mass Spectrometers, Liquid Handlers, PCRs, Plate Washers/Readers or Flow Cytometers * Bachelor degree in electronics, computer science, or life sciences is desirable. * Extensive computer and software knowledge. * Proven successful customer service experience. * Proven professionalism and leadership qualities. * Strong written and verbal communication skills.
GE Healthcare	na	MD	9/9/2010
Site Director -Scientific Asset Service Program
* Bachelors degree in Electrical Engineering, Electronic Technology or related technical field; OR Associates Degree in Electronics and 3 years experience servicing electronic equipment in the field * Previous management of direct reports, leadership, or supervisory experience * Strong computer competency with solid understanding of Microsoft operating systems (Windows 2000, Windows XP) and Microsoft Office. * Must be able to lift at least 40 pounds This position is open to candidates within GE. GE will only employ those who are legally authorized to work in the United States for this role. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics * Bachelor of Science Electrical Engineering Technology with college level courses in Biochemistry/Biology * Ability to drive organizational change and process improvement * At least 3 years experience with direct report or leadership responsibilities * Familiarity with GLP/GMP requirements and/or IQ/OQ. * Proven ability to develop and execute multiple priorities and approaches to meet objectives and experience in matrix organization * Field service background and knowledge of Life Sciences market and instruments * Working knowledge of asset management program * Excellent communication skills, both written and verbal * Ability to engage and motivate teams * Strong verbal and written communication skills
GE Healthcare	na	CA	9/9/2010
Product Specialist, Cell Culture
* This is a home office based sales position and as such the candidate must reside within their territory in order to support this role * Bachelor?s degree in chemical engineering, mechanical engineering, biochemical engineering or biology * 3+ years field sales or applications or technical support of single-use BioProcess products, OR * 3+ years of hands-on experience using single-use cell culture and fluid-handling technologies * Excellent oral presentation and technical writing skills * Overnight travel, up to 50%, is required.To the extent that you are applying for a position that requires you to operate a GE owned/leased, privately owned/leased or rental vehicle for company business, you must have a valid drivers license and be willing to submit to a check of your driving records. GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics * Knowledge of WAVE product portfolio. * Strong background in cell culture and the use of single-use products and fluid handling. * Filtration experience a plus * Technical sales or sales support experience or direct employment in a biotech or pharmaceutical production or process development environment * Proven effective sales record in previous positions. * This position requires a high degree of self-motivation and prioritization skills. * The candidate must also have a talent for getting along with and working productively with a variety of highly motivated sales personalities.
GE Healthcare	Piscataway	NJ	9/9/2010
Inventory Leader
1. Bachelors Degree with 5 years related experience in warehousing, distribution, inventory management * Proficient in Microsoft Office products * Manufacturing experience helpful * Candidate identified GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics 1. Strong interpersonal and communication skills * Ability to identify and drive cost saving intiatives
GE Healthcare	na	CA	9/9/2010
Account Manager - Forensics & Human Identity
* Bachelor of Science Degree in a Life Science/Sciences * 2 or more years sales experience within a Life Sciences or Medical Device industry. GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics * Demonstrated experience within the Forensic/Human Identity Market * Experience working with DNA testing products * Candidate must reside within specified territory (Western US)
BD (Becton, Dickinson and Company)	San Antonio	TX	9/9/2010
Associate Care Specialist (12 Open Positions)
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Consolidations Team Leader
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BD (Becton, Dickinson and Company)	San Antonio	TX	9/9/2010
HR Analyst/Specialist, Continuous Improvement
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BD (Becton, Dickinson and Company)	San Antonio	TX	9/9/2010
HR Analyst/Specialist, Learning Administration
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BD (Becton, Dickinson and Company)	San Antonio	TX	9/9/2010
HR Analyst/Specialist, Leave Administration
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BD (Becton, Dickinson and Company)	San Antonio	TX	9/9/2010
HR Analyst/Specialist, Payroll Administration
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BD (Becton, Dickinson and Company)	San Antonio	TX	9/9/2010
HR Analyst/Specialist, Reporting and Analytics
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BD (Becton, Dickinson and Company)	San Antonio	TX	9/9/2010
HR Partner ? North America Shared Service Center
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BD (Becton, Dickinson and Company)	San Antonio	TX	9/9/2010
HR Specialist/Analyst, Employee Data Management (EDM)
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BD (Becton, Dickinson and Company)	San Antonio	TX	9/9/2010
HR Specialist/Analyst, Global Mobility
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BD (Becton, Dickinson and Company)	San Antonio	TX	9/9/2010
HR Specialist/Analyst, Performance Management and HR Planning Administration
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BD (Becton, Dickinson and Company)	San Antonio	TX	9/9/2010
HR Specialist/Analyst, Talent Acquisition Administration
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BD (Becton, Dickinson and Company)	San Antonio	TX	9/9/2010
Manager, North American Associate Service Center
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Regulatory Affairs Specialist
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BD (Becton, Dickinson and Company)	San Antonio	TX	9/9/2010
Team Leader, Associate Care
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BD (Becton, Dickinson and Company)	San Antonio	TX	9/9/2010
Team Leader, Specialist/Analysts
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Administrative Assistant
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BD (Becton, Dickinson and Company)	San Antonio	TX	9/9/2010
Administrative Assistant
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Administrative Assistant
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Analyst
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Applications Programmer (.NET)
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BD (Becton, Dickinson and Company)	San Jose	CA	9/9/2010
Assembly Technician I, Repair Center
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Associate Medical Director
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BD (Becton, Dickinson and Company)	Sandy	UT	9/9/2010
Associate Medical Director, Medical Affairs
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Associate Medical Director, Medical Affairs
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BD (Becton, Dickinson and Company)	Baltimore	MD	9/9/2010
Associate Scientist
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BD (Becton, Dickinson and Company)	Sandy	UT	9/9/2010
Back-up Mechanic
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
BDM PS US Purchasing Manager
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BD (Becton, Dickinson and Company)	San Diego	CA	9/9/2010
Biochemist I - BDB
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BD (Becton, Dickinson and Company)	Research Triangle Park	NC	9/9/2010
Biological Scientist
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BD (Becton, Dickinson and Company)	Baltimore	MD	9/9/2010
Bioreactor Scientist
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BD (Becton, Dickinson and Company)	Baltimore	MD	9/9/2010
Buyer/Planner
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BD (Becton, Dickinson and Company)	Billerica	MA	9/9/2010
Channel Manager
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Channel Protection Manager - Forensic Accounting
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BD (Becton, Dickinson and Company)	San Jose	CA	9/9/2010
Clinical Data Manager
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Clinical Laboratory Specialist
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BD (Becton, Dickinson and Company)	Baltimore	MD	9/9/2010
Clinical Principal Statistician
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Clinical Trial Associate I
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BD (Becton, Dickinson and Company)	San Jose	CA	9/9/2010
Commodity Specialist - Team Lead
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BD (Becton, Dickinson and Company)	Sumter	SC	9/9/2010
Cost and Budget Supervisor
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BD (Becton, Dickinson and Company)	San Jose	CA	9/9/2010
CRM Data Administrator
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BD (Becton, Dickinson and Company)	San Diego	CA	9/9/2010
Custom Applications Scientist
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BD (Becton, Dickinson and Company)	San Jose	CA	9/9/2010
Data Base Administrator II
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Director of Global Health Policy and Practice
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BD (Becton, Dickinson and Company)	Billerica	MA	9/9/2010
Director of Manufacturing - Process Development
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Director of Marketing, Prefilled Initiative
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BD (Becton, Dickinson and Company)	Billerica	MA	9/9/2010
Director Quality Engineering
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BD (Becton, Dickinson and Company)	Billerica	MA	9/9/2010
Director R&D - Electrical and Software Engineering
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BD (Becton, Dickinson and Company)	Billerica	MA	9/9/2010
Director R&D - Program Manager
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BD (Becton, Dickinson and Company)	Billerica	MA	9/9/2010
Director R&D - Systems Engineering
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Director, R&D, WW Self Administration of Injectable Systems
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BD (Becton, Dickinson and Company)	Holdrege	NE	9/9/2010
Electrical Controls Technician I B/D Shift
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BD (Becton, Dickinson and Company)	Canaan	CT	9/9/2010
Electrical Engineer
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BD (Becton, Dickinson and Company)	Columbus West	NE	9/9/2010
Environmental Engineer - 1st Shift
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BD (Becton, Dickinson and Company)	San Jose	CA	9/9/2010
Facilities Maintenance Technician III Electrician
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BD (Becton, Dickinson and Company)	Columbus East	NE	9/9/2010
Finals Inspector 2nd shift
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BD (Becton, Dickinson and Company)	Columbus East	NE	9/9/2010
Finals Inspector 3rd Shift
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BD (Becton, Dickinson and Company)	Columbus West	NE	9/9/2010
Financial Coordinator
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Global IT Service Planner
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Global Security Analyst
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Global Telephony Engineering Lead
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BD (Becton, Dickinson and Company)	Columbus West	NE	9/9/2010
IECO Setup, Instuct & Repair 2nd Shift
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BD (Becton, Dickinson and Company)	Columbus West	NE	9/9/2010
Injection Molding Technician B Shift
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BD (Becton, Dickinson and Company)	San Jose	CA	9/9/2010
Instrument Assembly Associate II
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BD (Becton, Dickinson and Company)	San Jose	CA	9/9/2010
Instrument Assembly Associate III
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BD (Becton, Dickinson and Company)	San Francisco	CA	9/9/2010
Instrument Specialist
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BD (Becton, Dickinson and Company)	San Jose	CA	9/9/2010
Instrument Test Associate I
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BD (Becton, Dickinson and Company)	San Diego	CA	9/9/2010
Inventory Control Coordinator
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
IP Docketing Clerk
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
IP Specialist
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
IT Compliance Specialist
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BD (Becton, Dickinson and Company)	Columbus West	NE	9/9/2010
IT Programmer / Business Analyst - 1st shift
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
IT Validation Engineer
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
IT Validation Engineer
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
IT Validation Engineer
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BD (Becton, Dickinson and Company)	Sumter	SC	9/9/2010
Lead Technical Associate
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BD (Becton, Dickinson and Company)	Columbus East	NE	9/9/2010
Luer Production Lead - B Shift (Time in Job bidding restrictions lifted for CC 1305)
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BD (Becton, Dickinson and Company)	San Jose	CA	9/9/2010
Manager Clinical Research Associates
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Manager International Taxes & Audits
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BD (Becton, Dickinson and Company)	Teterboro	NJ	9/9/2010
Manager of Flight Operations
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BD (Becton, Dickinson and Company)	Billerica	MA	9/9/2010
Manager R&D - Mechanical Engineering and Design
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BD (Becton, Dickinson and Company)	Billerica	MA	9/9/2010
Manager R&D - Software Development
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BD (Becton, Dickinson and Company)	San Jose	CA	9/9/2010
Manager Software Engineering
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Manager, Corporate Safety and Industrial Hygiene
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BD (Becton, Dickinson and Company)	Sandy	UT	9/9/2010
Manager, R&D
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Manager, R&D
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BD (Becton, Dickinson and Company)	Woburn	MA	9/9/2010
Manufacturing Associate 1
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BD (Becton, Dickinson and Company)	Wilson	NC	9/9/2010
Manufacturing Associate I
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BD (Becton, Dickinson and Company)	Wilson	NC	9/9/2010
Manufacturing Associate II
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Manufacturing Director - Plastics/SAIS
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BD (Becton, Dickinson and Company)	Canaan	CT	9/9/2010
Manufacturing Engineer
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BD (Becton, Dickinson and Company)	Burlington	NC	9/9/2010
Manufacturing Technician I, Reagents
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BD (Becton, Dickinson and Company)	Burlington	NC	9/9/2010
Manufacturing Technician I, Reagents
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BD (Becton, Dickinson and Company)	Billerica	MA	9/9/2010
Marketing Communications Manager
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BD (Becton, Dickinson and Company)	Wilson	NC	9/9/2010
Master Data Coordinator
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BD (Becton, Dickinson and Company)	San Jose	CA	9/9/2010
Material Controller II
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BD (Becton, Dickinson and Company)	Baltimore	MD	9/9/2010
Material Handler III
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BD (Becton, Dickinson and Company)	Baltimore	MD	9/9/2010
Material Handler III
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BD (Becton, Dickinson and Company)	Baltimore	MD	9/9/2010
Material Handler III
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BD (Becton, Dickinson and Company)	Baltimore	MD	9/9/2010
Material Handler III
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Medical Specialist
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BD (Becton, Dickinson and Company)	Columbus East	NE	9/9/2010
Microbiology Laboratory Coordinator
See above
BD (Becton, Dickinson and Company)	Holdrege	NE	9/9/2010
Molding Process Engineer
See above
BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Molding Technology Engineer
See above
BD (Becton, Dickinson and Company)	Columbus West	NE	9/9/2010
Needle Products Associate 3rd Shift
See above
BD (Becton, Dickinson and Company)	Columbus West	NE	9/9/2010
Needle Products Setup Operator 2nd Shift
See above
BD (Becton, Dickinson and Company)	Columbus West	NE	9/9/2010
Needles Coordinator - 3rd shift
See above
BD (Becton, Dickinson and Company)	Canaan	CT	9/9/2010
Packaging Engineer
See above
BD (Becton, Dickinson and Company)	San Diego	CA	9/9/2010
Packaging Technician I
See above
BD (Becton, Dickinson and Company)	Baltimore	MD	9/9/2010
Phone Support Engineer
See above
BD (Becton, Dickinson and Company)	Baltimore	MD	9/9/2010
Pilot Lab Operator III
See above
BD (Becton, Dickinson and Company)	Sumter	SC	9/9/2010
Plastics Molding Engineer - Injection Molding
See above
BD (Becton, Dickinson and Company)	Columbus West	NE	9/9/2010
Plastipak Set Up Operator - 2nd shift (Grade 7 certifies to Grade 8)
See above
BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Principal Engineer
See above
BD (Becton, Dickinson and Company)	Billerica	MA	9/9/2010
Principal Engineer
See above
BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Principal Engineer
See above
BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Principal Engineer
See above
BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Principal Engineer
See above
BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Principal Engineer
See above
BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Principal Engineer Technical Lead
See above
BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Principal Engineer, Mechanical/Environmental
See above
BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Principal Engineer- Pen Injection Platform
See above
BD (Becton, Dickinson and Company)	Sandy	UT	9/9/2010
Principal Polymer Engineer
See above
BD (Becton, Dickinson and Company)	Columbus West	NE	9/9/2010
Process and Automation Development Engineer-PosiFlush
See above
BD (Becton, Dickinson and Company)	Sandy	UT	9/9/2010
Process Technician
See above
BD (Becton, Dickinson and Company)	Sandy	UT	9/9/2010
Process Technician
See above
BD (Becton, Dickinson and Company)	Madison	WI	9/9/2010
Process Technician
See above
BD (Becton, Dickinson and Company)	Baltimore	MD	9/9/2010
Product Manager
See above
BD (Becton, Dickinson and Company)	Billerica	MA	9/9/2010
Product Manager - Cell Culture Environment
See above
BD (Becton, Dickinson and Company)	Baltimore	MD	9/9/2010
Product Manager - Software
See above
BD (Becton, Dickinson and Company)	Columbus East	NE	9/9/2010
Production Coach B Shift
See above
BD (Becton, Dickinson and Company)	Baltimore	MD	9/9/2010
Production Operator II
See above
BD (Becton, Dickinson and Company)	Baltimore	MD	9/9/2010
Production Operator III
See above
BD (Becton, Dickinson and Company)	Baltimore	MD	9/9/2010
Production Operator III
See above
BD (Becton, Dickinson and Company)	Baltimore	MD	9/9/2010
Production Operator IV
See above
BD (Becton, Dickinson and Company)	San Diego	CA	9/9/2010
Production Planner II
See above
BD (Becton, Dickinson and Company)	Broken Bow	NE	9/9/2010
Production Shift Facilitator - 12 hr shift - Blue Nights
See above
BD (Becton, Dickinson and Company)	Broken Bow	NE	9/9/2010
Project Engineer
See above
BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	9/9/2010
Project Engineer R&D
See above
BD (Becton, Dickinson and Company)	San Jose	CA	9/9/2010
Project Manager/System Engineer
See above
BD (Becton, Dickinson and Company)	Miami	FL	9/9/2010
Project Scientist
See above
BD (Becton, Dickinson and Company)	Baltimore	MD	9/9/2010
Project Statistician
See above
BD (Becton, Dickinson and Company)	San Diego	CA	9/9/2010
QC Associate I - BDB
See above
BD (Becton, Dickinson and Company)	Baltimore	MD	9/9/2010
QM Engineer
See above
BD (Becton, Dickinson and Company)	Wilson	NC	9/9/2010
Quality Assurance Associate
See above
BD (Becton, Dickinson and Company)	Wilson	NC	9/9/2010
Quality Assurance Specialist
See above
BD (Becton, Dickinson and Company)	Wilson	NC	9/9/2010
Quality Assurance Specialist
See above
BD (Becton, Dickinson and Company)	Wilson	NC	9/9/2010
Quality Control Chemist Technician
See above
BD (Becton, Dickinson and Company)	Wilson	NC	9/9/2010
Quality Control Microbiology Technician
See above
BD (Becton, Dickinson and Company)	Baltimore	MD	9/9/2010
Quality Management Principal Engineer - Instruments
See above
BD (Becton, Dickinson and Company)	San Jose	CA	9/9/2010
Repair Technician II