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Company Jobs - AstraZeneca Pharmaceuticals



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Kathy @ AstraZeneca Pharmaceuticals

   


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Architect: Innovation Project Leader/2 Year fixed-term/Cambridge/Luton

Luton Bedfordshire

Relevant expertise and experience: - The ability to travel both domestically and internationally - Technical, Scientific or Business degree --- Master's degree preferred - Experience of Program Management methodologies with delivery in agile environments - Excellent communication, relationship management, and influencing skills - Proven track record negotiating & influencing across complex groups - Experience shaping innovative solutions - Experience working in global organization and across cultural boundaries - Coaching, facilitation & consultation skills

Posted On - 10/22/2014 7:18:50 AM

Labeling Associate Director

Macclesfield Cheshire

Key Relationships to reach solutions Internal and External Contacts/Customers: * GRLs/XRADs/RPMs * Patient Safety * Clinical * Regulatory personnel at the Marketing Companies * Operations * Commercial Education, Qualifications, Skills and Experience Minimum requirements: * University Degree in Science or related discipline * 3 to 5 years pharmaceutical experience, including regulatory experience, preferably working with labeling * Knowledge of labeling regulations and guidances * Excellent verbal and written communication skills * Keen attention to detail and accuracy * Multi-cultural awareness and sensitivity; demonstrated experience effectively communicating and negotiating in diverse cultures. * Ability to assimilate clinical and scientific information and present it in a concise manner * Ability to think strategically, appropriately assess risks and formulate strategies to manage risk * Must demonstrate competencies in: * Building Relationships (works well across formal and informal networks) * Negotiation Skills (good listener; able to build a consensus) * Critical Information Seeking (works well across formal and informal networks) * Rational Persuasion (able to distil an issue to its key components and suggest solutions) * Interpersonal Awareness (aware of how actions affect other people) Preferred Background: * Experience in Labeling development and/or maintenance * Knowledge of major markets Labeling regulations * Advanced academic training is highly desirable (PharmD, PhD) Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation

Posted On - 10/22/2014 7:18:50 AM

Labeling Manager

Macclesfield Cheshire

Key Relationships to reach solutions Internal and External Contacts/Customers: * GRLs/XRADs/RPMs * Patient Safety * Clinical * Regulatory personnel at the Marketing Companies * Operations * Commercial Education, Qualifications, Skills and Experience Minimum requirements: * University Degree in Science or related discipline * 3 years pharmaceutical experience, preferably regulatory experience, preferably working with labeling * Knowledge of labeling regulations and guidances * Excellent verbal and written communication skills * Keen attention to detail and accuracy * Multi-cultural awareness and sensitivity; demonstrated experience effectively communicating and negotiating in diverse cultures. * Ability to assimilate clinical and scientific information and present it in a concise manner * Ability to think strategically, appropriately assess risks and formulate strategies to manage risk * Must demonstrate competencies in: * Building Relationships (works well across formal and informal networks) * Negotiation Skills (good listener; able to build a consensus) * Critical Information Seeking (works well across formal and informal networks) * Rational Persuasion (able to distil an issue to its key components and suggest solutions) * Interpersonal Awareness (aware of how actions affect other people) Preferred Background: * Experience in Labeling development and/or maintenance * Knowledge of major markets Labeling regulations * Advanced academic training is highly desirable (PharmD, PhD) Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation

Posted On - 10/22/2014 7:18:50 AM

Study Delivery Coordinator 12 Month Contract

Mississauga Ontario

Finance * Review, assess, approve and process payments associated with Clinical Study Agreements, ensuring accordance with the terms of the agreement and financial guidelines * Set up and maintaining the payment terms within the appropriate systems. * Review, analyze and resolving payment discrepancies and queries * Collation and execution of regular clinical cheque runs. Study Drug & Non- Drug Supplies * Manage non drug supplies, by developing, inputting into, sourcing, ordering, initiating the shipment, tracking, reviewing stock level, and approving materials for destruction * Provide drug label approvals. * Coordinate or execute import shipping approvals * Prepare and execute Statement of Work (SOW) with vendor for local drug management * Mange, coordinate and oversee the activities of the local drug management vendor ensuring accordance with the SOW. * Collaborate with Global Investigational Product Supplies units to ensure seamless delivery of clinical drug supplies * Collaborate and communicate with global study teams and local regulatory contacts, to assess Canadian requirements for comparator and/or rescue medication, and source from local providers if required * Review, discuss, and communicate packaging and labelling requirements, as defined by the protocol, with vendors * Responsible for the notification, investigation and resolution of product quality complaints For Investigator Sponsored Studies / Fellowships / Funding Agreements: * Track and update recruitment in order to assess variance between planned and actual timelines for the study * Assess, review, report and manage financial variances between actual and planned spend across the budget. * Prepare, execute, track, collect, review and assess * Execute, track, collect, review and assess the documentation, required as per regulatory guidelines. * Manage (set-up / update / close) associated systems. * Manage (source / budget / procure) study supplies and investigational product Unspecified * University degree in Health Science, or a related field (an equivalent combination of education, training, and work experience may be considered) * Two years experience in Clinical Research or related industry * Understanding of Good Clinical Practices/International Committee on Harmonization principles * Strong interpersonal and communication skills (written and oral). Especially need to be comfortable with speaking to Health Care Professionals. * Ability to influence without authority * Able to work effectively both independently and in a team environment. * Self-motivated and able to display autonomy and initiative ? for instance; able to take action, move actions forward and make decisions without the need for continual supervision or consultation. * Strong attention to detail * Ability to manage multiple demands/projects simultaneously * Effective time management skills * Solid Customer Service orientation * Good knowledge of MS Office (Word, Excel, PowerPoint) * Comfortable with technology and using multiple computer systems * French speaking considered an asset. Interviews: Only candidates who meet the minimum requirements as outlined above, will be interviewed. Internal candidates who are interested in this position must inform their manager before they apply.

Posted On - 10/22/2014 7:18:50 AM

Supervisors

Macclesfield Cheshire

Minimum Requirements - Education and Experience Essential: * Experience of FDA/cGMP or other regulated quality system. * Proven supervisory experience within manufacturing or support. * Understanding and application of Lean manufacturing principles. * Effectively problem solve. Desirable: * Degree (or similar) in a Science discipline. * Knowledge and application of Safety, Health and Environment principles. * Experience in formulation, filling or packaging. * Experience of sterile/aseptic operations. AstraZeneca welcomes applications from all sections of the community. An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex or national origin, and will not be discriminated against on the basis of disability.

Posted On - 10/22/2014 7:18:50 AM

Senior Counsel-Data Privacy

Cambridge Cambridgeshire

All AZ global legal counsel are expected to develop their legal and leadership capabilities, including the flexibility and the ability to support legal work outside their core area of legal expertise. - Law degree. - Professional legal qualification. - Relevant legal practice experience. - Good interpersonal and communication skills. - Proven skills in analyzing and solving issues related to data privacy. Legal Experience requirements The Senior Counsel will be expected to have strong expertise in the following legal areas: - Data privacy laws and practice globally, and in the UK. - Data privacy elements of commercial contracts. - Freedom of Information legislation. - European Convention on Human Rights. - Clinical Trials Directive (preferred but not essential). - Pharmacovigilence legislation (preferred but not essential).

Posted On - 10/22/2014 7:18:50 AM

Architect: Innovation Project Leader/2 Year fixed-term/Cambridge/Luton

Cambridge Cambridgeshire

Relevant expertise and experience: - The ability to travel both domestically and internationally - Technical, Scientific or Business degree --- Master's degree preferred - Experience of Program Management methodologies with delivery in agile environments - Excellent communication, relationship management, and influencing skills - Proven track record negotiating & influencing across complex groups - Experience shaping innovative solutions - Experience working in global organization and across cultural boundaries - Coaching, facilitation & consultation skills

Posted On - 10/22/2014 7:18:49 AM

Diabetes Sales Specialist - DOV2 - Warner Robins, GA

Warner Robins GA

Qualifications: Education: -Bachelors degree (any major) from an accredited college or university is required. Experience: - Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required - Demonstrated effective organizational and communication skills - Leadership, self--motivation and initiative - Demonstrated judgment and decision-making capability - Be results oriented with demonstrated time management skills - Ability to learn, analyze, understand and convey complex information - Demonstrated technical aptitude and computer skills are essential - A valid driver's license and safe driving record Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation LocationGA, Warner Robins CategorySales Date Posted10/20/2014 Req Number14-50090330 NoticeAstraZeneca does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on AstraZeneca's approved agency list. Unsolicited resumes or candidate information submitted to AstraZeneca by search/recruiting agencies not already on AstraZeneca's approved agency list, and who were not asked to work on a specific vacancy, shall become the property of AstraZeneca and if the candidate is subsequently hired by AstraZeneca, AstraZeneca shall not owe any fee to the submitting agency. AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialisation of prescription medicines, primarily for the treatment of cardiovascular, metabolic, respiratory, inflammation, autoimmune, oncology, infection and neuroscience diseases. AstraZeneca operates in over 100 countries and its innovative medicines are used by millions of patients worldwide. For more information please visit www.astrazeneca.com. AstraZeneca Making a Difference AstraZeneca is an equal opportunity employer

Posted On - 10/21/2014 7:33:56 AM

Supervisor, Manufacturing-Packaging

West Chester OH

: Physical Demands Ability to lift 40 pounds, stand for long periods of time, work gowned up for long periods of time, maintain good personal hygiene. Manual Dexterity Unimpaired Manual Dexterity Audible/Visual Demands Correctable vision equal to or better than 20/20. Environment Manufacturing - Works under conditions with minor hazards such as working with moving machinery and equipment. Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation LocationOH, West Chester CategoryManufacturing and Production Date Posted10/20/2014 Req Number14-50114197 NoticeAstraZeneca does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on AstraZeneca's approved agency list. Unsolicited resumes or candidate information submitted to AstraZeneca by search/recruiting agencies not already on AstraZeneca's approved agency list, and who were not asked to work on a specific vacancy, shall become the property of AstraZeneca and if the candidate is subsequently hired by AstraZeneca, AstraZeneca shall not owe any fee to the submitting agency. AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialisation of prescription medicines, primarily for the treatment of cardiovascular, metabolic, respiratory, inflammation, autoimmune, oncology, infection and neuroscience diseases. AstraZeneca operates in over 100 countries and its innovative medicines are used by millions of patients worldwide. For more information please visit www.astrazeneca.com. AstraZeneca Making a Difference AstraZeneca is an equal opportunity employer

Posted On - 10/21/2014 7:33:56 AM

Diabetes Sales Specialist - D3 - Falls Creek, PA

Falls Creek PA

Qualifications: Education: -Bachelors degree (any major) from an accredited college or university is required. Experience: - Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required - Demonstrated effective organizational and communication skills - Leadership, self--motivation and initiative - Demonstrated judgment and decision-making capability - Be results oriented with demonstrated time management skills - Ability to learn, analyze, understand and convey complex information - Demonstrated technical aptitude and computer skills are essential - A valid driver's license and safe driving record Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation LocationPA, Falls Creek CategorySales Date Posted10/20/2014 Req Number14-50101089-1 NoticeAstraZeneca does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on AstraZeneca's approved agency list. Unsolicited resumes or candidate information submitted to AstraZeneca by search/recruiting agencies not already on AstraZeneca's approved agency list, and who were not asked to work on a specific vacancy, shall become the property of AstraZeneca and if the candidate is subsequently hired by AstraZeneca, AstraZeneca shall not owe any fee to the submitting agency. AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialisation of prescription medicines, primarily for the treatment of cardiovascular, metabolic, respiratory, inflammation, autoimmune, oncology, infection and neuroscience diseases. AstraZeneca operates in over 100 countries and its innovative medicines are used by millions of patients worldwide. For more information please visit www.astrazeneca.com. AstraZeneca Making a Difference AstraZeneca is an equal opportunity employer

Posted On - 10/21/2014 7:33:56 AM

Diabetes Sales Specialist - D2 - Charlotte S, NC

Charlotte NC

Qualifications: Education: -Bachelors degree (any major) from an accredited college or university is required. Experience: - Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required - Demonstrated effective organizational and communication skills - Leadership, self--motivation and initiative - Demonstrated judgment and decision-making capability - Be results oriented with demonstrated time management skills - Ability to learn, analyze, understand and convey complex information - Demonstrated technical aptitude and computer skills are essential - A valid driver's license and safe driving record Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation LocationNC, Charlotte CategorySales Date Posted10/20/2014 Req Number14-50090145 NoticeAstraZeneca does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on AstraZeneca's approved agency list. Unsolicited resumes or candidate information submitted to AstraZeneca by search/recruiting agencies not already on AstraZeneca's approved agency list, and who were not asked to work on a specific vacancy, shall become the property of AstraZeneca and if the candidate is subsequently hired by AstraZeneca, AstraZeneca shall not owe any fee to the submitting agency. AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialisation of prescription medicines, primarily for the treatment of cardiovascular, metabolic, respiratory, inflammation, autoimmune, oncology, infection and neuroscience diseases. AstraZeneca operates in over 100 countries and its innovative medicines are used by millions of patients worldwide. For more information please visit www.astrazeneca.com. AstraZeneca Making a Difference AstraZeneca is an equal opportunity employer

Posted On - 10/21/2014 7:33:56 AM

Compliance Project Manager/Senior Manager

Gaithersburg MD

Minimum Specific Requirements: Bachelor's degree (ideally Accounting, Finance) Demonstrated experience in finance, auditing, quality assurance/control, SOX and/or risk management Demonstrated project leadership, strong project management skills with the ability to handle competing projects simultaneously Strong ethical, collaborative and influencing skills Excellent computer skills, including data and reporting software programs Preferred Background: Additional certifications (e.g., CPA, MBA or CIA) Experience in or with the biopharmaceutical industry or a consulting firm working with pharmaceutical clients Knowledge of the Research and Development process Working knowledge of / experience with the US Federal Sunshine and EFPIA requirements Understanding of Global payment transparency Demonstrated knowledge of SAP, and purchase to pay systems / processes, Procurement Global / cross-cultural experience Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation LocationMD, Gaithersburg CategoryOperations Date Posted10/20/2014 Req Number14-50086035 NoticeAstraZeneca does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on AstraZeneca's approved agency list. Unsolicited resumes or candidate information submitted to AstraZeneca by search/recruiting agencies not already on AstraZeneca's approved agency list, and who were not asked to work on a specific vacancy, shall become the property of AstraZeneca and if the candidate is subsequently hired by AstraZeneca, AstraZeneca shall not owe any fee to the submitting agency. AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialisation of prescription medicines, primarily for the treatment of cardiovascular, metabolic, respiratory, inflammation, autoimmune, oncology, infection and neuroscience diseases. AstraZeneca operates in over 100 countries and its innovative medicines are used by millions of patients worldwide. For more information please visit www.astrazeneca.com. AstraZeneca Making a Difference AstraZeneca is an equal opportunity employer

Posted On - 10/21/2014 7:33:56 AM

Cardiology Clinical Research Physician - CVMD Global Medicines Development

Gaithersburg MD

Requirements -- Education and Experience * Graduate of a recognized school of medicine with an M.D. degree or equivalent. * Specialty training and board certification in Cardiology * Clinical experience and strong academic track record in Diabetes * Experience in designing, monitoring and implementing clinical trials and interpreting trial results, including an understanding of biostatistics and safety reporting * Demonstrated leadership qualities, capable of conducting a large study as part of a global team * Functions within a matrix environment, contributes to decision-making and reaching alignment in order to meet challenging timelines * Works collaboratively, respects other working cultures, including Alliance and Academic partners * Good presentation skills. Can communicate effectively with internal stakeholders as well as external partners and collaborators * 5 or more years of Drug Development experience obtained while working in the pharmaceutical industry and/or substantial clinical trial experience collaborating with pharmaceutical sponsors * An understanding of pharmaceutical industry R&D, particularly of major clinical milestones and of the factors which influence those decision points * An understanding of the interplay between clinical development, LCM, commercial objectives and regulatory requirements Organizational Behavior 1. Commitment to Customers and Integrity: Understands one's customers and uses that insight to provide value 2. Strategic Leadership: Quickly identifies and acts on opportunities, combining forethought with action. This is based on an understanding of the external environment and its impact on AZ 3. Acts Decisively: Makes and acts on decisions quickly and effectively and fosters the same in others. This is based on an underlying courage to enable risk-taking for the business 4. Drives Accountability: Holds self and others accountable for the achievement of performance expectations. Creates an environment that enables others to perform at their best 5. Works Collaboratively: Actively creates and promotes cross-boundary collaboration with the aim of achieving better business results. Boundaries can exist between individuals, geographies, cultures, teams, functions, organizations 6. Develops People and Organization: Demonstrates a genuine commitment to the time and effort needed to develop oneself and others Customers: Works with internal and external customers, including Clinical Project Teams, Global Product Teams, Therapy Areas, Global Marketing and Business Development, AstraZeneca Regulatory, External Alliance Partners, Regulatory Authorities (e.g EMA, FDA), and Payer Boards to accomplish tasks related to clinical product development and achievement of market access ensuring satisfaction of these customers. Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation LocationMD, Gaithersburg CategoryResearch and Non-Clinical Development Date Posted10/15/2014 Req Number14-50114964 NoticeAstraZeneca does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on AstraZeneca's approved agency list. Unsolicited resumes or candidate information submitted to AstraZeneca by search/recruiting agencies not already on AstraZeneca's approved agency list, and who were not asked to work on a specific vacancy, shall become the property of AstraZeneca and if the candidate is subsequently hired by AstraZeneca, AstraZeneca shall not owe any fee to the submitting agency. AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialisation of prescription medicines, primarily for the treatment of cardiovascular, metabolic, respiratory, inflammation, autoimmune, oncology, infection and neuroscience diseases. AstraZeneca operates in over 100 countries and its innovative medicines are used by millions of patients worldwide. For more information please visit www.astrazeneca.com. AstraZeneca Making a Difference AstraZeneca is an equal opportunity employer

Posted On - 10/21/2014 7:33:56 AM

Diabetes Sales Specialist - DOV2 - St. Paul, MN

St Paul N MN

Qualifications: Education: -Bachelors degree (any major) from an accredited college or university is required. Experience: - Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required - Demonstrated effective organizational and communication skills - Leadership, self--motivation and initiative - Demonstrated judgment and decision-making capability - Be results oriented with demonstrated time management skills - Ability to learn, analyze, understand and convey complex information - Demonstrated technical aptitude and computer skills are essential - A valid driver's license and safe driving record Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation LocationMN, St Paul N CategorySales Date Posted10/6/2014 Req Number14-50090385 NoticeAstraZeneca does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on AstraZeneca's approved agency list. Unsolicited resumes or candidate information submitted to AstraZeneca by search/recruiting agencies not already on AstraZeneca's approved agency list, and who were not asked to work on a specific vacancy, shall become the property of AstraZeneca and if the candidate is subsequently hired by AstraZeneca, AstraZeneca shall not owe any fee to the submitting agency. AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialisation of prescription medicines, primarily for the treatment of cardiovascular, metabolic, respiratory, inflammation, autoimmune, oncology, infection and neuroscience diseases. AstraZeneca operates in over 100 countries and its innovative medicines are used by millions of patients worldwide. For more information please visit www.astrazeneca.com. AstraZeneca Making a Difference AstraZeneca is an equal opportunity employer

Posted On - 10/21/2014 7:33:56 AM

Associate Principal Scientist Trace Analysis

Macclesfield Cheshire

The successful candidate will be expected to: · Provide scientific leadership in control and analysis of trace impurities · Provide specialist training, development and technical support to drug projects. · Drive excellence in control and analysis of trace impurities in drug product and drug substance. · Provide strategic frameworks, expertise and understanding for Extractables & Leachables, Devices & Packaging, Metal Residues and Potential Mutagenic Impurities analysis and other related areas. · Lead complex projects at any stage of development that have significant risk with respect to control and analysis of trace impurities. · Identify, develop and implement innovative science and technology activities to improve trace analysis capability within AstraZeneca · Develop external contacts (industrial and academic) to drive capability forward. · Present and publish work internally and externally to AstraZeneca. · Manage technical interactions with CROs and external experts. · Influence regulatory framework and guidance for control and analysis of trace impurities. · A degree and/or PhD in Chemistry/Analytical Science · Significant experience of pharmaceutical development with a track record of delivery and creativity and a focus on the application of advanced analytical techniques. · A broad range of expertise in analytical techniques and method development for the analysis of trace impurities. · Ideally you will have experience of at least two phases of pharmaceutical development · An understanding of the regulatory framework for the control and analysis of trace impurities · Experience of leading project work, technical supervision and coaching. · Scientific credibility with a track record of external presentation and publication of notable technical achievements

Posted On - 10/21/2014 7:33:56 AM

Associate Principal Scientist In Vitro Product Performance

Macclesfield Cheshire

Influence regulatory framework and guidance in the area of product performance and understanding · A degree and/or PhD in Chemistry/Analytical Science/Pharmaceutical Science/Pharmacy · Significant experience of pharmaceutical development with a track record of delivery and creativity in the area of product performance and understanding · A broad range of expertise in analytical techniques and method development relevant to the area of product performance and understanding. · Experience of at least two phases of pharmaceutical development · An understanding of the regulatory framework relevant to the area of product performance and understanding. · Experience of leading project work, technical supervision and coaching. · Scientific credibility with a track record of external presentation and publication of notable technical achievements

Posted On - 10/21/2014 7:33:56 AM

Regulatory Affairs Associate Director

Gaithersburg MD

Minimum Requirements --Education and Experience University Degree in Science or related discipline Five year experience of working in one or more areas in regulatory affairs in the pharmaceutical or related industry, or experience at a health authority Leadership skills, including proven leadership of cross-functional project teams experience Excellent written and verbal communication skills Thorough knowledge of the drug development process Thorough scientific knowledge sufficient to understand all aspects of regulatory issues Preferred Experience Knowledge of AZ Business and processes Skills and Capabilities (see attachment for details) Strategic thinking Influencing Problem solving Flexibility/ Adaptability Independence Delivery & Results Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation LocationMD, Gaithersburg CategoryRegulatory Affairs Date Posted7/11/2014 Req Number14-10051650 Special NotesMultiple Positions NoticeAstraZeneca does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on AstraZeneca's approved agency list. Unsolicited resumes or candidate information submitted to AstraZeneca by search/recruiting agencies not already on AstraZeneca's approved agency list, and who were not asked to work on a specific vacancy, shall become the property of AstraZeneca and if the candidate is subsequently hired by AstraZeneca, AstraZeneca shall not owe any fee to the submitting agency. AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialisation of prescription medicines, primarily for the treatment of cardiovascular, metabolic, respiratory, inflammation, autoimmune, oncology, infection and neuroscience diseases. AstraZeneca operates in over 100 countries and its innovative medicines are used by millions of patients worldwide. For more information please visit www.astrazeneca.com. AstraZeneca Making a Difference AstraZeneca is an equal opportunity employer

Posted On - 10/20/2014 7:21:33 AM

Process Leader

Macclesfield Cheshire

Essential: * Degree in a Science discipline. * Experience of FDA/cGMP or other regulated quality system. * Proven line management experience within manufacturing or support. * Understanding and application of Lean manufacturing principles. * Effectively problem solve. * Experienced within a unionised environment. Desirable: * Can coach and embed Lean Manufacturing Principles. * Knowledge and application of SHE principles. * Experience in formulation, filling, packaging, validation, technology transfer or change control. * Experience of sterile/aseptic operations. The role is within a performance driven environment and requires an ability to effectively prioritise across diverse and competing customer needs to maintain team motivation and output whilst under pressure. The environment is highly regulated with compliance and a right first time attitude being underpinning requirements to delivering high performance. AstraZeneca welcomes applications from all sections of the community. An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex or national origin and will not be discriminated against on the basis of disability.

Posted On - 10/20/2014 7:21:33 AM

Associate Project Manager - Secondment / Fixed Term Contract (11mths)

Alderley Park Cheshire

* Degree or equivalent experience in a relevant subject * Working knowledge of Prince II or other Project management training * Specialist level Excel, Microsoft Project, Spotfire and PowerPoint. * Highly organized and structured * Demonstrate skills in project management understanding * Highly developed collaborative skills; able to work with different function and cultures * Interest in and enthusiasm for companion diagnostic development * Proven ability to learn new information effectively * Ability to handle multiple projects; flexibly manage and adapt priorities

Posted On - 10/20/2014 7:21:33 AM

Biotransformation Scientist

Cambridge Cambridgeshire

- Degree in Chemistry/Biochemistry with 5 years directly relevant industrial experience or 3 years experience and a higher degree in a research area directly linked to analytical science. - Extensive experience of structural elucidation of small molecules through the generation and interpretation of high resolution mass spectra, ideally with a focus on metabolite identification and experience of using radiolabeled compounds. - A strong understanding of how metabolite identification studies are carried out in drug development e.g. MIST and hADME studies, how to work with in-vitro colleagues to optimise results and what it takes to provide a regulatory met-id package in the most efficient way is essential. - Significant experience of influencing drug development strategies for Biotransformation studies and generating regulatory documents to feed into project submissions. - Can-do attitude with the ability to work independently to Good Laboratory Standards (GLS), HTA and Radiochemical compliance with minimal direction from line or project leaders. - Track record of successful problem solving, high quality science and influencing of stakeholders, particularly in a drug project context. - Good understanding of the drug discovery process and how DMPK studies contribute to that process. - Desire to carry out scientific development and research work with a view to publishing collaboratively. - Proven ability to work with Thermo scientific FT orbitrap mass spectrometers such as the LTQ- orbitrap XL, Q-Exactive or Orbitrap fusion would be advantageous as would experience of at least one of the following elements: o hADME study delivery and/or dosimetry calculations. o Use of laboratory automation platforms. o Regulatory reporting and GLP. o Line and/or capability management. - Can-do attitude and a desire to learn and adapt is essential. - Strong customer focus with the ability to have robust discussions with project leaders to ensure that project, scientific and resource demands are aligned. - Depending on the skills and experience of the candidate this role may be offered at the Senior or Associate Principle Scientist levels. Deadline for applications - 15th of October 2014 - Laboratory based role split across Cambridge and Alderley Park until 2017. - No line reports. - Part of a group of 13 and sub-team of 3 - Depending on their skills and experience the successful candidate may be able to take on significant leadership of the global Oncology Biotransformation capability. - Opportunities to supervise and coach modern apprentices and sandwich students.

Posted On - 10/20/2014 7:21:33 AM

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