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| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
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| Sr Scientific Associate, Analytical Development |
| - A Master's or Bachelor's degree in the life sciences or physical sciences with a preference for a concentration in Chemistry, Analytical Chemistry or Pharmaceutical Chemistry
- 0 - 4 years of academic experience in a chemistry or analytical chemistry laboratory setting with some previous related industry experience preferred
- Familiarity with, or a desire to gain a working understanding of, HPLC, LC-MS, GC, GC-MS, FT-IR, UV-VIS, KF and other instruments used in the analysis of pharmaceutical products
- An interest in and passion for establishing a career in analytical development and the biopharmaceutical industries
- The ability to work successfully in both a team environment as well as independently
- Excellent written and verbal communication skills
- Established organizational skills
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
 AstraZeneca Pharmaceuticals |
Boston |
MA |
11/19/2009
|
| Intern - Site Services and Logistics |
Currently pursuing a four-year Bachelor degree in Architectural Engineering, Interior Design or Facilities Planning and Management. Would also consider Architecture, Construction Management or Civil Engineering majors. · Courses: Computer Aided Design, Technical drawing, Building Design and Construction · PC proficiency: AutoCAD, MS Office, MS Outlook Skills and Competencies: · Above average to excellent computer skills in AutoCAD, MS Office, MS Outlook; · Ability to read and understand architectural building floor plans, blueprints and construction documents; · Organized work environment skills and good understanding of documentation requirements; · Strong attention to detail; · Demonstrated analytical and troubleshooting skills, excellent safe work habits; · Strong oral and written communication skills; · Ability to follow procedures as dictated by SOP (standards of operation); · General working knowledge of laboratory or commercial building systems.
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| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
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| Sr. Staff Veterinarian |
| Minimum Requirements
?DVM (or equivalent) and licensed to practice in the US or equivalent
?License to practice in at least one state in the United States
?ACLAM board certification or board eligibility
?1 to 5 years of laboratory animal medicine experience, with record of increased responsibilities and accomplishments, in either a pharmaceutical or academic environment
?Knowledge of regulatory requirements for the care and use of animals in research
?Experience working in a matrixed multidisciplinary environment and knowledge of the drug discovery and development process
?Effective communication, organizational and technical skills
?Strong interpersonal skills with an ability to collaborate and work in teams
?Ability to motivate others, positively influence people, and work in a team environment
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| Novartis Oncology |
na |
MA |
11/20/2009
|
| BS/MS Research Associate: Oncology Cell Biologist |
| BS/MS in the sciences with a minimum 5 years of post school experiences preferred. A successful candidate will have demonstrated a high level of competency in hands-on laboratory skills in cell biology, including cell culture, westerns, biochemical enzyme assays, cell based assays including ELISA, RT-PCR, DNA cloning, RNA handling, imaging of cells using microscopes, flow cytometry and various proliferation assays. Must have proficient computer skills in Excel and powerpoint and also should be able to write laboratory reports independently. Candidates from highly reputable biological sciences laboratories in an academic environment as well as those with previous experience in pharmaceutical industry will be considered. |
| Novartis Oncology |
na |
CA |
11/20/2009
|
| Manufacturing Manager (2nd shift)_SF Bay Area |
| Minimum Qualification Requirements:
? A minimum of a Bachelors degree in a scientific discipline is required. Equivalent experience may be accepted.
? A minimum of 8 years experience in GMP pharmaceutical manufacturing industry is required.
? A minimum of 5 years previous management experience preferably in a GMP manufacturing operation is required.
? Strong mechanical aptitude and hands on skills with tools and equipment are required.
? Familiarity with electronic test equipment and control systems is desired.
? Strong verbal and written communication skills are required.
? Must be goal-oriented, quality-conscientious, and customer-focused.
? Good laboratory compliance and safety practices are a must.
? Project management skills are preferred.
? GMP/ISO experience is required.
? Cleanroom experience may be required. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Fellow, Endocrine and Reproductive Toxicology (Cambridge) |
| Minimum Requirements
? Ph.D. degree in Biochemistry, Physiology, Cell Biology, Toxicology or a related Biological Science.
? At least 2 years of prior experience in pharmaceutical drug development and/or toxicological sciences is required
? A strong expertise in hormonal disruption and toxicology, and reprotoxicology
? Experience of managing highly skilled technical staff, laboratory equipment, consumables and safety is desirable.
? Fluency in English (written and spoken) is a must.
? Flexibility and ability to work in a team, comfortable with multitasking, good written and oral communication skills, independent and accurate working style, ability to plan and organise effectively, willingness to take on additional responsibilities are expected. |
| AstraZeneca Pharmaceuticals |
Boston |
MA |
11/19/2009
|
| Translational Strategist - Infection Research |
| Degree level required and minimum years experience:
· A strong candidate would typically have a Ph.D. or M.D./Ph.D. and 10 or more years of experience, or equivalent experience, of which a minimum of 6 years should be in the pharmaceutical industry or other relevant setting
· Experience in anti-bacterial discovery and development is desirable
Competencies (knowledge and skills):
· Internally and externally recognized expertise in a scientific, technical or organizational area and the capacity to apply literature and theoretical concepts to the advancement of Infection portfolio goals.
· Possess strong problem solving skills and the ability to, on the basis of their own experience and analytical skills, ascertain the value of and initiate the use of new techniques for solving problems within and beyond their immediate project.
· Have a complete understanding of the AstraZeneca drug discovery and development process.
· Understand and work towards the AstraZeneca business objectives.
· Be highly productive: consistently generating high quality results within established time frames, even in areas of limited precedent.
· Possess strong knowledge and understanding of relevant database and scientific support software.
· Be a proactive communicator with excellent verbal and written communication and listening skills. Solicit opinions and feedback from others. Deliver presentations that are well thought out, informative and convincing. Able to present work at internal and external meetings when appropriate.
· Able to direct scientific staff and manage their performance.
· Able to effectively negotiate, persuade and influence others in a matrix environment.
· Capable of proposing and implementing scientific, technical or organizational ideas and initiatives.
· Able to manage multiple tasks efficiently, consistently generating high quality results within established time frames, even in areas of limited precedent.
Behaviors:
· Fosters environment of scientific excellence, innovation, productivity and timeliness, leading by example. Is reliable, has strong work ethic, and shows respect for colleagues
· Demonstrates leadership.
· Mentors and provides development opportunities for matrix or direct reports.
· Demonstrates commitment to team goals and consistently demonstrates influence in team & project meetings, advising project teams with respect to technical solutions and potential new approaches for consideration. Seeks solutions to issues that affect team morale and effectiveness
· Proactively shares expertise and ideas and is viewed as a resource by colleagues. Actively seeks to give advice and encouragement to the scientific community, promoting self as an approachable resource.
· Expands personal skills and knowledge as required to be effective. Demonstrates flexibility, open-mindedness, and adaptability. Projects creditability and professionalism. Is candid and honest in discussions
· Act in accordance with all AstraZeneca policies on personnel, SHE, best laboratory practice, etc.
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| Astellas Pharma, Inc. |
Deerfield |
IL |
11/19/2009
|
| Medical Director, Medical Science - Oncology |
| M.D. degree, Board Certified or Board Eligible in Designated SpecialtyMinimum three years clinical experienceMinimum two years laboratory or clinical research experience and five years experience in the pharmaceutical industry or equivalent academic experience.Strong working-knowledge of regulatory procedures and guidelines (preferably US)Effective team player in a matrixed R&D environmentAble to work independently on all aspects of assigned projectsExcellent presentation and writing skillsExcellent organizational skills |
| Johnson & Johnson Family of Companies |
South San Francisco |
CA |
11/19/2009
|
| Director, Medical Writing - Janssen AI, LLC |
| A minimum of a Bachelor's degree in a science or communication discipline with a minimum of 10 years medical writing experience in the clinical or laboratory setting, OR an Advanced Degree with 7 years medical writing experience in a clinical or laboratory setting preferred. Excellent leadership and management experience. Good understanding of experimental methods, research design, and statistical analysis. Ability to analyze medical data and interpret its significance within a pharmaceutical setting. Ability to interpret, analyze, and present statistical data obtained in a clinical trial. Advanced scientific, technical reading, writing and editing skills. Excellent oral communication skills. Proficient computer and word processing skills. Use of templates and experience with document management systems. Up to 5% yearly travel may be required (International as well as Domestic). If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Novartis Oncology |
na |
MA |
11/20/2009
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| Sr Safety Assessment Expert |
| PhD in pharmacology, toxicology or a related biological science; MD with appropriate experience, DVM with appropriate training and experience. PharmD or equivalent with a strong biological background or equivalent work experience.
Languages: Fluent English (oral and written).
Experience/Professional requirement:
1. Level-dependent.
o Base level: At least 2 years experience as a part-time safety assessment project team representative alongside other duties such as study director; experience with biologicals safety assessment desirable.
o Senior level: At least 3 years experience as a full time safety assessment project team representative, preferably with a mix of research, exploratory development and full development teams including experience of biological products
o Principal level: At least 5 years experience as a senior level safety assessment PTR and internal recognition as an opinion leader in one or more aspects of safety assessment, or the equivalent experience in a similar external organization. Experience of biologics safety assessment required.
2. Advanced knowledge of the many scientific disciplines involved in biopharmaceutical drug safety assessment and the relevant laboratory tools and procedures related to safety assessment and risk management, including PK-PD aspects of study design and data interpretation
3. Documented expertise in scientific and technical problem-solving in an international, multi-disciplinary, project-driven environment.
4. Proficient with full range of techniques used in job and core area?especially with communication and negotiation with global health authorities.
5. Detailed knowledge of drug development processes and worldwide regulatory guidelines and procedures.
6. Ability to manage conflicting expectations in a matrix environment.
7. Proven negotiation skills.
8. Excellent program and project management skills.
9. Team player behavioural attributes.
10. Self-motivated and able to operate independently.
11. Ability to coach and advise colleagues in project-related matters (at senior and principal levels). |
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