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16 days old

Director, Quality Assurance

Teva Pharmaceuticals
Davie, FL US
Company InfoIf youre like people at Teva, you dare to be different. Were making well-being a way of life for our customers and our colleagues. Join us in helping to make healthcare more accessible to more patients, while supporting one of the most innovative teams in the industry. Tevas Davie and S...
Company InfoIf youre like people at Teva, you dare to be different. Were making well-being a way of life for our customers and our colleagues....
1+ months

Associate Director, Quality Compliance, Americas

Teva Pharmaceuticals
Parsippany, NJ US
Company InfoTeva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's ...
Company InfoTeva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and...
23 days old

Principal Medical Writer

Teva Pharmaceuticals
West Chester, PA US
A Principal Writer in the Global Regulatory Medical Writing and Submission Management organization at Teva provides basic-level oversight and guidance, as well as resource management, for the direct medical-writing support given to Clinical Specialty Development (and other departments as appropriate...
A Principal Writer in the Global Regulatory Medical Writing and Submission Management organization at Teva provides basic-level oversight and...
23 days old

Senior Manager Global Reg Medical Writing

Teva Pharmaceuticals
West Chester, PA US
  A Senior Manager in the Global Regulatory Medical Writing and Submission Management organization at Teva provides leadership,  oversight and guidance, as well as resource management, for the direct medical-writing support given to Clinical Specialty Development (and other departments as appropria...
  A Senior Manager in the Global Regulatory Medical Writing and Submission Management organization at Teva provides leadership,  oversight and...
26 days old

Upstream Manufacturing Associate

Teva Pharmaceuticals
West Chester, PA US
  Hours for position are 1st shift Sunday through Thursday and occasional holiday work to meet manufacturing process schedule.     Job Responsibilities: Responsible for product-related operations in cell culture/fermentation and bioreactor operations. Primarily focused on cell culture activities...
  Hours for position are 1st shift Sunday through Thursday and occasional holiday work to meet manufacturing process schedule.     Job...
7 days old

Procedural Documents Intern

Teva Pharmaceuticals
West Chester, PA US
Teva Pharmaceuticals is looking to fill a Procedural Documents intern role in West Chester, PA. Seeking an undergraduate or graduate student with a background in Digital Media, Library Sciences, Graphic Design, Information Systems, Communications, Math, Data Sciences, Engineering, Pharmaceutical Sci...
Teva Pharmaceuticals is looking to fill a Procedural Documents intern role in West Chester, PA. Seeking an undergraduate or graduate student with...
7 days old

Bayesian Method Development Intern

Teva Pharmaceuticals
West Chester, PA US
Teva Pharmaceuticals is looking to fill a Bayesian Method Development Intern role in West Chester, PA. Teva Pharmaceuticals is seeking a graduate student with a background in statistics/biostatistics or related field. The project will result in development of innovative statistical method applicatio...
Teva Pharmaceuticals is looking to fill a Bayesian Method Development Intern role in West Chester, PA. Teva Pharmaceuticals is seeking a graduate...
7 days old

Biological Researcher I

Teva Pharmaceuticals
West Chester, PA US
Develop stage appropriate downstream process for Tevas biologics pipeline and generate material for formulation development and toxicology study Evaluate new purification technologies to improve the efficiency of biologics manufacturing process and reduce cost of good Design fit-for-purpose purifi...
Develop stage appropriate downstream process for Tevas biologics pipeline and generate material for formulation development and toxicology...
28 days old

Upstream Process Development Scientist

Teva Pharmaceuticals
West Chester, PA US
We are seeking a highly motivated individual to join us as Scientist, Upstream Process Development within Biologics CMC, located at West Chester, PA. The successful candidate independently designs, executes and interprets complex laboratory experiments with priorities set by supervisor to achieve pr...
We are seeking a highly motivated individual to join us as Scientist, Upstream Process Development within Biologics CMC, located at West Chester,...
12 days old

Senior Director Clinical Development (Pain)

Teva Pharmaceuticals
West Chester, PA US
The Senior Director of Clinical Development in the Pain TA,  serves as the Clinical Project Leader (CPL) physician and provides clinical leadership and medical monitoring of clinical studies. The Senior Director is responsible for supporting assigned drug development projects including the developme...
The Senior Director of Clinical Development in the Pain TA,  serves as the Clinical Project Leader (CPL) physician and provides clinical...
5 days old

Medical Outcomes Liaison

Teva Pharmaceuticals
Scranton, PA US
  The purpose of the Medical Outcomes Liaison (MOL) position at Teva Pharmaceuticals is to be an expert of managed care and health systems delivery of patient care with high scientific and medical acumen in therapeutic areas of interest to Teva Pharmaceuticals USA. The purpose will be achieved with...
  The purpose of the Medical Outcomes Liaison (MOL) position at Teva Pharmaceuticals is to be an expert of managed care and health systems...
7 days old

Regulatory Affairs Strategist Intern

Teva Pharmaceuticals
West Chester, PA US
Teva Pharmaceuticals is looking to fill a Regulatory Affairs Strategist role in West Chester, PA. For this role, Teva Pharmaceuticals is seeking an undergraduate or graduate student in the field of science, pharmacy or related discipline. As an intern, you will gain an exposure to clinical developme...
Teva Pharmaceuticals is looking to fill a Regulatory Affairs Strategist role in West Chester, PA. For this role, Teva Pharmaceuticals is seeking...
2 days old

Biological Researcher I

Teva Pharmaceuticals
West Chester, PA US
Company InfoTeva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's ...
Company InfoTeva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and...
8 days old

Senior Principal Device Engineer

Teva Pharmaceuticals
Salt Lake City, UT US
  The Sr. Principal Device Engineer, Combination Product and Device is responsible for design, development, implementation, and analysis of medical devices as well as serving as SME for sustaining engineering for products manufactured at the site. Performs engineering design evaluations. May develo...
  The Sr. Principal Device Engineer, Combination Product and Device is responsible for design, development, implementation, and analysis of...
2 days old

Principal Data Scientist, Translational Statistics

Teva Pharmaceuticals
West Chester, PA US
Teva's global R&D is hiring a Principal Scientist or Manager to join the Translational Statistics and Bioinformatics team.  This will be a critical position responsible and accountable for designing and analyzing Translational Medicine (TM) studies and serving as the point person for scientific ...
Teva's global R&D is hiring a Principal Scientist or Manager to join the Translational Statistics and Bioinformatics team.  This will be a...
29 days old

Associate Director Medical Writing, Biometrics

Teva Pharmaceuticals
West Chester, PA US
An Associate Director, in Global Regulatory Medical Writing, provides advanced-level oversight and guidance, as well as resource management for the direct medical-writing support given to Clinical Specialty Development (and other departments as appropriate) in the production of clinical research doc...
An Associate Director, in Global Regulatory Medical Writing, provides advanced-level oversight and guidance, as well as resource management for...

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