15 days old


West Chester, PA 19380

Company Info

Teva 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 largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas. We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

Job Description

Tevas Global Research & Development (R&D) organization is devoted to the development of new medicines, devices and combination products that provide meaningful therapeutic benefit to patients worldwide. Combining creativity, scientific rigor and our extensive knowledge on a broad range of technologies, our scientists, engineers, medical doctors and project leaders across the globe use their expertise to innovate novel biologics, biosimilars, small molecule specialty medicines, generics and over-the-counter therapies.


Located in West Chester, PA, Biologics CMC is a division of Teva Pharmaceuticals responsible for the development of Biologics. The rapidly growing staff of Biologics CMC specializes in the development of innovative biologics, biosimilars, and extended half-life bio-betters. We currently are developing products in various stages of clinical development from IND through BLA filing. Drug Product Development and Operations (DPDO) is a function within Biologics CMC dedicated to development of formulation, drug product configuration and manufacturing process of the non-clinical and the clinical drug product lots. You will play a key role in DPDO to support the formulation development of Teva innovative and biosimilar product pipeline for manufacture into drug product.


As a Scientist, you will lead projects and studies, execute analytical test methods, organize the data and author related technical documents, all in compliance with applicable policies. Additionally, you will lead activities related to development of a high throughput platform to increase efficiency in formulation development. You will also serve as owner for multiple analytical instrumentation that supports formulation development, which includes writing supporting SOPs, working as subject matter expert (SME), training as needed and maintaining the instrumentation. 



  • Design and execute the experiments based on QbD principles, evaluate quality of the data and work on ways to improve data analysis and presentation formats.
  • Develop efficient platform processes for formulation and process development of drug products for innovative biologics.
  • Develop and verify high throughput methods and integrate in the development process of a formulation and/or drug product.
  • Represent as DP lead for selected projects and directly participate in the CMC, other sub-team and site-wide meetings as needed. 
  • Design and develop efficient methods of lyophilization for biologic drug products and work on tech transfer and scale-up issues as needed. 
  • Transfer and perform routine analytical methods including chromatographic, electrophoretic, biophysical and other general test methods.  
  • Author protocols, reports, technical documents and other relevant CTDs for regulatory filings including IND/IMPD and marketing applications as needed.
  • Coordinate with external contracting organizations to accomplish project goals as needed and serve as point of contact on the outsourced activities.
  • Support working on novel methodologies for development of high concentrated protein formulations and extractables and leachables program. 
  • Assist in the set-up and maintenance of a new state of the art lab including ownership of instrumentation, writing SOPs and serve as subject matter expert for the related technologies.
  • Effectively work in collaboration with different functions in the CMC as well as other non-technical teams on site to facilitate routine operations.


What you will bring to the role:

  • Bachelors in chemistry, biology, pharmaceutical sciences, biochemistry, chemical engineering or other related discipline with a minimum of 10 years of experience in analytical and/or development experience with protein molecules, or Masters in a related discipline with a minimum of 8 years, or Ph.D. in a similar discipline with a minimum of 1 year of experience in above.
  • Minimum 3 years hands-on experience in analytical testing using physical and biochemical, characterization methods, such as general appearance, opalescence, osmolality, MFI, HIAC, viscosity, HPLC, DLS, DSC, and CD spectroscopies.

Preferred Qualifications:

  • Experience in high throughput experiments and/or development of high concentrated protein formulations.
  • Experience in application of a statistical software (eg. JMP), or implementation of QbD elements. 
  • Highly motivated individual, with ability to work in a team environment and build productive relationships within or across departments.
  • Ability to troubleshoot and determine creative solutions to achieve better processes.
  • Experience in GMPs and/or writing of regulatory submission documents. 
  • Excellent planning, verbal and written skills. Good document practices.
  • Proficient in Microsoft Office Suite of Programs.


Research & Development

Sub Function

Drug Analysis and Formulation

Reports To

Associate Director, R&D

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.  


Posted: 2021-03-25 Expires: 2021-04-24

Join us at the forefront of pharmaceutical research and production. With state-of-the-art facilities, highly skilled colleagues, and a high-powered organizational culture, Teva offers you countless possibilities to make a real difference in people's lives and add value to your career.

Before you go...

Our free job seeker tools include alerts for new jobs, saving your favorites, optimized job matching, and more! Just enter your email below.

Share this job:


Teva Pharmaceuticals
West Chester, PA 19380

Join us to start saving your Favorite Jobs!

Sign In Create Account
Powered ByCareerCast