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Date: Jun 10, 2021

Location: West Chester, Pennsylvania, US, 19380

Company: Teva Pharmaceuticals

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!

Teva’s 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.

Job Description

  In this role you will lead and coordinate biologics analytical testing to support detailed product characterization and process development studies. You will utilize expertise and technical leadership skills to resolve issues and contribute to CMC project teams. This role also includes engaging an inclusive/ diverse/ innovative/ creative culture in delivering business results. 


Essential Job Duties and Responsibilities:

  • Conduct biologics analytical testing using LC-MS for product and process characterization
  • Perform MS analyses including, but not limited to, intact/reduced mass, peptide mapping, glycan analysis, primary sequence confirmation and elucidation, and determination of post-translational modifications
  • Operate and maintain equipment in a qualified state
  • Document experiments in electronic notebooks and technical protocols/reports to ensure data integrity
  • Serve as analytical representative and technical SME on CMC project teams
  • Author analytical method and characterization sections of regulatory submissions
  • Interact with internal and external contacts in providing solutions to complex scientific/technical issues associated with specific projects



What you will bring to this role

  • Master’s degree in Analytical Chemistry, Biochemistry or related discipline with a minimum of 5 years of lab experience in biotech/biopharma or CRO industry OR a PhD degree in Analytical Chemistry, Biochemistry or related discipline with a minimum of 3 years of lab experience in biotech/biopharma or CRO industry
  • Minimum 2 years of experience in analytical method development using HPLC, UPLC, and MS platforms and software packages


Preferred Qualifications

  • 1 year experience LC-MS experience with mAbs and fusion proteins
  • Experience in analytical method qualification experience
  • Experience in regulatory experience with analytical method and data sections


Research & Development

Sub Function

Drug Analysis and Formulation

Reports To

Associate Director, Analytical Sciences & Operations, Biologics CMC

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’s Equal Employment Opportunity Commitment

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.

Nearest Major Market: Philadelphia