Process Engineer Scientist

Teva Pharmaceutical Industries West Chester , PA 19380

Posted 2 months ago

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!

Around 200 million people worldwide take one of our medicines every day. In the United States, where Teva is the leading generic pharmaceutical company, one out of every nine prescriptions is filled by a Teva product. In the both the UK and Canada, it is one out of every six. In addition, many prescription medications made by other companies include active pharmaceutical ingredients produced by Teva.

Job Description

In your new role you will Lead scale-up and technology transfer for clinical/commercial manufacturing of biologic products.

  • Coordinate downstream process technology transfer of clinical/commercial products to internal or external clinical manufacturing sites. Be the liaison between PD and receiving sites.

  • Lead and execute pilot-scale downstream processing at PD, including tox supply production and consistency runs, with minimal supervision and following safety requirements.

  • Support downstream process development leading to commercialization of recombinant therapeutic proteins products.

  • Support PD team on carrying out equipment gap assessments/manufacturing suitability assessments.

  • Use engineering principles to design novel solutions for process fit in the existing manufacturing facilities.

  • Support manufacturing activities at the internal clinical/commercial manufacturing site as needed

  • Provide process/product impact statements in support of manufacturing deviation investigations as a Subject Matter Expert (SME)

  • Author technical reports for documentation of development and tech transfer activities

Qualifications

What you will bring to the role!

REQUIRED QUALIFICATIONS:

  • Minimum 8 years with a BS or 6 years with an MS, or 2 years with a PhD, of direct experience in the biopharmaceutical/biotech industry

  • Minimum 4 years of experience with design and execution of purification process development for therapeutic proteins products.

PREFERRED QUALIFICATIONS:

  • Direct participation in a biologics product commercialization and Familiarity with the cGMP principles

  • Experienced in using AKTA chromatography systems (both lab and process-scale) and UNICORN software

  • Minimum 2 years of experience in generating experimental protocols, performing data analysis using statistical tools and authoring reports.

  • MS/PhD or Post-doctoral training in Chemical/Biochemical Engineering or in a related life-sciences field

  • Demonstrated ability to author technical documentation for regulatory filings

Function

Research & Development

Sub Function

Drug Analysis and Formulation

Reports To

In process of validation

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

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Process Engineer Scientist

Teva Pharmaceutical Industries