Who we are
Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with.
The opportunity
The Raw Materials Analysis group strives to deliver creative medicines to patients through performance of sampling, testing and release of controlled materials within a GxP-compliant QC laboratory to support development of biological products manufactured in a GMP production facility. The incumbent should possess a practical understanding of bio-pharmaceutical drug development and GxP requirements as knowledge of local, regional and global regulatory compliance (ICH, GMP, EPA, OSHA, DEA, etc) are integral responsibilities of this position.
Travel Requirements : none
Location: West Chester, PA
RELOCATION ASSISTANCE AND WORK VISA SPONSORSHIP IS NOT AVAILABLE
How you'll spend your day

• Sampling, testing and release of raw materials (e.g. executing testing, results analysis, peer review of data, etc.)
• Method qualification and validation, as required.
• Laboratory investigation (e.g. deviations, Out of Specification, Out of Trend results), Change Controls, Deviations and CAPA (Corrective Action/Preventive Action) management, as required.
• Management of standard operating procedures, work instructions, protocols, reports, and standard practices.
• Actively contribute to the maintenance of a compliant, clean, safe working environment (e.g. records, instruments, equipment, materials, reagents, quality systems etc.) in the laboratories by maintaining compliance with applicable ICH, GMP and safety regulations.
• Participate in internal and external audits, inspections, regulatory assessments, and filings.

Your experience and qualifications
Quality Control Associate (9)
Bachelor's degree, preferably in Chemistry, Biochemistry or Biology, from an accredited college or university 1 year in the (Bio)pharmaceutical industry with Raw Material Testing and sampling.
Senior Quality Control Associate (10)
Bachelor's degree, preferably in Biochemistry or Biology, from an accredited college or university 3 years of experience in the (Bio)pharmaceutical industry with Raw Material Testing and sampling -OR- Master's degree, preferably in Biochemistry or Biology, from an accredited college or university 1 year of experience in the (Bio)pharmaceutical industry with bioassays/potency assays
Quality Control Associate Scientist (11)
Bachelor's degree, preferably in Biochemistry or Biology, from an accredited college or university 5 years of experience in the (Bio)pharmaceutical industry with Raw Material Testing and sampling -OR- Master's degree, preferably in Biochemistry or Biology, from an accredited college or university 3 years of experience in the (Bio)pharmaceutical industry with Raw Material Testing and sampling.
Enjoy a more rewarding choice
We offer a competitive benefits package, including Medical, Dental, Vision, and Prescription coverage starting on the first day. We also offer Disability and Life Insurance, Paid Time Off, 13 paid Holidays, 6% match on the 401(k), Employee Stock Purchase Plan, and Tuition Assistance
Reports To
Senior Manager, R&D Team Leader
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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.