QC Associate Job at Teva Pharmaceuticals – Apply Now
About Teva Pharmaceuticals
At Teva Pharmaceuticals, we are dedicated to making good health more affordable and accessible globally, striving to improve the lives of millions by providing innovative healthcare solutions. With a presence in nearly 60 countries and a diverse workforce from various backgrounds, we are at the forefront of manufacturing generic medicines. Our products are essential for millions of individuals as we continue to innovate and make a positive impact on society.
Job Title: Quality Control Associate – Bioassay & Potency, GMP (On-site)
Date: Apr 15, 2024
Location: West Chester, United States, Pennsylvania, 19380
Company: Teva Pharmaceuticals
Job Id: 55397
The Bioassays and Potency Analysis group at Teva Pharmaceuticals is seeking a Quality Control Associate to perform bioassay, potency, and impurities testing activities in a GMP-compliant QC laboratory. This role supports pre-clinical studies and clinical development for biological products, with responsibilities including method qualification, validation, and transfer while ensuring adherence to regulatory compliance standards.
How you’ll spend your day
- Release and stability testing including cell-based bioassays, ID ELISA, potency ELISA, impurities ELISA.
- Method qualification, validation, and transfer.
- Laboratory investigations (e.g., deviations, Out of Specification, Out of Trend results).
- Management of standard operating procedures, work instructions, protocols, reports, and standard practices.
- Contribution to maintaining a compliant, safe working environment by adhering to ICH, GMP, and safety regulations.
- Participation in internal and external audits, inspections, and regulatory assessments.
Your experience and qualifications
Quality Control Associate (9): Bachelor’s degree in Biochemistry or Biology + 1 year of experience in the (Bio)pharmaceutical industry with bioassays/potency assays.
Senior Quality Control Associate (10): Bachelor’s degree in Biochemistry or Biology + 3 years of experience -OR- Master’s degree + 1 year of experience.
Quality Control Associate Scientist (11): Bachelor’s degree in Biochemistry or Biology + 5 years of experience -OR- Master’s degree + 3 years of experience.
Enjoy a more rewarding choice
We provide a competitive benefits package that includes Medical, Dental, Vision, and Prescription coverage, as well as Disability and Life Insurance, Paid Time Off, and more.
Reports To: Senior Manager, R&D Team Leader
Keywords: QC Associate Job at Teva Pharmaceuticals – Apply Now. Quality Control Associate, Bioassay, Potency, GMP, Pharmaceutical Industry, Biochemistry, Biology, Teva Pharmaceuticals
