Lead QA Investigator — Compliance & Production Excellence
Aveva Drug Delivery Systems
A pharmaceutical compliance firm in New York is seeking a Subject Matter Expert for Compliance in Production Operations. In this role, you will ensure adherence to Good Manufacturing Practices (GMP) while assisting in incident investigations and quality assurance documentation. The ideal candidate will have 5-8 years of experience in a regulated environment, excellent problem-solving skills, and knowledge of FDA regulations. This position provides opportunities to mentor colleagues and improve production processes. #J-18808-Ljbffr Aveva Drug Delivery Systems
Vacancy posted 1 day ago
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