Senior QAV Specialist: Biopharma Validation & Quality
Planet Pharma
Planet Pharma in Bedford, MA, is seeking a QAV specialist to provide onsite support at the AM805 tech transfer project. You will review and approve validation documents and BMRAM work orders, representing QAV in cross‑functional project meetings and ensuring compliance with GMP requirements. The role requires a BS in engineering or a related science, hands‑on validation and data integrity experience, knowledge of FDA/EMA regulations, and strong technical writing and documentation review skills. #J-18808-Ljbffr Planet Pharma
Vacancy posted 17 hours ago
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