About this role
Associate Director, GMP QA Operations at Dyne Therapeutics. Location: Waltham, Massachusetts, United States. Role: overseeing manufacturing, leading investigations, managing systems Requirements: Bachelor's in engineering/science (Master's preferred), 8+ years in cGMP environment and 5+ years in QA, experience overseeing CMOs/CDMOs, knowledge of FDA/EMA regulations, GxP QA systems, strong communication and decision-making skills. Category: Quality Assurance Seniority: Senior Level Tools: Microsoft Office, SmartSheet, Veeva Commitment: Full Time Workplace: Onsite Languages: English