Lead Quality initiatives at AbCellera’s Vancouver facility as an Associate Director/Senior Manager, QA Operations. Use your expertise to ensure compliance and operational excellence in biological Drug Substance manufacturing.

Join AbCellera as a key player directing QA operations at our clinical manufacturing site. In this senior role, you'll leverage 12 years of GxP experience, ensuring adherence to regulatory standards while fostering a culture of quality. Your contributions will drive continuous improvement and elevate our quality management across the board.

Key Responsibilities:



• Oversee Quality compliance across GMP manufacturing processes • Drive batch record reviews for timely GMP material release • Lead CAPAs and root cause investigations for ongoing improvement • Ensure material qualification and phase release of components • Shape Quality policies and maintain inspection readiness

Requirements: • 12+ years of GxP industry experience, 5 years in quality leadership • In-depth knowledge of FDA, Health Canada, and ICH regulations • Proven track record in building high-performance Quality teams • Experience in biological Drug Substance and aseptic manufacturing • Effective communicator with both technical and non-technical teams

Elevate your career by ensuring quality in life-saving medicines at AbCellera. #J-18808-Ljbffr

📌 Associate Director QA Operations at AbCellera (Winnipeg)
🏢 AbCellera
📍 Winnipeg