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 processesDrive batch record reviews for timely GMP material releaseLead CAPAs and root cause investigations for ongoing improvementEnsure material qualification and phase release of componentsShape Quality policies and maintain inspection readinessRequirements:12+ years of GxP industry experience, 5 years in quality leadershipIn-depth knowledge of FDA, Health Canada, and ICH regulationsProven track record in building high-performance Quality teamsExperience in biological Drug Substance and aseptic manufacturingEffective communicator with both technical and non-technical teamsElevate your career by ensuring quality in life-saving medicines at AbCellera.#J-18808-Ljbffr

📌 Associate Director Qa Operations At Abcellera (Vancouver)
🏢 AbCellera
📍 Vancouver