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.
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📌 Associate Director QA Operations at AbCellera (British Columbia)
🏢 AbCellera
📍 British Columbia