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 Vancouver (Canada)
🏢 AbCellera
📍 Canada