Job Description & How to Apply Below
This position at AbCellera offers you an opportunity to apply your extensive GxP experience to lead Quality oversight in our biological Drug Substance facility. You will partner with multiple teams to ensure operations consistently meet industry regulations and best practices, enhancing patient outcomes through effective quality management.
Key Responsibilities:
• Manage Quality oversight during all GMP operations
• Facilitate timely release of materials for clinical programs
• Conduct investigations to eliminate quality issues
• Lead Quality partnerships for tech transfers and new products
• Champion best practices in continuous improvement initiatives
Requirements:
• Minimum 12 years GxP experience, 5 years in leadership roles
• Strong knowledge of pharmaceutical regulations and practices
• Experience building and leading effective Quality teams
• Hands-on with Drug Substance manufacturing processes
• Proficient with ERP, eQMS, and LIMS systems
Drive quality initiatives that contribute to breakthrough medicines at AbCellera.
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Position Requirements
10+ Years
work experience
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