Director, CMC Quality
Vancouver, BCAbCellera: AbCellera is a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology,…
12+ YOECandidates need a life sciences or engineering bachelor's degree, with an MS or PhD preferred, and 12+ years in biopharmaceutical quality, regulatory or manufacturing compliance. Strong global cGMP knowledge, control and comparability strategy expertise, and proven leadership are required.
Leadership, Regulatory compliance, Supply chain management, Good manufacturing practices, Inspection, Chemical engineering
VP, Late-Stage & Commercial Biologics Development
Vancouver, BCAbCellera: AbCellera is a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology,…
18+ YOE8+ MgmtCandidates need a post-secondary degree in a biological or chemical field and 18 to 20+ years in biopharmaceutical process development or CMC, including at least 8 years in leadership. They need a record of taking biologics through PPQ and approval, plus experience with CDMO tech transfers and combination products.
Troubleshooting, Coaching, Process improvement, Quality assurance, Regulatory affairs, Supply chain management
Senior Engineer, Combination Products & Device Development
Vancouver, BCAbCellera: AbCellera is a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology,…
8+ YOECandidates need 8+ years of direct drug delivery or combination product experience, ideally with prefilled syringes or autoinjectors. They also need knowledge of FDA design controls, ISO standards, and working with external device partners.
prefilled syringe, autoinjector, needle safety systems
Director, Combination Products & Device Development
Vancouver, BCAbCellera: AbCellera is a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology,…
15+ YOECandidates need a bachelor's or graduate degree in mechanical, biomedical or chemical engineering, at least 15 years of hands-on device engineering, and deep knowledge of FDA and ISO combination product standards. Management of technical teams and external partners is essential.
Leadership, Regulatory compliance, Coaching, Process improvement, Documentation, Risk management