Bristol Myers Squibb is seeking an Associate Director for their Cell Therapy Network CQV, responsible for overseeing the strategy for Commissioning, Qualification, and Validation across various manufacturing sites. The role requires extensive experience in biologics or cell therapy GMP manufacturing and is designed for candidates who can lead cross-functional collaborations and ensure regulatory compliance
Job Summary
The Associate Director, Cell Therapy Network CQV is responsible for the network strategy for equipment/facility/utility Commissioning, Qualification, and Validation, encompassing internal CT manufacturing sites and engagement with external CMOs.
This role will partner cross-functionally with site CQV leads, site equipment owners, Cell Therapy network Digital Plant leaders, the BMS QMS Qualification Global Process Owner, and CTTO Global Equipment Owners.
Bristol Myers Squibb offers a wide variety of competitive benefits, services, and programs that provide employees with resources to pursue their goals, both at work and in their personal lives.
Matching Summary
Match Score: 85
Bristol Myers Squibb is seeking an Associate Director for their Cell Therapy Network CQV, responsible for overseeing the strategy for Commissioning, Qualification, and Validation across various manufacturing sites. The role requires extensive experience in biologics or cell therapy GMP manufacturing and is designed for candidates who can lead cross-functional collaborations and ensure regulatory compliance.
Salary
Base: $164,260 - $218,947; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Health coverage, Wellbeing Support, Financial Well-being and Protection, Work-life benefits
Skills & Requirements
Must-have
Cell Therapy manufacturing support
GxP compliance
ICH guidelines knowledge
Validation lifecycle frameworks
Cross-functional collaboration
Nice-to-have
Project management tools utilization
Lean Six Sigma tools
Strategic thinking and problem-solving
Interpersonal and team building skills
Key Requirements
15+ years w/ B.S. or 12 years w/ M.S. or 8 years w/ Ph.D. experience
B.S., M.S., or Ph.D. in Engineering or related discipline
Biologics or cell therapy GMP manufacturing experience
Strong understanding of CMC regulatory requirements