Bristol Myers Squibb is seeking an Associate Director for their GRS-CMC Cell Therapy team in Warsaw, Poland. The role focuses on providing regulatory expertise for CMC activities across the product lifecycle, requiring strong project management and communication skills
Job Summary
The GRS-CMC Associate Director serves as the primary interface between Global Regulatory Sciences and Global Product Development for cell therapy products.
This role involves independently managing complex projects, providing strategic guidance on global regulatory requirements, and leading Health Authority meetings.
Bristol Myers Squibb offers a wide variety of competitive benefits and programs designed to support employee goals both at work and in personal lives.
Matching Summary
Match Score: 85
Bristol Myers Squibb is seeking an Associate Director for their GRS-CMC Cell Therapy team in Warsaw, Poland. The role focuses on providing regulatory expertise for CMC activities across the product lifecycle, requiring strong project management and communication skills.
Salary
Base: zł361,740 - zł438,337; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Wide variety of competitive benefits and programs
Skills & Requirements
Must-have
8+ years pharmaceutical industry experience
5+ years CMC regulatory strategy
Knowledge of cell therapy and biologics
Global regulatory submission management
Manufacturing change control assessment
Nice-to-have
Experience with small molecules and devices
Strong project management skills
Ability to lead matrix teams
Continuous improvement mindset
Cross-functional collaboration
Key Requirements
Minimum BA/BS Degree
8+ years Pharmaceutical industry experience
5+ years CMC regulatory strategy knowledge
Expertise in biological and cell therapy modalities