Knowledge of biologics and cell therapy development
Bristol Myers Squibb is seeking an Associate Director for their GRS-CMC team in Warsaw, Poland, responsible for leading regulatory CMC strategies and managing complex projects in the biologics sector. The role requires significant experience in the pharmaceutical industry, particularly in regulatory affairs, and offers opportunities for professional growth in a supportive and innovative work environment
Job Summary
The role involves developing global regulatory CMC strategies and partnering with stakeholders to execute them in alignment with business priorities.
Candidates will serve as the primary interface between Global Regulatory Sciences and Global Product Development, managing complex manufacturing change controls.
Bristol Myers Squibb offers a wide variety of competitive benefits and programs to support employees' goals both at work and in their personal lives.
Matching Summary
Match Score: 85
Bristol Myers Squibb is seeking an Associate Director for their GRS-CMC team in Warsaw, Poland, responsible for leading regulatory CMC strategies and managing complex projects in the biologics sector. The role requires significant experience in the pharmaceutical industry, particularly in regulatory affairs, and offers opportunities for professional growth in a supportive and innovative work environment.
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 biologics and cell therapy development
Experience with global regulatory submissions
Ability to lead matrix teams
Nice-to-have
Strong project management skills
Innovative problem-solving abilities
Cross-functional team collaboration
Continuous improvement mindset
Excellent oral and written communication
Key Requirements
Minimum BA/BS Degree
8+ years Pharmaceutical industry experience
5+ years CMC regulatory strategy knowledge
Expertise in biologics, cell therapy, or small molecules