Description
Bristol Myers Squibb is seeking an Associate Director for Finished Drug Product (FDP) certification of biological products for the EU/EEA and ROW markets. The role involves operating with significant autonomy, ensuring consistent, risk-based decision-making, and aligning quality standards across various manufacturing sites. The Associate Director will provide conceptual and practical expertise in QP requirements, resolve complex problems, and lead the implementation of the Quality Management System. Key responsibilities include certifying finished product batches, performing release duties, acting as a primary contact for product/brand-related queries, building collaborative relationships, chairing product disposition governance forums, supporting new product introductions, participating in product recall processes, and continuously maintaining familiarity with manufacturing and testing requirements.
