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The Associate Manager, Quality Assurance (MES) supervises a QA team, ensuring compliance and quality in manufacturing processes, managing documentation approvals, and participating in regulatory audits. They focus on meeting goals for MES implementation and provide leadership in improving QA performance.

As a Quality Control Technical Resources Specialist, you will manage validation and qualification projects, collaborate with teams, write protocols, control test procedures, and communicate with management and partners on progress and discrepancies. You will thrive in a fast-paced environment, handling multiple tasks and driving scientific improvements.

Fill/Finish Operators at Regeneron support aseptic filling manufacturing processes, operating both manual and automated equipment. Responsibilities include maintaining equipment, ensuring stock levels, cleaning for line clearance, completing batch records, assisting Biotech Production Specialists, and training new employees. Candidates are expected to adhere to cGMP standards and may need to travel for training purposes.