Lead QA: Batch Disposition & Compliance

A biopharmaceutical company located in North Carolina is seeking a professional responsible for managing Batch disposition processes. The ideal candidate will possess over 15 years of experience in a cGMP regulated environment and have expertise in Quality Systems. Key responsibilities include tracking batch documentation, collaborating with various teams, and ensuring compliance with cGMP guidelines. This role supports both commercial and clinical batch dispositions and involves direct interaction with clients and internal teams.
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