Accurately complete and verify batch records, logbooks, inventory transactions, forms, and other required documentation in compliance with cGMP and data integrity requirements, ensuring the accuracy of materials, components, quantities, identification, and status information, and promptly reporting any discrepancies, errors, or questionable entries to the appropriate Team Lead or Supervisor. Backed by more than $100 million in recent investments, the Greenville operation features fit‑for‑scale infrastructure, potent handling capabilities, and a strong regulatory track record, making it a critical part of Catalent's global network for advancing complex oral drug programs from development to market.