Associate - QA Batch Disposition

The Associate QA Batch Disposition role at Lilly is crucial for ensuring the safety and efficacy of drug and device products through effective quality oversight. This position is responsible for the final disposition of semi-finished and finished drug combination products, ensuring compliance with Good Manufacturing Practices (GMP) and supporting the startup of a new state-of-the-art manufacturing facility in Concord, North Carolina. The role involves reviewing and approving GMP documents, maintaining quality systems, and contributing to the overall site readiness plan.