Principal Associate - QA Batch Disposition

The Principal Associate - QA Batch Disposition role at Lilly is focused on ensuring the quality and compliance of drug and device products through effective oversight of site activities. This position is critical for the final disposition of semi-finished and finished drug combination products, ensuring that high-quality medicines are released to the market in a timely manner. The role involves working in a new state-of-the-art manufacturing facility in Concord, North Carolina, which is being developed to enhance the company's manufacturing capacity for injectable medications and device assembly.