QA Director, Radiopharmaceuticals – Site Quality & Compliance

100 Eli Lilly and Company · Indianapolis, United States

Lilly in Indianapolis is seeking a QA Associate Director/Director to lead a multi-shift GMP operation for radioligand production and oversee QA record review, release, and regulatory compliance. The role includes site leadership collaboration, training, and ensuring inspection readiness for global standards.

You will manage QA personnel, develop local procedures, and partner with Technical Services to qualify manufacturing changes, while maintaining a safe, compliant workplace and fostering a