GMP QA Compliance Lead — Onsite Biopharma

A leading biopharmaceutical company is seeking a QA Compliance Specialist in Indianapolis, IN. The role involves supporting quality systems in a GMP-regulated environment, ensuring inspection readiness, and managing QA compliance programs. The ideal candidate will have at least 8 years of experience in biopharmaceutical manufacturing, with strong knowledge of FDA, ICH, and EU regulations. This position requires excellent communication and problem-solving skills, and a Bachelor's degree in Life Sciences is essential. The role is onsite. #J-18808-Ljbffr