Onsite GMP QA & Regulatory Compliance Lead

A biopharmaceutical company in Indiana is seeking a QA Regulatory Compliance Specialist to enhance Quality Systems and ensure regulatory compliance in a GMP-regulated environment. The ideal candidate will have over 8 years of experience in biopharmaceutical manufacturing with a focus on QA compliance programs. Responsibilities include supporting audits, maintaining inspection readiness, and driving quality improvement initiatives. This is a contract position, requiring the ability to work onsite and collaborate with teams across the organization. #J-18808-Ljbffr