Senior QMS Lead - Production Compliance & Audits

A leading pharmaceutical company in Pennsylvania seeks a Quality Management System Specialist. This role focuses on ensuring compliance with cGMP, USFDA, and other regulatory requirements while implementing QMS practices in the Production department. Responsibilities include preparing documentation, monitoring batch execution, and providing training to staff. Ideal candidates have a B.Pharm/M.Pharm and 6-10 years of experience in a regulated manufacturing environment, with a strong knowledge of cGMP and USFDA guidelines. #J-18808-Ljbffr