Senior Validation Lead – GMP Compliance & Process Validation

A global biopharmaceutical company in Rockville, Maryland seeks a Principal Specialist, Validation. This role involves managing complex GMP validation projects ensuring compliance with regulatory standards. Requires a Bachelor's degree, 6 years of related experience, and leadership in project management. Key responsibilities include overseeing validation activities, developing SOPs, and providing training. The position offers competitive compensation and a collaborative environment focused on innovation and compliance. #J-18808-Ljbffr