Quality Director, CGMP & Compliance

A growing pharmaceutical company in New Jersey is seeking an experienced Associate Director, Quality to lead the U.S. Quality function. This high-visibility role demands overseeing compliance activities, managing CGMP audits, and maintaining product quality. Candidates must possess a B.S. in a science discipline and have at least 10 years of relevant experience. Join a culture that embraces diversity and values the contributions of each employee. #J-18808-Ljbffr