Senior QA Specialist: cGMP Audits & Pharma Growth

A leading CDMO company in Somerset, NJ, is seeking a Senior Quality Assurance Specialist to ensure compliance with cGMP and other regulations within a fast-paced manufacturing environment. The role involves routine auditing, providing support to production teams, and participation in quality system reviews. Candidates must have a Bachelor’s degree and at least three years in pharma QA. The position offers a competitive salary and benefits package, along with opportunities for career growth within an innovative organization. #J-18808-Ljbffr