CQV Specialist I – Cell Therapy Validation & Compliance

A leading biotechnology firm in New Jersey seeks a skilled professional to provide Commissioning, Qualification and Validation support in their cell therapy manufacturing plant. This role entails executing compliance activities, managing complex projects, and collaborating across teams for effective production. Candidates should have a Bachelor’s degree and relevant experience in cGMP environments. The position offers a competitive salary and an extensive benefits package, reflecting the company's commitment to employee well-being and growth. #J-18808-Ljbffr