CQV Specialist II Cell Therapy Manufacturing Operations

A leading biotechnology company in Raritan, NJ, is seeking a CQV Specialist II to provide essential support for the Commissioning, Qualification, and Validation processes within the cGMP manufacturing plant. The role requires a Bachelor's Degree in a relevant field and at least 4 years of experience in aseptic manufacturing or quality assurance. Key responsibilities include executing validation protocols, managing complex CQV projects, and ensuring compliance with regulatory requirements. This position offers a competitive salary and comprehensive benefits package. #J-18808-Ljbffr