Senior QA Validation Specialist – Cell Therapy GMP

A leading biotechnology company in Raritan, NJ is seeking a QA Validation Specialist III to oversee validation and qualification activities in a sterile GMP environment. The ideal candidate will have at least 4 years of relevant experience and knowledge of cGMP regulations. This role entails reviewing documentation and guiding quality compliance within the cell therapy manufacturing process, offering a competitive salary and benefits package. #J-18808-Ljbffr