GMP Document Control Specialist – 2nd Shift

A biotechnology company is seeking a QA Document Control Specialist I/II/III in Raritan, NJ to support document management in a GMP environment. The ideal candidate will have a Bachelor's degree in a relevant field and at least 2 years of related experience, preferably in aseptic manufacturing. Responsibilities include ensuring compliance within document systems, supporting batch documentation, and collaborating with cross-functional teams. This position offers a comprehensive benefits package, including medical, 401(k), and paid leave policies. #J-18808-Ljbffr