QA Document Control Specialist – 2nd Shift (GMP)

A biotechnology company is seeking a QA Document Control Specialist I/II/III in Raritan, NJ. This role involves ensuring compliance within document management in a sterile GMP environment. Candidates should have a Bachelor's degree in a relevant field and a minimum of 2 years of experience in quality assurance or related areas. Key responsibilities include managing document workflows, reviewing SOPs, and supporting GMP requirements. Excellent communication and organizational skills are essential. #J-18808-Ljbffr