GMP Documentation Specialist - QC (Hybrid)

A leading biopharmaceutical company in Summit, NJ, seeks a candidate to support compliance and technical document management in CAR T manufacturing. Tasks include authoring GMP documents, managing document management systems, and conducting investigations. A Bachelor's degree in Science and 4 years in a regulated environment are required. This hybrid position offers a starting hourly rate of $27 to $29.08 and requires strong attention to detail and collaboration skills. #J-18808-Ljbffr