QA Documentation Specialist — GMP & Compliance

A leading pharmaceutical company in Rahway, NJ, is seeking an Associate Technician for their Document Control Center. The role involves managing the printing, issuance, and archival of GMP documentation, ensuring compliance with quality standards. The ideal candidate should hold a diploma in a relevant field and have basic GMP knowledge along with 1-3 years of experience in pharmaceutical manufacturing. This is a temporary position with opportunities for problem-solving and continuous improvement within the company's framework. #J-18808-Ljbffr