Quality Documentation Specialist I (QMS & CGMP)

A pharmaceutical company is seeking a Quality Assurance Documentation Specialist I to ensure compliance with documentation processes. The role involves maintaining documents for the Quality Management System, issuing batch records, and supporting audits. Candidates should have 2-5 years of experience in a cGMP environment and possess excellent communication and organizational skills. An associate degree in a related field is preferred. #J-18808-Ljbffr