QC Documentation & CGMP Compliance Specialist

A pharmaceutical company based in Monroe, North Carolina, is seeking a Quality Control Document Specialist. In this role, you will manage Quality Control documentation and ensure compliance with regulations while supporting audits and cross-functional teams. Candidates should have a Bachelor’s degree in a relevant field and a minimum of 2 years experience in Quality Control. Excellent communication and attention to detail are essential. This position offers a full-time employment opportunity with a focus on quality and continuous improvement. #J-18808-Ljbffr