CGMP Quality Documentation Specialist

A leading pharmaceutical company is seeking a Quality Control Document Specialist to manage Quality Control documentation and ensure compliance with regulations. Responsibilities include creating specifications and procedures, supporting audits, and collaborating with teams. The ideal candidate holds a Bachelor's in a relevant field and has at least 2 years' experience in Quality Control. Strong communication and time management skills are essential for success in this role. #J-18808-Ljbffr