QA Documentation Specialist I

A leading pharmaceutical services company in Madison, Wisconsin, is seeking a QA Specialist I to manage and maintain critical CGMP documentation and processes. The ideal candidate will coordinate client batch record activities and ensure compliance with quality standards. Exceptional organizational, verbal, and written communication skills are essential, along with a strong attention to detail and ability to work efficiently in a fast-paced environment. A high school diploma with extensive GMP experience is required. #J-18808-Ljbffr