Senior QA Specialist, Biotech GMP & Vendor Documentation

A biopharmaceutical company in Verona, Wisconsin is seeking a Quality Assurance professional to provide support for development and clinical programs. The ideal candidate will have at least 5 years of experience in a GMP-regulated environment and hold a BS/BA in a scientific field. Responsibilities include reviewing vendor documentation, collaborating with internal departments, and ensuring compliance with quality standards. Excellent communication skills are essential as you will work closely with multiple organizations to maintain quality assurance in the clinical pipeline. #J-18808-Ljbffr