Senior QA Specialist, GMP & Documentation

A leading biopharmaceutical company in Verona, WI seeks a Quality Assurance Specialist II. This role supports ongoing drug development programs and involves reviewing documentation, ensuring compliance with GMP, and collaborating across departments. The ideal candidate will hold a relevant degree, possess at least 3 years of Quality Assurance experience, and demonstrate knowledge of drug GMP regulations. Competitive salary and benefits are offered, and candidates must be authorized to work in the US. #J-18808-Ljbffr