GMP QA Specialist II: Lead Compliance & Audits

A leading biotechnology company in Indiana is seeking a QA Specialist II to perform day-to-day quality assurance activities ensuring compliance with FDA regulations. This role involves managing GMP documentation, supporting audits, and driving continuous improvements. The ideal candidate holds a degree in a science-related field and has 3-5 years’ experience in Quality Assurance. Competitive compensation and benefits are offered. #J-18808-Ljbffr