Overview The QA Specialist 3 ensures compliance with FDA regulations (21 CFR Part 820), GMP standards, ISO/ASTM requirements, and internal protocols by overseeing in-process and finished-goods quality testing for nitrile glove manufacturing. This role is responsible for inspections, sampling, AQL testing, packaging and pallet quality verification, and generation of Certificates of Analysis (CoAs). The QA Specialist 3 supports continuous improvement, maintains product integrity, and ensures comp