Cardinal Health is seeking a Quality Assurance Specialist (QAS) for an FDA-regulated drug manufacturing facility in Columbus, OH. The role focuses on CGMP documentation, product release, and quality system management to ensure compliance with 21 CFR 212.
The role requires 2–4 years of experience, proficiency in MS Excel and MS Word, and strong attention to detail. Night shifts and filing/system management experience are preferred, with opportunities for process improvement and collaboration with
#J-18808-LjbffrCGMP QA Specialist — Night Shift Drug Manufacturing in ky at Unknown Company
This position is listed as full time and onsite.