CGMP QA Specialist — Night Shift Drug Manufacturing
Listed on 2026-10-09
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Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist, Production QC/QA
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
We are currently recruiting a CGMP QA Specialist — Night Shift Drug Manufacturing for our team in KY, United States.
The advertised compensation is 67.000 - 95.000.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the CGMP QA Specialist — Night Shift Drug Manufacturing role in the description above.
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