QA Finishing Ops Specialist, Pharma Quality & Impact
Listed on 2026-10-07
-
Quality Assurance - QA/QC
Production QC/QA, QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers, Quality Engineering
Grand River Aseptic Manufacturing (GRAM) is seeking a QA Specialist I in Finishing Operations to support cGMP quality systems for terminal sterilization, visual inspection, labeling and packaging of parenteral drugs. You will review batch records, release materials, and ensure documentation compliance throughout finishing operations.
Key requirements include 1–2 years of related experience or equivalent GMP exposure, and proficiency with Word, Excel and Outlook.
Our team is growing, and we are hiring a QA Finishing Ops Specialist, Pharma Quality & Impact in Grand Rapids, MI, United States.
Learn more about the QA Finishing Ops Specialist, Pharma Quality & Impact role in the description above.
We appreciate your interest in this position.
Join Grand River Aseptic Manufacturing Inc. and contribute to our ongoing work.
Take a moment to read everything above and see whether this role is right for you.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).