Pharma Inspection Line Lead – QC & cGMP
Listed on 2026-10-14
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, Quality Control - QC Analysts/Managers
Grand River Aseptic Manufacturing Inc. is seeking an Inspector to oversee inspection tasks and support cGMP compliance in the Finishing area. You will lead inspection operations, train staff, and ensure regulatory standards are met across QA processes.
The role requires knowledge of parenteral product inspection, FDA guidelines, and GMP practices, with proficiency in MS Office and Master Control. OT hours and weekend work may be required.
We are currently recruiting a Pharma Inspection Line Lead – QC & cGMP for our team in Grand Rapids, MI, United States.
Full responsibilities and requirements are described in the listing above.
Learn more about the Pharma Inspection Line Lead – QC & cGMP role in the description above.
We appreciate your interest in this position.
Join Grand River Aseptic Manufacturing Inc. and contribute to our ongoing work.
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