Validation Specialist II – GMP & Compliance Lead
Listed on 2026-10-18
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
bioMérieux is seeking a Validation Specialist II in Illinois to develop, implement, and maintain validation programs across equipment, processes, software, and cleaning systems. The role plans and executes validation activities and collaborates with cross-functional teams to uphold validated states.
Responsibilities include creating protocols and reports, handling deviations, and supporting audits while ensuring compliance with cGMP, ISO 13485, FDA 21 CFR Part 11, and GAMP guidelines.
This posting is for the Validation Specialist II – GMP & Compliance Lead role at bio Merieux, based in Lyons, IL, United States.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Lyons, IL, United States.
This opportunity is part of our work in Bio & Pharmacology & Health, Engineering.
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