Validation Specialist II — cGMP Compliance & Validation
Listed on 2026-10-18
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
bioMérieux seeks a Validation Specialist II to develop and maintain validation programs ensuring compliant processes, equipment, software, and environments in our Illinois manufacturing operations. You will plan, execute, and lead validation activities while supporting continuous improvement and cross‑functional collaboration.
The role requires a Bachelor's in a related field and at least two years of cGMP validation experience, with strong documentation and problem‑solving skills.
Join us at bio Merieux as our next Validation Specialist II — cGMP Compliance & Validation in Des Plaines, IL, United States.
We are currently recruiting a Validation Specialist II — cGMP Compliance & Validation for our team in Des Plaines, IL, United States.
This is a genuine position to take on the Validation Specialist II — cGMP Compliance & Validation role at bio Merieux.
As a Validation Specialist II — cGMP Compliance & Validation, you will play an important part at bio Merieux in Des Plaines, IL, United States.
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