Validation Specialist II: cGMP & ISO Compliance
Listed on 2026-10-18
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
bioMérieux, a leader in in vitro diagnostics, seeks a Validation Specialist II to develop and maintain comprehensive validation programs across equipment, processes and software. This role drives IQ/OQ/PQ activities, risk assessments, and documentation to sustain cGMP-compliant validated states within manufacturing and support operations.
The successful candidate will collaborate with Engineering, Manufacturing, QA/QC, and suppliers to ensure continuous improvement, audit readiness, and
We would love to welcome a new Validation Specialist II: cGMP & ISO Compliance to our group in Downers Grove, IL, United States.
The Validation Specialist II: cGMP & ISO Compliance role at bio Merieux is now open for applications in Downers Grove, IL, United States.
Join us at bio Merieux as our next Validation Specialist II: cGMP & ISO Compliance in Downers Grove, IL, United States.
We are currently recruiting a Validation Specialist II: cGMP & ISO Compliance for our team in Downers Grove, IL, United States.
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