Senior CQV Engineer — GMP Validation & Commissioning
Listed on 2026-11-04
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Engineering
Validation Engineer, Pharma Engineer, Quality Engineering, Biomedical Engineer
Adryan is seeking a hands-on commissioning, qualification and validation (CQV) engineer for life sciences projects in the United States. You will manage CQV activities for GMP facilities, equipment, and utilities, ensuring compliance with FDA/EU guidelines and quality standards.
You will design, execute, and document IQ/OQ/PQ processes and generate final reports.
Required:
Bachelor’s in engineering or related field, 5+ years GMP, 3+ years CQV, and strong teamwork, communication, and
This is a strong position to take on the Senior CQV Engineer — GMP Validation & Commissioning role at Adryan.
Consider building your career as a Senior CQV Engineer — GMP Validation & Commissioning at Adryan.
The Senior CQV Engineer — GMP Validation & Commissioning position in the IT & Technology field is open for applications.
We have an opening for a Senior CQV Engineer — GMP Validation & Commissioning in Iowa, LA, United States within IT & Technology.
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