Senior CQV Engineer — GMP Validation & Commissioning
Listed on 2026-10-06
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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
Our organisation is growing, and we are hiring a Senior CQV Engineer — GMP Validation & Commissioning in Iowa, LA, United States.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Senior CQV Engineer — GMP Validation & Commissioning role in the description above.
We appreciate your interest in this position.
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