CQV Engineer: GMP‑Driven Commissioning & Validation
Listed on 2026-10-18
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Engineering
Validation Engineer, Pharma Engineer
Eurofins USA Bio Pharma Services in Raleigh, NC seeks a hands‑on CQV engineer to lead commissioning, qualification and validation activities for pharmaceutical and biotech clients. You will author and execute IQ/OQ/PQ protocols, perform field verifications, and manage documentation throughout qualification campaigns.
Ideal candidates have GMP experience, are comfortable working on active sites, and can develop end‑to‑end qualification work streams while mentoring junior engineers.
We invite applications for the CQV Engineer: GMP‑Driven Commissioning & Validation position located in Raleigh, NC, United States.
The position is based in Raleigh, NC, United States.
This opportunity is part of our work in Engineering.
The advertised compensation is 85..
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 CQV Engineer: GMP‑Driven Commissioning & Validation role in the description above.
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