CQV Engineer: GMP Validation & Commissioning
Listed on 2026-10-18
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Engineering
Validation Engineer, Pharma Engineer, Quality Engineering
Eurofins USA Bio Pharma Services in Edison, NJ is seeking a hands-on commissioning, qualification and validation engineer to join our CQV team. You will author and execute IQ/OQ/PQ protocols, perform field verifications against P&IDs and build toward owning qualification work streams.
This full-time role requires GMP experience, familiarity with 21 CFR Parts 210/211, and strong technical writing. You will collaborate with client engineering and quality teams on site, mentor newer engineers and
We are currently recruiting a CQV Engineer: GMP Validation & Commissioning for our team in Edison, NJ, United States.
The position is based in Edison, NJ, United States.
This opportunity is part of our work in Bio & Pharmacology & Health, Engineering.
The advertised compensation is 85..
We aim to respond to suitable candidates as soon as possible.
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