CQV Engineer – GMP Validation & Commissioning
Listed on 2026-10-18
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Engineering
Pharma Engineer, Validation Engineer, Biomedical Engineer -
Pharmaceutical
Pharma Engineer, Validation Engineer
Eurofins USA Bio Pharma Services in Edison, NJ, is hiring a CQV Engineer to lead commissioning, qualification and validation activities for pharmaceutical facilities. This full‑time role involves writing and executing IQ/OQ/PQ protocols, performing field walkdowns, and documenting results in support of FDA‑readiness.
You will work with client engineering and quality teams, grow toward owning systems end to end, mentor newer engineers, and contribute to risk assessments and change control while
Are you ready to take on the CQV Engineer – GMP Validation & Commissioning role at Eurofins USA Bio Pharma Services?
This opening is for the CQV Engineer – GMP Validation & Commissioning role at Eurofins USA Bio Pharma Services.
We are seeking a motivated CQV Engineer – GMP Validation & Commissioning to join Eurofins USA Bio Pharma Services in Edison, NJ, United States.
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