CQV Engineer: GMP Validation & Qualification Pro
Listed on 2026-10-18
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Engineering
Pharma Engineer, Biomedical Engineer, Quality Engineering -
Quality Assurance - QA/QC
Quality Engineering
Eurofins USA Bio Pharma Services is seeking a Commissioning, Qualification, and Validation (CQV) Engineer to join our Boston area team. You will author and execute IQ/OQ/PQ protocols for utilities, equipment, and facilities, and perform field verifications against P&IDs.
You will collaborate with client engineers and quality groups, grow into owning end-to-end qualification work streams, and travel as needed to support campaigns on site in GMP environments.
We are looking to fill the CQV Engineer: GMP Validation & Qualification Pro position at Eurofins USA Bio Pharma Services in Boston, MA, United States.
This posting is for the CQV Engineer: GMP Validation & Qualification Pro role at Eurofins USA Bio Pharma Services, based in Boston, MA, United States.
The CQV Engineer: GMP Validation & Qualification Pro role at Eurofins USA Bio Pharma Services is now open for applications in Boston, MA, United States.
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