CQV Engineer: GMP-Driven Commissioning & Qualification
Listed on 2026-10-17
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Engineering
Pharma Engineer, Validation Engineer, Biomedical Engineer
Eurofins USA Bio Pharma Services seeks a hands-on CQV professional for commissioning, qualification and validation in pharmaceutical/biotechnology settings in the Boston area. You will write and execute IQ/OQ/PQ for utilities, equipment and facilities, and collaborate with engineering and QA teams to deliver compliant qualification programs.
Applicants should have 2+ years in a GMP-regulated environment, read P&IDs, and demonstrate strong technical writing.
We have an opening for a CQV Engineer: GMP-Driven Commissioning & Qualification in Boston, MA, United States within Bio & Pharmacology & Health, Engineering.
Take a moment to read everything above and see whether this role is right for you.
This posting is for the CQV Engineer: GMP-Driven Commissioning & Qualification role at Eurofins Bio Pharma Product Testing North America, based in Boston, MA, United States.
We are looking to fill the CQV Engineer: GMP-Driven Commissioning & Qualification position at Eurofins Bio Pharma Product Testing North America in Boston, MA, United States.
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