CQV Engineer: GMP Validation, Commissioning Utilities
Listed on 2026-10-17
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Engineering
Pharma Engineer, Validation Engineer, Quality Engineering, Biomedical Engineer
Eurofins Scientific is seeking a hands-on CQV Engineer to join our team in Edison, NJ. You will work with the CQV Lead on facility, utility and equipment qualification programs, authoring IQ/OQ/PQ protocols, performing field walkdowns, and maintaining rigorous documentation for GMP-compliant projects.
Ideal candidates have 2+ years in GMP-regulated environments, reading P&, strong technical writing, and a willingness to grow into leading qualification work streams.
The CQV Engineer: GMP Validation, Commissioning, & Utilities position in the Bio & Pharmacology & Health, Engineering field is open for applications.
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 Validation, Commissioning, & Utilities role in the description above.
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