CQV Engineer: GMP Qualification & Validation Lead
Listed on 2026-10-17
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Engineering
Pharma Engineer, Quality Engineering, Biomedical Engineer -
Quality Assurance - QA/QC
Quality Engineering
Eurofins is seeking a hands-on CQV Engineer to support commissioning, qualification and validation for pharmaceutical and biotech facilities. You will author and execute IQ, OQ and PQ protocols, perform field verifications, and drive deviations and investigations in a GMP-regulated environment.
The role requires 2+ years GMP experience, ability to read P&IDs, strong technical writing, and willingness to work on site in Raleigh, NC with standard hours and occasional overtime; benefits include
Are you ready to take on the CQV Engineer: GMP Qualification & Validation Lead role at Eurofins?
As a CQV Engineer: GMP Qualification & Validation Lead, you will play an important part at Eurofins in Raleigh, NC, United States.
We invite applications for the CQV Engineer: GMP Qualification & Validation Lead position located in Raleigh, NC, United States.
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