CQV Engineer: Pharma Validation & Commissioning
Listed on 2026-09-25
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Engineering
Pharma Engineer, Validation Engineer, Biomedical Engineer, Quality Engineering
GxP Associates in New Jersey seeks a motivated CQV Engineer with 0-3 years to support Commissioning, Qualification, and Validation activities across regulated life-sciences facilities. You will gain hands-on exposure to IQ/OQ/PQ execution, equipment and system qualification, and documentation.
You will collaborate with Engineering, Validation, Quality, Manufacturing, and Project teams to ensure systems are properly commissioned and compliant with cGMP.
The CQV Engineer:
Pharma Validation & Commissioning role at GxP Associates is now open for applications in NJ, United States.
Join us at GxP Associates as our next CQV Engineer:
Pharma Validation & Commissioning in NJ, United States.
We are currently recruiting a CQV Engineer:
Pharma Validation & Commissioning for our team in NJ, United States.
This is a great opening to take on the CQV Engineer:
Pharma Validation & Commissioning role at GxP Associates.
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