Pharma Validation Engineer — GMP & CPV Expert
Listed on 2026-10-15
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Engineering
Pharma Engineer, Biomedical Engineer, Quality Engineering -
Quality Assurance - QA/QC
Quality Engineering
Serovia in New Jersey is seeking a Validation Engineer to execute and maintain site validation activities across equipment, processes, and systems, ensuring cGMP compliance and a qualified state throughout the product lifecycle.
You will collaborate with Manufacturing, Engineering, QA, and Regulatory Affairs to execute PPQ/PQ/CPV, develop validation documents, and support regulatory inspections; strong writing and risk-analysis skills are required.
This opportunity is for the Pharma Validation Engineer — GMP & CPV Expert role at Serovia.
The following opening is for a Pharma Validation Engineer — GMP & CPV Expert with Serovia.
Our organisation is growing, and we are hiring a Pharma Validation Engineer — GMP & CPV Expert in Branchburg Township, NJ, United States.
This opening is for the Pharma Validation Engineer — GMP & CPV Expert role at Serovia.
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