About this opportunity
Serovia lists this Pharma Validation Engineer — GMP & CPV Expert opportunity in branchburg township, New Jersey. Review the employer’s description below for duties, qualifications and application requirements.
Job description
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.
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.