GMP CQV Validation Engineer Site Startup
Listed on 2026-10-13
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Pharmaceutical
Pharma Engineer, Validation Engineer
United Pharma in Piscataway, NJ, seeks a Validation Specialist to support qualification activities for manufacturing equipment, facilities, and utilities during a high-priority site startup. You will draft and execute FAT/IQ/OQ/PQ protocols and partner with Maintenance, Engineering, Quality, and external vendors.
The role requires 2+ years in a cGMP environment, knowledge of GDP and FDA regulations, and the ability to manage schedules and generate progress reports. Weekend hours may be required.
This opening is for the GMP CQV Validation Engineer for Site Startup role at United Pharma.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Piscataway Township, NJ, United States.
This opportunity is part of our work in Bio & Pharmacology & Health, Engineering.
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