About this opportunity
United Pharma lists this GMP CQV Validation Engineer for Site Startup opportunity in piscataway township, New Jersey. Review the employer’s description below for duties, qualifications and application requirements.
Job description
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.
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.