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VALIDATION ENGINEERS
VALIDATION ENGINEERS-November 2024
South Plainfield
Nov 22, 2025
About VALIDATION ENGINEERS

　　Review and approve of all Validation Protocols. Perform IQ/OQ/PQ, and process validation for laboratory analytical equipment. Conduct Gap analysis and Remediation procedures according to 21 CFR Part 11 Compliance and prepare deviation reports. Review and revise system related SOP's (Standard Operating Procedures), WO's (Work Orders), QOPs (Quality Operating Procedures), and all other department standards and compliance documentation as applicable. Review validation plans, draft, and review validation reports, and traceability Matrix. Master’s degree in Science, Technology, or Engineering (any) is required. Work location: South Plainfield, NJ and various unanticipated locations throughout the U.S.Send Resume to HR Dept., United Pharma Technologies, Inc., 908 Oak Tree Avenue, Suite A, South Plainfield, NJ 07080.

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