Pharma Validation Analyst
Company: Vforce Infotech
Location: New Brunswick
Posted on: May 7, 2022
Job DescriptionThe Validation Analyst is responsible for
validating computerized systems used for electronic data and
records that support regulatory submissions or are subject to
regulatory inspection. Primary responsibilities include Validation
Planning, Installation Qualification (IQ), Operational
Qualification (OQ) and Performance Qualification (PQ) of
computerized systems.Duties Include:
Creation/Review/Modification/execution of validation plans. Review
of User Requirements Specifications (URS), Functional Requirements
Specifications (FRS) and Detailed Design Specifications for
conformance to industry standards. Creation/Review/Modification of
IQ, OQ and PQ test protocols. Execution of test scripts for IQ, OQ,
and PQ. Test deviation reporting and resolution.
Creation/Review/Modification of the Traceability Matrix for tracing
requirements to testing. Creation/Review/Modification of Validation
Summary Reports. Perform Gap Analysis and Retrospective Systems
Validation. Review validation documentation for accuracy and
compliance with company procedures.
Keywords: Vforce Infotech, New Brunswick , Pharma Validation Analyst, Professions , New Brunswick, New Jersey
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