Experience may have been obtained concurrently and should includebr 3 yrs experience in quality management and process controlbr 3 yrs experience in Data Validation, including 3 yrs of experience in each of the following Data Migration Validation, Data Analysis and Data Verification using SQL queries for backendbr database tables, and File and Extract, Transform, Load ETL testing.br iii. 3 yrs Validation Life Cycle experience for customized internally developed systems for regulatory purposesbr 3 yrs experience with Implementing software projects in compliance with FDA 21 CFR Part 11 regulatory requirements and GAMP guidelinesbr 3 yrs experience creating and updating UFRSbr 3 yrs experience preparing Validation Plansbr 3 yrs experience preparing RAbr 3 yrs experience performing system testing, system integration testing and regression testingbr 3 yrs experience creating and maintaining TMbr 3 yrs experience developing, coordinating and executing IQ protocols, OQ, PQ protocolsbr 3 yrs experience providing quality direction and review of the protocolsbr 3 yrs experience identifying and resolve any deviations including implementation of any required CAPAsbr 3 yrs experience creating Validation Final Reportsbr 1 yr experience with HP ALMbr Must have legal authority to work in U.S
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