Professional experience in Validation Practices with a good understanding of GxP (GMP, GLP, GAMP) standards and 21 CFR Part 11 and EU Annex 11 Guideline.Strong experience in development of Validation Protocols like Functional Risk Assessments, Installation Qualification, Operational Qualification ,Performance Qualification , Tractability Matrix , Validation Summary Report for the related applications.experience in writing Test procedure Test Cases, Test Scripts and Test Result.Experience in preparation of Validation Master Plan and Risk Assessment Plan. Experience in System Assessment against compliance requirements based on GAMP 5 Computerized System Validation practices as well as regulatory requirement.Specialties: PLC/ SCADA Validation, Pharmaceutical Validation, Software System Validation (Laboratory based Software/ Clinical Trial Management Software, SAP), Computer System Validation, , ERP Validation , Excel sheet Validation, SAP Validation.