NEED IMMEDIATE JOINERS
Pharmacuetical/CRO industry experience is required for this role!
- 21 CFR Part 11, EU Annex 11, GAMP5, GxP and CSV guidelines that are applicable to Life sciences/Pharma industry,
- Performance testing, security testing, negative testing
- SDLC and Validation deliverables like URS, FRS, Configuration specifications, Test Plan, Test Summary report, Validation Plan, Validation Summary report documents.
- Test Scenarios, Test Cases/Scripts, Requirement Traceability Matrix(RTM), IQs (Installation Qualification) Scripts, OQs (Operational Qualification) Scripts, UAT/PQs(Performance Qualification/User Acceptance Testing) scripts .
