QMS Software
This software have multiple modules to Events, Document control, Equipment, CAPA, Change control to handle various QMS workflow. I worked as tester to create Test Plan, Test Script, test Evidences using JIRA.
Tentang Saya
Computer System Validation/MES(Syncade) Validation/Regulatory Compliance(FDA) GAMP5,21CFR Part 11/QMS/GMP/LifeScience Extensive Experience on Testing methodologies like Usability Testing/User Interface Web Based Application Testing Desktop Application Testing Integration Testing, Regression Testing,Installation Testing Mobile Apps Testing Performance/Penetration Testing Cross browser Testing MES Validation Medical Device Testing Documentation on Validation-Project and Quality Exécutions Plan, Engineering Plan, Validation Project Plan, Traceability Matrix, Configuration Management Plan, Design Review Procedure, DCC, DRI, Configuration Item List, Functional Risk Assessment, Code Review Plan, Code Review Report , Software Factory Acceptance Test, User Acceptance Test, Validation Protocol Installation Qualification/ Operational Qualification documentation, Periodic Review Report, Standard Operating Procedures, Design Review Report and Validation Summary Report according to 21 CFR Part 11 and FDA regulations for the
$17 USD/jam
PEKERJA BEBAS BARU
