Divya P

Quality Assurance Specialist - 7 Years of Experience - Near 75093


Quality Assurance Specialist


Plano, TX

Education Level:


Will Relocate:



Professional SUMMARY * Over all 7 years of experience in the IT industry in Quality Assurance using Web based and Client/Server applications. * Knowledge of Healthcare, Pharma, Security and Biometric projects. * Key expertise includes testing Extensive experience in Manual and Automated testing using Selenium and defect tracking tools like HP Quality Center (ALM/QC), Bugzilla, JIRA and Bug Zero. * Conversant with all phases of Project Life Cycle including Requirement gathering, Analysis, Design, Development, Testing and Implementation of Quality Software. Experienced with all phases of Software Development Life Cycle (SDLC) and Software Testing Life Cycle (STLC) using various module like Waterfall and Agile/Scrum. * Proficient in analyzing system requirements, use cases and other documents to gain overall understanding of the new application to determine the appropriate level of testing required and creating Test Plans and Test Cases, Test Scripts, Requirement Traceability Matrix (RTM), Test Environments and analyzing Test Results based on requirements. * Good experience in performing Verification and Validation activities which includes preparation of test scripts, step -by-step execution, consolidation and reporting bugs & defects. * Experience in writing and executing SQL queries to perform back-end testing for data integration and validation. * Good exposure to Web technologies like HTML, XML and JavaScript. * Expertise in Manual Testing for Web and Client/Server applications on UNIX and Windows Platforms. * Proficient in Integration Testing, System Testing, GUI Testing, Stress Testing, Backend Testing, Black box Testing and Functional Testing * Coordinated with Onsite/Offshore resources to fix Quality Center queries during SIT and UAT. * Proven ability to work efficiently in both independent and team work environments. * Experience in IVR/IWRS Testing. * Knowledge of clinical data management process for FDA regulated companies is a plus. Familiarity with FDA regulations such as 21 CFR Part 11 and GxP desirable * Communicating with internal clients in stand up calls for new Project kick off, update on the health of the project for potential risks & suggestions on risk mitigation during testing and been part of UAT SETUP & participation. * Part of Client Audit by PRA, Takeda, Sanofi Pastuer, Pfizer, Roche, Merck-Sereno, AstraZeneca, Novo-Nordisk, Novartis, J&J, ALG * Enthusiastic and passionate in learning new technologies and architectures. Good listener with strong problem solving, analytical and logical skills. 5 Years of Experience from PAREXEL international Ltd * 1.5+ Years of Experience from CMC Ltd