Experience in Software Quality Assurance, Business Analysis, Validation and Testing in Life science/Pharma domain. · 5 years of experience in QA/Project Management · 2+ years of Onsite implementation consultant experience from February 2007 to April 2008 and March 2012 to November 2012 (EVMPD implementation).· Experience with different software life cycle methodologies. Extensively used agile development methodology (Scrum and Kanban). Played role of Scrum master.· Experience in Requirements Gathering & Analysis.· Experience in creating the Validation Protocols FRS, URS, RTM, IQ, OQ, PQ, SOPs, Test Plans, Test Scripts and VSRs.· Good working experience in FDA regulated environment including 21CFR part11, GCP, GMP and ICH guidelines including detailed understanding of Regulatory requirements and guidelines.· Experience in Functional and Non-functional testing of Cloud based web applications.· Experience with REST APIs testing· Experience in analyzing data and utilize SQL queries in Oracle to validate data.· Open for an Individual Contributor role.Reponsibilities:Lead, Manage and Drive QA teams in agile methodology on multiple products development. · Negotiate, plan and manage all release activities.· Involved in preparation of Test scenarios, test cases referring to specification documents for different types of testing.· Complete responsibility of all QA deliverables and Change Management.· Arrange and conduct review, bug triage, Sprint retrospective and CCB meetings.· Involved in preparation & review of test plan, Release Notes, IQ, OQ, PQ and Test/Validation summary report.· Training to QA team on new technologies and tools.· Client interaction and issue escalation.· Involved in testing applications for Mobile support.· Involved in identifying scenarios to be automated and ensure it is automated successfully