Quality Analyst
Resume:
Deepalakshmi Seshachalam Visa Type: EAD
Mobile: 856-***-**** Email: ************.***********@*****.***
SUMMARY
Around 5 years of experience as Quality Analyst(Validation Analyst) in Cognizant Technology Solutions (CTS) in Life Science Domain and have exposure to SDLC & Testing Methodologies to certify the Web based Applications
Certified tester in ISTQB (CTFL)
Very Good Exposure in Manual Software Testing, Life Science Validation Testing, Security Testing, Interface Testing, System Integration Testing (SIT), End to End Testing, Regression Testing, UAT Testing, Internet Upgrade Testing, Compatibility Testing and IVRS testing, Web Service testing
Involved in different Phases of software testing like Requirement analysis, Estimation, Test Strategy preparation & Planning, Test Design, Test case Scripting, Test Data Preparation, Test Execution, Defect Management(Defect Reporting/ Tracking /Closure), RTM preparation and Good Documentation Practices (GDP)
Exposure to Waterfall Model and Agile Model
Very good exposure in ALM(QC), JIRA, Oracle SIEBEL, SQL, Share Point UI
Exposure in Soap UI, Selenium IDE and Selenium Web Driver, mobile testing
Experience in automating regression test case using selenium with java
Intensive communication with both on-site and offshore Developers (In-house and Third Party), Business Analysts, Project Managers, Test Team, business SME etc.
Extensive experience working with several downstream
Allocation of workload to team members to meet test deadlines in the most efficient manner
Progress reporting, Completion reports, Mentoring/training new recruits/juniors.
Had conducted training sessions on Validation concepts, Quality Center, Oracle SIEBEL and also conducted Internal QA audits.
Had coordinated and participated Delivery Assurance/Quality Assurance audits.
Very good exposure on C20 – Project Management Tool to track the project and collect metrics.
AREAS OF EXPERTISE -- Technical
Domain Knowledge
Life Sciences
Project Management Tool/IDE’s
Mercury Quality Center(ALM),Share Point UI, C20
Defect Management Tool
JIRA, Mercury Quality Center(ALM)
Technology
Oracle (SIEBEL e-Clinical), Selenium IDE and selenium Web Driver
Project Methodology
Waterfall, Agile
Others
Java Basics, Soap UI, XML Wrench, MS Office(MS Word, MS Excel, MS Outlook, Visio)
EDUCATIONAL QUALIFICATION
Title of the Degree with Branch
College/University
Year of Passing
B. Tech (Biotechnology)
SRM University
2008
CERTIFICATIONS/TRAININGS
External Certifications,
ISTQB – Foundation Level (International Software Testing Qualification Board Certification)
Cognizant Certified Professional in,
Software Testing (L0)
Validation Testing (L1)
Life Sciences Testing (L0)
Life Sciences (L0)
KEY PROJECT PROFILES
Project #1:
EPIC Duration : Jan 2013 to Aug 2013
Abstract
The EPIC system manages and controls documents from many different business disciplines within Research and Development of the client. The intended audience includes the key business stakeholders and their management, as well as the Enterprise Content Management Core and Architecture teams.
Roles and Responsibilities
Played as Team lead for offshore 4 members team to ensure quality deliverable on time
Perform Static Testing of Requirement specification and Test script
Supported quality and compliance assessment
Perform Static Testing of Requirement specification and Test script
Involved in phases like Test Estimation, Test, Strategy documentation, Test script preparation, RTM, Test Execution, Defect management, Test Closure
Used Selenium IDE for web testing
Involved in automating regression test cases using selenium web driver with java
Involved in Status Reporting to leadership team
Provided Regulated system validation guidance
Involved in Process related activities line C20 and metrics data collection
Involved in Project specific KT document preparation
Project #2:
VACSI Duration : Aug 2011 to Dec 2012
Abstract
VACSI is a system that enables external vendors to enter subject enrolment information into Amgen’s
Clinical Trial Management system. The interface is a unidirectional data push from the vendor to the
Amgen CTMS and should be accessible to current and future vendors.
VACSI is separated into two components, Biz Talk and CTMS. Biz Talk receives messages from
the external vendor and performs some basic logic. Biz Talk then calls the CTMS component
where the CTMS imports subject data contained in the message. Errors during this process that
are identified by Biz Talk or the CTMS are reported via the Biz Talk component.
Roles and Responsibilities
Played as Team lead for offshore 4 members team to ensure quality deliverable on time
Perform Static Testing of Requirement specification and Test script
Supported quality and compliance assessment
Perform Static Testing of Requirement specification and Test script
Involved in phases like Test Estimation, Test, Strategy documentation, Test script preparation, RTM, Test Execution, Defect management, Test Closure
Involved in Status Reporting to leadership team
Provided Regulated system validation guidance
Involved in Process related activities line C20 and metrics data collection
Involved in Project specific KT document preparation
Project #3:
eClinical Duration : Nov 2009 to Nov 2013
Abstract
eClinical is used to perform, manage, track and provide reporting on information for clinical studies. The
system is a Commercial off the Shelf (COTS) software package manufactured by Oracle Corporation.
The software is based on Siebel technology. The system provides functionality to support the clinical
development activities across many functions.
Roles and Responsibilities
Played as Team lead for offshore 4 members team to ensure quality deliverable on time
Perform Static Testing of Requirement specification and Test script
Supported quality and compliance assessment
Perform Static Testing of Requirement specification and Test script
Involved in phases like Test Estimation, Test, Strategy documentation, Test script preparation, RTM, Test Execution, Defect management, Test Closure
Involved in Status Reporting to leadership team
Provided Regulated system validation guidance
Involved in Process related activities line C20 and metrics data collection
Involved in Project specific KT document preparation
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