SRUTHI KAMBHAM adw4z7@r.postjobfree.com Mobile # 786-***-****

QA Analyst

Professional Experience

ISTQB certified and 12 Years of experience in Software Quality Assurance that includes manual and automated testing on Life Sciences Domain.

Self-motivated, proven and dedicated professional adept with managing software quality initiatives and influences development team to embed Quality in all phases of SDLC.

Expertise in Functional Testing, Black box testing, System Integration testing, data validation for migration projects, navigation testing, Smoke testing, GUI testing, Regression testing, Stress testing, Positive testing, Negative testing, Verification and Validation.

Created test plans, test cases and test metrics based on the requirements, design documents and Use Cases.

Extensive experience in review activities such as requirements, design, test scenario and test case

Proficient in the use of ALM/Quality Center (Test Director) for Web/J2EE based applications.

Experience in handling end to end deployments using JBoss and WebLogic Application servers and setting up the environment.

Knowledge in automation tools Selenium.

Proficient in defect tracking tools like Jira, Bugzilla and ALM for Test Case Management.

Efficient in testing MS SQL Server and Oracle database applications.

Have good exposure in performing Verification and Validation activities.

Experience in Testing both Agile/scrum and waterfall method.

Experience in Web services API testing using Soap UI and Postman.

Good experience and functional knowledge in regulatory domain

Improved product quality by developing Root Cause Resolution summaries for defects found during regression and for issues reported in production.

Strong communication and interpersonal skills.

Strong Team player and contribute towards the team goals. Ability to work productively and effectively in a team as well as individually.

Ability to handle multiple projects simultaneously.

Ability to multi-task while effectively managing time and meeting critical deadlines with little supervision.

Ability to coordinate activities in a fast-paced team environment.

Experience in handling regulatory product demos for various customers.

Professional Qualification

Bachelor of Technology from JNT University.

Certifications: ISTQB Certified Tester

Work Experience

ArisGlobal Software Pvt Ltd Mysore, India Aug’ 11 to Mar 2023

Title: QA Analyst

Projects Worked ON:

LifeSphere Regulatory Information Management System (LS RIMS)

LifeSphere RIMS is a comprehensive web application, which helps customers:

• Track, monitor, and control all the Registration related activities of the Medicinal Products.

• Comply with the regulatory procedures of different countries during the course of Products, Registrations.

• Customize the screens, fields, modules, and the user interface controls, to fulfil client business needs.

• To manage their data using Dashboards, Workflows, Alerts and Schedulers. LifeSphere RIMS is an end-to-end regulatory information management tool. It is also multi-tenant application which gives advantages of scalability and smooth upgrades.

Hands on Experience in handling the team of 5 to 10 people.

Ensured the information systems, projects met organization/industry quality standards and end-user requirements.

Developed quality standards through participating in the initial software development design stages.

Reviewed documents such as RD, Design Specifications & Data provided by the customers.

Prepared Test Estimation for Enhancements, Test Scenarios for the Projects.

Prepared and Reviewed the Test Cases in HP QC tool.

Responsible in performing the Sanity & Smoke on the builds provided and ensuring the released build.

Responsible for Test Execution of Integration, System Testing, Regression Testing.

Reporting software defects in a clear and concise manner and monitoring their progress till closure.

Preparing the Traceability Matrix, Test Summary Report, MOM`s.

Excellent exposure in providing the demo to the Customer on the project functionalities and have got multiple appreciations from the Managers.

Extensive Experience in handling the Customer Escalations & support to the customers.

Experience in Configuration Management tools like SVN and JIRA.

Actively participated in Scrum meetings, grooming sessions, and developed test scenarios.

Worked closely with BA, Developers and Business Users on critical issues, hot fixes and understand the requirements for applications.

Extensively used Jira for test planning, writing, uploading, and executing test Cases, bug tracking and reporting.

Highly involved in drafting test cases for different modules in application.

Responsible for Peer review for the Test Cases and Update based on the feedback, if necessary.

Performed Functional Testing, Integration Testing, Regression Testing and Back-end testing of the application manually.

Performed backend testing to validate database contents by writing and executing SQL Queries.

Actively participated in API Testing using POSTMAN that involves testing application programming interfaces (APIs) directly and as part of integration testing to determine if they meet expectations for functionality, reliability, performance, and security.

Conducted cross browsing testing in IE8, Mozilla, Chrome and safari using Browser stack.

Responsible for the raising defects in Jira and assigning them to concern developer or lead.

Involved in preparing Test Summary reports whenever necessary.

Responsible for doing testing on pre-production environment. Once deployment is done, responsible for doing post-production verification.

Involved troubleshooting production and non-production issues and performed root cause analysis.

Supported testing over the weekends to meet the deadlines for the releases.

Handled projects effectively, when there are no proper requirement documents and was able to quickly self-learn and provide test cases to third party team.

LifeSphere® Connect

The primary purpose of the LifeSphere® Connect integration solution is to help the pharmaceutical companies easily transfer the regulatory information data from other external applications (including Register) into agIDMP. The Regulatory information from any Regulatory Information Management System (RIMS) applications can be transferred to agIDMP through AMP XML. It has other features like:

• Mapping Controlled Vocabularies.

• Importing of xEVMPD CVs.

xEVMPD Submissions

The primary objective of xEVMPD submissions is to make the Medicinal Product information public in order to provide a complete list of all medicines authorized in the EEA. There are certain details such as excipients strength which are maintained confidential most of the times by the marketing authorization holders to avoid copy of the compositions by the competitors.

LifeSphere® EasyDocs

EasyDocs is a document management system which can be integrated with any web application.

• It can store the documents either in local or in any of the other DMS systems.

• It has all features of other DMS systems like checkout, check in, etc.

• It can easily connect with any other DMS systems.

Roles and Responsibilities:

Hands on Experience in handling the team of 5 to 10 people.

Ensured the information systems, projects met organization/industry quality standards and end-user requirements.

Developed quality standards through participating in the initial software development design stages.

Reviewed documents such as RD, Design Specifications & Data provided by the customers.

Prepared Test Estimation for Enhancements, Test Scenarios for the Projects; Prepared and Reviewed the Test Cases.

Responsible in performing the Sanity & Smoke on the builds provided and ensuring the released build.

Responsible for Test Execution of Integration, System Testing, Regression Testing.

Reporting software defects in a clear and concise manner and monitoring their progress till closure.

Preparing the Traceability Matrix, Test Summary Report, MOM`s.

Excellent exposure in providing the demo to the Customer on the project functionalities and have got multiple appreciations from the Managers.

Extensive Experience in handling the Customer Escalations & support to the customers.

REGISTER and RSM

The pharmaceutical companies throughout the globe use register product. Any product from the pharmacy company should register with the drug approval authority.

Key feature of a Register product enables to track, monitor, and control all the registration related activities of the products. Application helps the user to comply with the regulatory procedures of different countries during product registrations.

Creating the test environment and publishing the URL for the Testing.

Involved in TCD Drafting and TCD execution in various testing phases like Scope Testing, Functional Testing, Regression Testing, System Testing and Smoke Testing.

Worked in Beta and Alpha testing.

Identified and tracked defects using JIRA, Bugzilla.

Experience in Configuration Management tools like SVN.

Tracking the status of the reported bugs and updating the same as per the Process.

Conducting Walkthrough for the new requirements of the products/projects.

Demo on function requirements to the customers and other stakeholders of the project.

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