Overview:

• Total 7 years of experience in Testing services Automation Testing, Manual Testing, Regression Testing, Smoke Testing
• Good team player and quick learner with excellent technical and interpersonal skills.
• Expertise in Developing /Reviewing /maintaining the Test Plan, Test Cases Automated Test Scripts and manual , Test Results, Bug reports and Test Deliverables.
• in Agile and Waterfall with emphasis on Black box, Functional, GUI, System, regression, Smoke Test and Integration Testing of window based applications Client/Server Database Related Applications.
• Expertise good understanding of the Software Development Life Cycle SDLC
• Experience of Leading a team
• 3 years of experience in Automation and Agile methodology
• Having Good Experience in Industrial Automation and Health Care Clinical Domains
• Expertise in Electronic Data Capture EDC Product 'INFORM'

Technical Skills:

Professional Experience:

Confidential

Role: Team Lead

Confidential has features to add ability for Alarms in A2 to be shelved and update Alarm Manager to support Shelving. Leverage installations with AppServer Redundancy but support upgrade of redundant pairs one at a time, significantly reducing down time incurred by install. Adding feature to maintain similarities across all attributes ArchestrA IDE UI is simplified using View Model which is very user friendly and efficient to end user.

Responsibilities:

• Planning Sprint User Stories, attending Scrum meetings and validating Test deliverables
• Reviewing the Detailed Functional Specifications
• Identifying Test Scenarios and prepare Test Specification document
• Authoring, debugging, reviewing and executing Automation test scripts
• Raising Defects in Clear Quest, preparing Impact and Code Churn Analysis documents
• Perform Smoke test for Product builds, coordinating between Onsite and offshore team

Confidential

Role: Individual Contributor

This project is for the client that develops industrial automation software that delivers significant cost reductions associated with designing, building, deploying and maintaining secure and standardized applications for manufacturing and infrastructure operations..

Responsibilities:

• Attending Scrum meetings and validating Test deliverables
• Reviewing the Detailed Functional Specifications
• Identifying Test Scenarios and prepare Test Specification document
• Authoring, debugging, reviewing and executing Automation test scripts
• Raising Defects in Clear Quest, preparing Impact and Code Churn Analysis documents
• Perform Smoke test for Product builds, coordinating between Onsite and offshore team

Confidential

Role: Individual Contributor

Confidential project includes Application Server supports for Multi Galaxy Communication. As part of ArchestrA Baktun Project implementation includes ASB integration with Application Server, OPC Licensing, Security, Performance improvement etc. This Project is developed using Agile methodology.

Responsibilities:

• Attending Scrum meetings
• Reviewing the Detailed Functional Specifications
• Identifying Test Scenarios, authoring, debugging and executing Automation test scripts
• Raising Defects in Clear Quest, preparing Impact and Code Churn Analysis documents

Confidential

Role: Individual Contributor

Confidential is a platform-independent standard through which various kinds of systems and devices can communicate by sending Messages between Clients and Servers over various types of networks. It supports robust, secure communication that assures the identity of Clients and Servers and resists attacks.

Responsibilities:

• Attending Scrum meetings
• Reviewing the Detailed Functional Specifications
• Identifying Test Scenarios and prepare Test Specification document
• Authoring, debugging, reviewing and executing Automation test scripts
• Raising Defects in Clear Quest, preparing Impact and Code Churn Analysis documents

Confidential

Role: Team Lead

Confidential Pharmaceutical companies, medical device companies, and CROs to integrate and automate the management of their entire clinical development process. Phase forward is pioneer in EDC Electronic Data Capture called Inform, Clinical trial data management CDM tool called Clintrial and delivers the comprehensive clinical trial solutions needed to track product efficacy and safety from study initiation through FDA submission.

Responsibilities:

• Reviewing the Functional Specifications and prepare the Observations on it.
• Coordinating with onsite Development team to resolve defects
• Involved in Estimations
• Involved in the Preparation of Test plan, Test cases and review them
• Executed the test cases, documented test results and tracking defects
• Setting up the QA Environments, perform Smoke, Regression, Functional, Negative, Database testing and reporting defects
• Reviewed tasks done by Team members and prepare daily and weekly status reports

Confidential

Role: Individual Contributor

This Rules report shows the differences between Central designer template and study. The report consists of several columns like Rule name, Target Refname, Modified properties, Modifications, etc. For modified study rules, Modified Properties column in the report will be displayed all modified properties separated by semicolon. Values of these modified properties will be displayed in Modifications column separated by .

Responsibilities:

• Reviewing the Functional Specifications and prepare the Observations on it.
• Involved in the Preparation of Test plan, Test cases and review them
• Executed the test cases, documented test results and tracking defects

Confidential

Role: Individual Contributor

Confidential systems. At patient registration, a registration call is made for a patient where the Date of Birth, Sex will be provided to IVRS. The IVRS will generate the Patient ID.

Responsibilities:

• Reviewing the Functional Specifications and prepare the Observations on it.
• Involved in the Preparation of Test plan, Test cases and review them
• Executed the test cases, documented test results and tracking defects

Confidential This project emphasizes on managing the Clinical Trials. When the data points Mandatory patient details Ex: Screening Failure date, Withdrawal date etc. are inserted/updated in the Inform, an xml file will be generated. The xml file consists of the tags of all the data points but the data is generated only for inserted/updated data point.

Responsibilities:

• Reviewing the Functional Specifications and prepare the Observations on it.
• Involved in the Preparation of Test plan, Test cases and review them
• Executed the test cases, documented test results and tracking defects