Dynamic, Results-driven, dedicated professional with good experience in the software test engineering industry. A methodical and a resourceful engineer who obtained quality assurance and testing experience while working for an electronic health record (EHR) provider software company. Rich experience in compliance to government regulations, industry standards and quality system regulations

• Software Quality Assurance and Application development life cycle experience with key projects ranging from Cerner implementation in health care industry for Electronic medical records, Medical device manufacturer and Insurance billing.
• 4 years of experience in Software Test design, Testing and Quality Assurance Management.
• In-depth knowledge of Software Development Life Cycle(SDLC) , Software Testing Life Cycle, Defect Life Cycle and different types of testing.
• Experienced in Functional Testing, Integration testing, System and User acceptance testing.
• Experienced in Analyzing Use cases /Functional specification documents, create functional test cases and Traceability Matrix to ensure test coverage.
• Integrated knowledge of end to end workflows from ADT, ASAP, Orders (CPOE), Clinical Documentation to Insurance claims and Guarantor statements.
• Experienced to work with both waterfall and Agile Methodologies.
• Experienced in the use of agile approaches, including Test-Driven Development and Scrum.
• Experience in testing different security user roles in EHR implementations.
• Experienced in FDA Quality systems regulations (QSR). Experienced in verification and validation following QSR and procedures following 21 CFR 820 guidelines.
• Experience in working with developers, testers and business users from onsite and offshore
• Experience working on Quality Assurance tools – HP Quality center 10.0.
• Quality Assurance documents - Master Test Plan, Test cases, end to end clinical and financial work flows ,Test scenarios, Requirements traceability to test cases, Test summary report after evaluating entry and exit criteria and test defect management.
• Good overview over Databases such as MS Access, MS SQL Server and Oracle.
• Ability to work and build strong professional relationship with product management teams, Software application development teams, Environment teams and with different business clients.

Professional Experience:

QA/ Test Analyst, Kansas City, MO
Confidential Feb 2009 –Present

Confidential is an Enterprise Healthcare management system includes Cerner Clinicals, Cerner Financials, Cerner Cardiology, and Cerner Scheduling etc. It is a health information solution that synchronizes workflow across the entire enterprise. It orchestrates patient care by bringing together clinical, financial, therapeutic and diagnostic information.

Job Responsibilities:

• As a scrum QA testing team member coordinated and worked with the business SME’s, R&D development team members.
• Tested different Cerner functional components, Involved in different phases of testing like Functional testing, Integration testing, System testing and User Acceptance testing or Beta testing.
• Cerner Financials deals with Patient Access, Revenue Management, Guarantor billing, Claims processing and Reporting. Tested different electronic and paper based claims.
• Cerner interoperates between multiple applications and transmits data through interface engine, open link to different health care external systems and insurance payers. Involved with Interface team and validated HL7 events and messages.
• Cerner Clinical Access embodies Best Practice Integration capability by delivering electronic patient information to medical imaging modalities. Tested radiology work flows and validated with different external systems like PACS using DICOM.
• Cerner contributes to HIPAA compliance, especially with regard to security of patient information
• Documenting Master Test Plans. Reviewing Test plans
• Contributed extensively towards Manual testing, Web based testing and Client/Server testing.
• Knowledge about Traceability matrix.
• Identifying and adapting the existing general system standards, rules of system testing and communicating QA guidelines and standards to the development and business teams.
• Involved in identifying key end to end System test work flows.

Environment: Java, J2EE, PL/SQL, Google Web Toolkit (GWT), QTP, XML, Microsoft Visual Studio,
Test Tool – HP Quality center 10.0

QA Analyst

Confidential, powered by the Siemens REMIND (Reliable Extraction and Meaningful Inference from Non-structured Data) platform, replaces manual chart reviews with automated chart abstraction of quality measures. Siemens Device Connect enables electronic collection of information from GE Healthcare’s DINAMAP vital signs monitors.
Siemens Device Connect helps healthcare providers achieve clinical automation, error reduction, and cost control with innovative workflow technology .Using an automated approach to the patient vitals collection process. It enables electronic collection of information directly from vital sign monitors, streamlining the tasks of identifying patients, recording observations, and validating the documented vital signs.

• Direct capture of vital signs information without transcription
• Transmits validated data through standard HL7 interface
• Displays comprehensive non-invasive vital signs – blood pressure, pulse, oxygenation
• Reduce delays in care due to waiting for vitals data transcription
• Increase nursing productivity by eliminating process steps
• Improve patient safety by eliminating opportunity for transcription error
• Sends data to the clinical repository for access from practically anywhere in the enterprise
• Overcomes the limitations of manual, paper-based vitals collection
• Increases patient safety by avoiding opportunities for transcription errors

Job Responsibilities:

• Understood business requirements, software design and tested end to end work flows by developing in-depth integration Test suites within Quality Center
• Tested the clinical data that interfacing between GE DINAMAP and Siemens Clinical application in compliance with FDA regulations.
• Experienced in FDA Quality systems regulations (QSR). Involved in verification and validation following QSR and procedures following 21 CFR 820 guidelines.
• Involved in 820. 30g Design Validation and Validation Documentation.
• Involved in 820.60 in identification and traceability of procedures and requirements.
• Conducted backend tests by writing SQL queries for database verification to access and setup test data
• Developed defect management workflows, test reporting metrics.
• Involved in Functional testing, Integration testing, System testing, Interface testing and user acceptance testing by interacting with end users.

Environment: PL/SQL, Rational Clear Case, Rational Clear Quest, Visio 2000, XML, Microsoft Visual Studio, Visio, Snag It