JOB DUTIES:
Sr. Software Engineer- Test/Verification/Validation for Medtronic, Inc. located at its facility in Mounds View, MN. Responsible for the design and implementation of software and web-based applications. Perform requirements gathering documentation, testing and maintenance of web application solutions. Perform Verification Test activities as part of the product lifecycle management for Cardiac Rhythm and Heart Failure (CRHF) and Medical navigation Software Products. Develop tests for custom medical device applications by creating test designs, analysis, test implementation and procedures for the verification of software requirements, documenting bugs, test case coordination. Develops FDA Class I & II & III Medical Device Software Applications and regulations that govern Medical Device Software such as IEC62304, CFR Part 820, 806 (Corrections & Removal). Responsible for the testing of instrument software for pacemakers, Implantable Cardioverter Defibrillators (ICDs), and Cardiac Resynchronization Therapy devices (CRTs). Responsible for the functional testing of software products including breaking down software requirement specifications to create strategic and efficient test plans. Utilizes Test and Defect tools to include Microsoft TFS (Team Foundation Server), Visual Studio or AzureDevops. Utilizes Software development with Test Automation and Frameworks. Leverages product software applications to include C#, .Net, VB (Visual Basic) Script, SQL and Java Script. Responsible for implementing Software Development Life Cycle (SDLC) with models to include Waterfall and Agile (SCRUM) and Software Testing Life Cycles (STLC). Coordinates requirements gathering documentation, testing and maintenance of web and mobile application solutions. Performs front end and back end web testing on Windows, Android, Linux and IOS operating systems. Utilizes MS Server technologies to include MS SQL and XML *multiple positions available.

REQUIREMENTS:
Bachelor' Degree or foreign equivalent in Information Technology, Computer Science, Computer Engineering or Software Engineering and 5 years' experience with software engineering; or alternatively a Masters' Degree or foreign equivalent in Information Technology, Computer Science, Computer Engineering or Software Engineering and 2 years' experience with software engineering. Experience must include one (1) year of post-bachelor's progressive experience in all the following: Verification of FDA class I & II & III Medical Device Software Applications that comply with IEC 62304, CFR Part 820; Testing of instrument software for pacemakers, Implantable Cardioverter Defibrillators (ICDs), and Cardiac Resynchronization Therapy devices (CRTs); Functional testing to include breaking down software requirement specifications for test plans; Test and Defect tools to include Microsoft TFS (Team Foundation Server), Visual Studio or AzureDevops; Software development with Test Automation and Frameworks; Product software applications to include C#, .Net, VB (Visual Basic) Script, SQL and Java Script; Software Development Life Cycle (SDLC) with models to include Waterfall and Agile (SCRUM) and Software Testing Life Cycles (STLC); Requirements gathering documentation, testing and maintenance of web or mobile application solutions; Front end and back end web testing on Windows, Android, Linux or IOS operating systems; MS Server technologies to include MS SQL and XML.

Additional Information

• Posting Date: Jan 18, 2022
• Travel: No