Inspire Medical Systems, Inc.
Software Verification Engineer
Inspire Medical Systems, Inc., Golden Valley, Minnesota, United States,
Software Verification Engineer - Minneapolis, MNABOUT INSPIRE MEDICAL SYSTEMSInspire is the first of its kind medical device designed to make a difference in the lives of those living with Obstructive Sleep Apnea (OSA). We are revolutionizing the sleep industry with our FDA-approved medical device, designed to reduce OSA severity for those who cannot tolerate or get consistent benefit from CPAP. Our focus on patient outcomes is at the core of everything we do, and our "think I can" attitude drives us to make a difference in the lives of those seeking alternative sleep apnea treatments.WHY JOIN OUR FAST-GROWING TEAMAt Inspire, we value people - your diverse experiences, backgrounds, and thoughts. We elevate voices and encourage learning opportunities to build a professional network that grows into community. We embrace a people-first culture by offering hybrid work schedules, excellent benefits, 401k matching, ESPP, flexible time off (FTO), and tuition reimbursement.If you're passionate about making a difference in people's lives and want to work with innovative technology, come be a part of our great team!ABOUT THIS POSITIONWe are recruiting for a Software Verification Engineer to join our team. You will be responsible for the requirements analysis, test design, test automation, execution, and verification of embedded software. You will work cross-functionally with other team members on testing and verification deliverables supporting multiple software development initiatives.OPPORTUNITIES YOU WILL HAVE IN THIS ROLEAnalyze System and Software requirements to determine testability, completeness and consistency.Perform ripple effect analysis for requirements and design level changes using technical standards, principles, theories, concepts and techniques as they relate to software testing.Help Agile teams achieve Definition of Done (DoD) for software development with focus on testing and test automation deliverables, such as:
Developing test protocols by performing in-depth requirements analysis.Compiling data and defining changes required in testing equipment, testing procedures, or new testing requirements.Executing automated and manual test protocols following established procedures and capturing appropriate objective evidence.Coaching assigned cross-functional team contacts on testing processes, tools, and best practices.
Report and investigate observations and defects, working with other members of the development team to establish root cause and options for correction.Provide and manage traceability evidence between requirements, tests and risk documentation.Write formal test plans and reports that can be used in submission packages to regulatory agencies.Generate and approve design history file documents, device master record documents, engineering change order records, and other quality system documents and records as assigned.Develop, disclose, and support the patenting of innovative technology and solutions.WHAT YOU CAN BRING TO OUR GREAT TEAMRequired:Bachelor's Degree in Engineering, Software, Computer Science, or related discipline or equivalent experience2+ years of similar experience, including software testing, test automation, verification experience and/or software development experience.Strong written and verbal communication skills with the ability to communicate with both internal and external stakeholders and senior leadership.Proficient with MS Office Suite (e.g., Word, Excel, Outlook, etc.)Preferred:Advanced level degree in Engineering, Software, Computer Science, or related disciplineClass III medical device experiencePrevious experience developing and/or testing embedded software architectures.Additional development experience utilizing .NET, C#, and/or C++.
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Developing test protocols by performing in-depth requirements analysis.Compiling data and defining changes required in testing equipment, testing procedures, or new testing requirements.Executing automated and manual test protocols following established procedures and capturing appropriate objective evidence.Coaching assigned cross-functional team contacts on testing processes, tools, and best practices.
Report and investigate observations and defects, working with other members of the development team to establish root cause and options for correction.Provide and manage traceability evidence between requirements, tests and risk documentation.Write formal test plans and reports that can be used in submission packages to regulatory agencies.Generate and approve design history file documents, device master record documents, engineering change order records, and other quality system documents and records as assigned.Develop, disclose, and support the patenting of innovative technology and solutions.WHAT YOU CAN BRING TO OUR GREAT TEAMRequired:Bachelor's Degree in Engineering, Software, Computer Science, or related discipline or equivalent experience2+ years of similar experience, including software testing, test automation, verification experience and/or software development experience.Strong written and verbal communication skills with the ability to communicate with both internal and external stakeholders and senior leadership.Proficient with MS Office Suite (e.g., Word, Excel, Outlook, etc.)Preferred:Advanced level degree in Engineering, Software, Computer Science, or related disciplineClass III medical device experiencePrevious experience developing and/or testing embedded software architectures.Additional development experience utilizing .NET, C#, and/or C++.
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