> Markdown version of [/jobs/ext/156010-sr-software-quality-engineer](https://www.wearedevelopers.com/jobs/ext/156010-sr-software-quality-engineer). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Sr. Software Quality Engineer - **Company:** Medtronic Inc. - **Location:** Mounds View, MN, United States - **Experience:** Expert - **Salary:** $103,200.0 - $154,800.0 - **Contract:** Temporary contract - **Skills:** Software Quality, Cyber Security, Linux, Failure Mode Effects Analysis, Python (Programming Language), Qt (Software), Reliability Engineering, Software Engineering, Test Scripts, Docker - **Published:** May 30, 2026 - **Apply:** https://www.juju.com/job/00000000g3iulb ## About the Role + Bachelor's degree anda minimum of4years of relevant experience + ORMaster'sdegree witha minimum of2years of relevant experience + OR PhD with 0 years relevant experience Preferred Qualifications + At least 1 year of experience supporting product development. + Though this is not a coding role, the ability to perform simple coding tasks and effectively read, interpret, and understand existing software codetocollaborate and execute necessary work with software engineers is needed + Excellent written and oral communication skills. + 2+ years of medical device or other regulated industry (such as defense or aerospace) experience. + 2+ years of industry experience working with a software development team + Experience creating risk analysis documentation such as FMEAs and FTAs. + Experience using or working with products built on Python, Qt, Docker, and Linux. + Strong knowledge of cybersecurity and the software lifecycle within regulated environments, including design, development, and post-market support. + Experience with cardiac and electrophysiology medical specialties. + Advanced degree in a relevant field. + Certification in quality systems or regulatory affairs (e.g., Six Sigma, ASQ, or similar). \#LI-MDT For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required. ## Description + Support software quality and reliability efforts for Cardiac Ablation Solutions products, ensuring compliance with regulatory standards such as FDA CFR, MDR, IEC 62304, and ISO 13485. + Serve asmemberof the extended quality team for Affera software releases used for mapping and navigation in electrophysiology procedures. Collaborate with other quality team members to take accountability for completing assigned functional work within program deadlines. + Review and approve various Design History File documents related to software and security, including requirements, design, development, integration, test protocols, test reports, verification, validation, and tooling. Ensure all documentation meets reliability standards and follows QMS processes. + Develop and review documentation for traceability, testability, and compliance according to standard operating procedures. + Developexpertisein assigned products and projects, including hands-on time in the engineering lab and participation in product training as assigned. + Participate in software risk analysis and defect assessments as assigned. + Contribute to tracking software quality metrics for assigned programs, supporting continuous monitoring and improvement of quality outcomes to achieve required levels of product reliability. + Provide software quality support for post-market activities and analysis, including work supporting issue assessments, health risk assessments, and CAPAs. + Recommend design or test methods to achieveappropriate levelsof product reliability and security.Propose changes to design or testing as necessary to improve software and/or process reliability. + Contribute to reliability engineering program strategies to achieve Medtronic, customer, and regulatory reliabilityobjectivesfor assigned programs. + Review and support strategies for product security testing as assigned. + As available, attend a live EP case at least once per year to enhance workflow and product knowledge. Regularlyparticipatein virtuallivecase learning opportunities. + Collaborate with cross-functional teams, including R&D, regulatory affairs, and clinical teams, to ensure alignment on quality and compliance requirements. ## Related Videos - [Docker network without Docker](https://www.wearedevelopers.com/videos/1418-docker-network-without-docker) - [More efficient software for more efficient microchips](https://www.wearedevelopers.com/videos/1164-more-efficient-software-for-more-efficient-microchips) - [Are Classical Automation Frameworks Dead? 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