Software Quality Engineer II

We anticipate the application window for this opening will close on - 28 Oct 2025 At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.A Day in the LifeAt Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We're working a minimum of 4 days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary.*This will sit out of our Independence, OH office* Join Medtronic as a Software Quality Engineer II and be at the forefront of transforming lives through advanced medical technology In this dynamic role, you'll work alongside a team of engineers and cross-functional partners to drive quality for design, development, and maintenance of operating systems and manufacturing/service tooling software releases for Affera cardiac electrophysiology systems . By blending technical expertise with a passion for quality, compliance, and improving patient outcomes, you'll have the opportunity to impact global healthcare as the usage of Affera grows rapidly worldwide.Primary ResponsibilitiesSupport 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 as a member of the extended quality team for operating system and service/ manufacturing tooling software releases across the Affera portfolio . 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.Develop expertise in assigned products and projects, including hands-on time in the engineering lab and participation in product training as assigned.Participate in software and process 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 achieve appropriate levels of 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 reliability objectives for assigned programs.Review and support strategies for product security testing as assigned.As business needs permit, periodically visit manufacturing and servicing facilities to aid in understanding of quality processes related to software loading and tooling .Regularly participate in virtual electrophysiology patient case learning opportunities.Collaborate with cross-functional teams, including R&D, regulatory affairs, and clinical teams, to ensure alignment on quality and compliance requirements.Travel Requirements