Software Engineering Manager - Cardiac Ablation Solutions

We anticipate the application window for this opening will close on - 28 Sep 2026 Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life At 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. The Software Engineering Manager will be an integral member of the Affera Software Team, working on cutting-edge technology in the electrophysiology field. This role offers a rare chance to be at the forefront of developing groundbreaking technology that can disrupt the industry. This role will lead a team responsible for designing, developing, testing, and maintaining software for the Affera mapping system, providing technical leadership, people management, and cross-functional execution oversight to deliver safe, high-quality, and innovative software solutions that support product performance, regulatory compliance, and business objectives. The ideal candidate will have deep experience leading software engineering teams in a regulated environment, with strong expertise in software architecture, product development, and team development. They will take ownership of key software capabilities while working collaboratively with cross-functional engineering teams and are passionate about developing products that will have a positive impact on the lives of millions. About the Affera Mapping and Ablation System The Affera Mapping and Ablation System is an innovative medical technology designed to treat patients with cardiac arrhythmias. The system involves advanced mapping techniques to create detailed images of the heart's electrical activity, helping physicians identify abnormal areas causing arrhythmias. Once identified , the Affera Ablation System delivers targeted energy to disrupt these abnormal signals, restoring normal heart rhythm. Primary Responsibilities Lead software engineering teams responsible for architecture, design, development , sustaining activities for complex medical device software. Define technical direction, development priorities, and execution plans in alignment with product and business strategy. Support planning and execution of release milestones, risk management, defect resolution, and continuous improvement while partnering with cross-functional teams to deliver robust solutions for current and future product releases. Define, plan, organize, and coordinate software development deliverables across multiple sites in accordance with FDA and other regulatory requirements. Recruit, coach, mentor, retain , and develop high-performing software engineering talent while fostering a culture of accountability, collaboration, innovation, and engineering excellence. Lead forecasting, effort estimation, resource planning, technical planning, execution, and release activities. Drive continuous improvement by identifying and implementing industry-standard software engineering technologies, methods, and tools. Apply software development methodologies, including Agile practices, to improve execution, collaboration, and delivery across the organization. Champion best practices in software development, architecture, cybersecurity, testability, and documentation. Oversee definition and implementation of software engineering practices that improve quality, maintainability, scalability, and product performance. Contribute to product strategy through technical assessment, roadmap input, and tradeoff analysis. Required Qualifications Bachelor's degree and a minimum of 7 years of relevant experience with 5+ years of managerial experience OR an advanced degree with a minimum of 5 years of relevant experience with 5+ years of managerial experience. Demonstrated ability to balance technical leadership, people management, execution discipline, and long-term engineering strategy. Familiarity with Python and C++. Thorough understanding of software architecture, design, implementation, code review, integration, and requirements traceability practices. Preferred Qualifications Strong knowledge of medical product software development, IEC-62304, and FDA guidance in a technical discipline, preferably software related (Computer Science, Computer Engineering, Electrical Engineering), with relevant software engineering experience in regulated product development. Strong understanding of good documentation practices, software lifecycle processes, configuration management, and commonly used engineering management tools. Ability to work with Quality, Regulatory, Systems, Test, and other engineering partners to ensure software deliverables meet product, compliance, and business needs. Ability to work with Systems, Mechanical, Electrical, and Software engineers when discovering, documenting, and resolving integration issues. Experience leading teams that develop complex software systems involving real-time performance, hardware integration, data visualization, or distributed system components. Experience with embedded software, real-time systems, imaging, mapping, or medical device platforms. Experience writing technical reports Strong work ethic and entrepreneurial drive Ability to work effectively in a fast-paced, collaborative environment. Strong communication skills, both written and verbal #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. Physical Job Requirements The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. U.S. Work Authorization & Sponsorship At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment. ‌ Recruitment Fraud Alert We are aware of phishing scams targeting job seekers. Please keep the following in mind: Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses. Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Securit