About the role
We anticipate the application window for this opening will close on - 17 Aug 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
Senior Software Engineering Program Manager
Careers That Change Lives
At Medtronic, we value what makes you unique. Be part of a company that thinks differently to solve problems, make progress, and deliver meaningful innovations.
As part of Interventional Cardiology Therapies (ICT), we are united by a shared purpose to bring life-changing therapies across Renal Denervation (RDN), Coronary and Structural Heart to more patients around the world. Guided by the Medtronic Mission—to alleviate pain, restore health, and extend life—we are building a more connected ICT organization that leverages the strength of our people, capabilities, and portfolio to drive meaningful impact for patients, physicians, and healthcare systems.
In this highly visible role as a Quality Core Team Member - Software Quality, you will serve as the primary Quality representative on cross-functional software product development teams, partnering with engineering, regulatory, clinical, and operations stakeholders to ensure quality is embedded throughout the software development lifecycle.
You will provide quality leadership for software design controls, risk management, verification and validation activities, cybersecurity, defect management, and product release decisions while ensuring compliance with global quality system and regulatory requirements.
As a trusted member of the Core Team, you will help drive alignment, proactively manage risk, and enable effective decision-making across complex development programs.
You will also partner with Quality Systems, Regulatory, and functional stakeholders to further evolve the Quality Management System (QMS), enabling software innovation while ensuring continued compliance with global regulatory standards and industry best practices.
This role requires deep technical expertise, leadership, and collaboration skills to balance innovation, quality, compliance, and speed to market. Through a commitment to quality excellence and continuous improvement, you will play a critical role in delivering software-enabled products and supporting strategic programs across the ICT portfolio.
This position is in Mounds View, MN. within the Coronary & Renal Denervation (CRDN) operating unit. 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 are working on-site 4 days per week 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 role will require less than 10% of travel to enhance collaboration and ensure successful completion of projects.
We believe that when people from different cultures, genders, and points of view come together, innovation is the result —and everyone wins. Medtronic walks the walk, creating an inclusive culture where you can thrive.
A Day in the Life
In general, the following responsibilities apply for the Senior Software Engineering Program Manager role. This includes, but is not limited to the following:
- Responsible for program estimation and planning including identifying requirements, developing work plans, managing program annual and strategic budgets, building schedules, and partnering with team members to determine and communicate functional and/or resource requirements.
- Own and Manage execution against an aggressive but achievable program and/or project plan, provide work direction to team members, work with peer program managers, cross functional program team members to monitor dependencies and ensure critical program milestones and deliverables are met.
- Collaborate with Core Team Leaders, Platform Leaders, Product Owners, Human Factors Engineer, Architects & Systems Engineers to drive program within scope, cost, and schedule
- Lead team(s) of software engineers (employees and vendor resources) to deliver on program commitments
- Communicate program status and issues to internal and external stakeholders regularly including the Core Tam Leader and Development Lead in the Program Core Team as appropriate. Proactively manage quality, risks, and issues at all stages in the program
- Provide input for setting team members’ performance objectives and provide feedback to the functional leaders about performance against project deliverables and core competencies.
- Conduct Scrum events including sprint planning, daily stand-ups, sprint review and retrospective.
Qualifications –
Must Have - Minimum Requirements
TO BE CONSIDERED FOR THIS ROLE, PLEASE BE SURE THE MINIMUM REQUIREMENTS ARE EVIDENT ON YOUR RESUME
- Bachelor’s degree in science, technology, engineering, or math and minimum of 7 years of technical work experience OR advanced degree in science, technology, engineering, or math, with 5 years of technical experience.
Nice to Have
- 5+ years of experience leading software development projects within Med-Tech industry
- Strong understanding of software and embedded systems
- Demonstrated track record of successfully delivering on projects in a matrix environment
- Understanding of the Software Development Life Cycle
- Experience managing geographically distributed teams
- Track record of effective vendor management to deliver results
- Experience as a Scrum Master in SW teams and Scrum Master Certification
- Project Management Certification such as PMP
- Experience working in regulated environments and delivering new products in compliance with global regulatory standards
About Medtronic
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.
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