Quality Program Manager Visa Sponsorship Jobs in Minnesota
Quality program manager roles in Minnesota are concentrated in the Twin Cities metro, where medical device giants like Medtronic and Boston Scientific, along with manufacturers such as 3M and Ecolab, regularly hire for quality and compliance leadership. International candidates with engineering or quality management backgrounds will find active sponsorship activity across these sectors.
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INTRODUCTION
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 Life
Software Engineering Quality Program Manager
Careers That Change Lives
Transforming Patient Management with Smart Technology!
Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology can do to help alleviate pain, restore health, and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be. Be a part of a company that thinks differently to solve problems, make progress, and deliver meaningful innovations.
Cardiac Rhythm Management (CRM) Software develops the next generation medical technologies that alleviate pain, restore health and extend life for millions of patients across the world. 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.
CRM Software is developed with state of the art, industry standard technologies and used by Clinicians and Patients worldwide. In this exciting role as a Senior Software Program Manager, you will have responsibility for leading instrument software development program that support products in Cardiac Rhythm Management (CRM). These products include implantable cardiac devices (pacemakers, implantable defibrillators, cardiac re-synchronization devices and cardiac rhythm monitors). The Software Engineering Program Manager is accountable for ensuring software execution and delivery across agile/scrum teams within the Patient Care Systems organization.
This includes responsibility to guide instrument software/firmware development team(s) in their day-to-day development activities, provide program and project planning, scheduling and tracking, and help drive functional excellence in program execution for the Software organization. The candidate must be self-driven, with a strong understanding of project management, the Software Development Lifecycle process and strong technical and leadership skills.
This position is in Mounds View, MN. within the Cardiac Rhythm Management (CRM) 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.
Responsibilities
In general, the following responsibilities apply for the Software Engineering Quality 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 Team 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 member’s 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 – External
Must Have - Minimum Requirements
TO BE CONSIDERED FOR THIS ROLE, PLEASE BE SURE THE MINIMUM REQUIREMENTS ARE EVIDENT ON YOUR RESUME
- Bachelor’s of Science and minimum of 5 years of work experience in engineering and/or quality OR advanced degree in science with 3 years of work experience in engineering and/or quality.
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
Physical Job Requirements
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. (ADA-United States of America)
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.
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.
Join us in our mission to alleviate pain, restore health, and extend life—where your unique background and perspective are valued.
Benefits & Compensation
Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
Salary ranges for U.S (excl. PR) locations (USD): $150,400.00 - $225,600.00
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).
The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).
The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).
Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.

INTRODUCTION
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 Life
Software Engineering Quality Program Manager
Careers That Change Lives
Transforming Patient Management with Smart Technology!
Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology can do to help alleviate pain, restore health, and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be. Be a part of a company that thinks differently to solve problems, make progress, and deliver meaningful innovations.
Cardiac Rhythm Management (CRM) Software develops the next generation medical technologies that alleviate pain, restore health and extend life for millions of patients across the world. 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.
CRM Software is developed with state of the art, industry standard technologies and used by Clinicians and Patients worldwide. In this exciting role as a Senior Software Program Manager, you will have responsibility for leading instrument software development program that support products in Cardiac Rhythm Management (CRM). These products include implantable cardiac devices (pacemakers, implantable defibrillators, cardiac re-synchronization devices and cardiac rhythm monitors). The Software Engineering Program Manager is accountable for ensuring software execution and delivery across agile/scrum teams within the Patient Care Systems organization.
This includes responsibility to guide instrument software/firmware development team(s) in their day-to-day development activities, provide program and project planning, scheduling and tracking, and help drive functional excellence in program execution for the Software organization. The candidate must be self-driven, with a strong understanding of project management, the Software Development Lifecycle process and strong technical and leadership skills.
This position is in Mounds View, MN. within the Cardiac Rhythm Management (CRM) 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.
Responsibilities
In general, the following responsibilities apply for the Software Engineering Quality 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 Team 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 member’s 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 – External
Must Have - Minimum Requirements
TO BE CONSIDERED FOR THIS ROLE, PLEASE BE SURE THE MINIMUM REQUIREMENTS ARE EVIDENT ON YOUR RESUME
- Bachelor’s of Science and minimum of 5 years of work experience in engineering and/or quality OR advanced degree in science with 3 years of work experience in engineering and/or quality.
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
Physical Job Requirements
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. (ADA-United States of America)
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.
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.
Join us in our mission to alleviate pain, restore health, and extend life—where your unique background and perspective are valued.
Benefits & Compensation
Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
Salary ranges for U.S (excl. PR) locations (USD): $150,400.00 - $225,600.00
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).
The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).
The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).
Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
Quality Program Manager Job Roles in Minnesota
See all 51+ Quality Program Manager Jobs in Minnesota
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Search Quality Program Manager Jobs in MinnesotaQuality Program Manager Jobs in Minnesota: Frequently Asked Questions
Which companies sponsor visas for quality program managers in Minnesota?
Medtronic, Boston Scientific, and 3M are among Minnesota's most active sponsors for quality program manager roles, given the state's strong medical device and manufacturing sectors. Ecolab, Cargill, and General Mills also hire quality leadership roles and have established immigration sponsorship programs. These employers regularly file H-1B petitions for quality, compliance, and regulatory affairs positions requiring specialized technical degrees.
Which visa types are most common for quality program manager roles in Minnesota?
The H-1B is the most common visa for quality program managers in Minnesota, as these roles typically require a bachelor's degree or higher in engineering, science, or a related technical field, meeting the specialty occupation standard. Candidates with advanced degrees may also pursue EB-2 or EB-3 employment-based green card sponsorship after establishing tenure. TN visas are available to qualified Canadian and Mexican nationals in eligible engineering classifications.
Which cities in Minnesota have the most quality program manager sponsorship jobs?
The Minneapolis-Saint Paul metro area accounts for the large majority of quality program manager sponsorship activity in Minnesota. Specifically, suburban hubs like Fridley, Arden Hills, Maple Grove, and Maplewood host major medical device and manufacturing facilities where these roles are concentrated. Rochester, home to IBM and healthcare operations, also sees periodic openings. Smaller manufacturing centers in Greater Minnesota occasionally post quality leadership roles as well.
How to find quality program manager visa sponsorship jobs in Minnesota?
Migrate Mate filters job listings specifically by visa sponsorship availability, making it easier to identify Minnesota employers actively hiring quality program managers who will sponsor international candidates. Rather than sorting through thousands of general postings, you can focus on companies with verified sponsorship history in quality, compliance, and regulatory roles across the Twin Cities metro and other Minnesota manufacturing hubs.
Are there any state-specific considerations for quality program managers seeking sponsorship in Minnesota?
Minnesota's medical device industry is one of the most concentrated in the United States, which means quality program manager roles here often require familiarity with FDA quality system regulations and ISO 13485 standards, not just general quality management credentials. Employers filing H-1B petitions must meet Department of Labor prevailing wage requirements for the specific role and location. The University of Minnesota and Minnesota State system also supply a pipeline of engineering graduates, so competition for sponsored roles can be strong.
What is the prevailing wage for sponsored quality program manager jobs in Minnesota?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.
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