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Medical Device Software Engineer Jobs in Minnesota

... medical device systems. Work with a team of highly skilled engineers to deliver groundbreaking ... Develop software for testing platforms and complex software tools. * Integrate software designs ...

Senior Software Engineer -CRDN

Minneapolis, MN · On-site

$127K - $168K/yr

A Day in the Life Senior Software Engineer Careers that Change Lives Transforming Patient ... Follow Medical device regulations (IEC 62304, IEC 82304, FDA...etc.) * Provide leadership in ...

Senior Software Engineer -CRDN

Minneapolis, MN · On-site

$127K - $168K/yr

A Day in the Life Senior Software Engineer Careers that Change Lives Transforming Patient ... Follow Medical device regulations (IEC 62304, IEC 82304, FDA...etc.) * Provide leadership in ...

Senior Software Engineer -CRDN

Minneapolis, MN · On-site

$127K - $168K/yr

A Day in the Life Senior Software Engineer Careers that Change Lives Transforming Patient ... Follow Medical device regulations (IEC 62304, IEC 82304, FDA...etc.) * Provide leadership in ...

Provide technical support for all phases of the medical device software lifecycle, including ... C programming for embedded systems, including ARM based microcontrollers. * Systems engineering ...

Provide technical support for all phases of the medical device software lifecycle, including ... C programming for embedded systems, including ARM based microcontrollers. * Systems engineering ...

Sr. Embedded Software Engineer

Saint Paul, MN · On-site

$125K - $164K/yr

Provide technical support for all phases of the medical device software lifecycle, including ... C programming for embedded systems, including ARM based microcontrollers. * Systems engineering ...

Sr. Embedded Software Engineer

New Brighton, MN · On-site

$131K - $171K/yr

Provide technical support for all phases of the medical device software lifecycle, including ... C programming for embedded systems, including ARM based microcontrollers. * Systems engineering ...

Sr. Embedded Software Engineer

New Brighton, MN · On-site

$131K - $171K/yr

Provide technical support for all phases of the medical device software lifecycle, including ... C programming for embedded systems, including ARM based microcontrollers. * Systems engineering ...

Sr. Principal Software Engineer

Fridley, MN · On-site

$129K - $178K/yr

Working in a highly regulated medical device environment, you will contribute to the full software ... Establish engineering standards, best practices, and development frameworks across teams * Designs ...

Sr. Principal Software Engineer

Fridley, MN · On-site

$129K - $178K/yr

Working in a highly regulated medical device environment, you will contribute to the full software ... Establish engineering standards, best practices, and development frameworks across teams * Designs ...

Principal Software Engineer

Fridley, MN · On-site

$139K - $186K/yr

Medtronic Pelvic Health As a Principal Software Engineer, you will design, develop, and verify web ... Working in a highly regulated medical device environment, you will contribute to the full software ...

Principal Software Engineer

Fridley, MN · On-site

$139K - $186K/yr

Medtronic Pelvic Health As a Principal Software Engineer, you will design, develop, and verify web ... Working in a highly regulated medical device environment, you will contribute to the full software ...

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Showing results 1-20

Medical Device Software Engineer information

See Minnesota salary details

$62.2K

$144.5K

$201.3K

How much do medical device software engineer jobs pay per year?

As of Aug 27, 2026, the average yearly pay for medical device software engineer in Minnesota is $144,486.00, according to ZipRecruiter salary data. Most workers in this role earn between $117,500.00 and $169,400.00 per year, depending on experience, location, and employer.

What is a medical device software engineer?

A Medical Device Software Engineer is responsible for designing, developing, testing, and maintaining software used in medical devices. They ensure compliance with regulatory standards like FDA and IEC 62304 while working on embedded systems, user interfaces, or cloud-based healthcare applications. Their role involves collaborating with cross-functional teams, including hardware engineers and regulatory specialists, to ensure patient safety and product effectiveness.

What are the typical daily responsibilities of a medical device software engineer?

Medical Device Software Engineers typically spend their days designing, coding, and testing software for medical devices in compliance with health regulations. They collaborate closely with hardware engineers, quality assurance teams, and regulatory specialists to ensure that the software integrates seamlessly with device hardware and meets performance and safety standards. Documenting development processes, participating in code reviews, and addressing feedback from cross-functional teams are also common aspects of the role. This position often requires troubleshooting issues in both simulated and real clinical environments to ensure the reliability and safety of the device.

What are the key skills and qualifications needed to thrive as a medical device software engineer?

To thrive as a Medical Device Software Engineer, you need a solid background in software development, embedded systems, and biomedical engineering, often supported by a degree in computer science, electrical engineering, or a related field. Experience with programming languages like C/C++, knowledge of real-time operating systems, and familiarity with medical device regulatory standards such as IEC 62304 are typically required. Strong problem-solving skills, attention to detail, and effective communication are essential soft skills for this position. These skills ensure high-quality, compliant software that contributes to safe and reliable medical devices, which are critical for patient health.

What are the most commonly searched types of Medical Device Software Engineer jobs in Minnesota?

The most popular types of Medical Device Software Engineer jobs in Minnesota are:

What cities in Minnesota are hiring for Medical Device Software Engineer jobs?

Cities in Minnesota with the most Medical Device Software Engineer job openings:

Infographic showing various Medical Device Software Engineer job openings in Minnesota as of August 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $144,486 per year, or $69.5 per hour.

Principal Embedded Software Engineer

Tactile Medical

Minneapolis, MN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 2 days ago

New


Tactile Medical rating

8.6

Company rating: 8.6 out of 10

Based on 11 frontline employees who took The Breakroom Quiz


Job description

At Tactile Medical, we specialize in developing at-home therapy devices to treat lymphedema, chronic venous insufficiency and respiratory illnesses.
Position Summary
At Tactile Medical, we specialize in developing at-home therapy devices to treat lymphedema, chronic venous insufficiency, and respiratory illnesses. The Principal Embedded Software Engineer provides technical leadership for the firmware and embedded software used in regulated medical devices. This role is responsible for guiding embedded software architecture, supporting development across bare-metal and RTOS-based platforms, and helping establish future embedded Linux and connected device capabilities while ensuring software is developed with the rigor required for regulated medical device development.
Responsibilities
  • Lead the design, development, debugging, integration, and maintenance of embedded software for Class II regulated medical device products.
  • Define and evolve embedded software architecture, module boundaries, interfaces, design patterns, and technical standards that support reliability, maintainability, testability, cybersecurity, and long-term product support.
  • Provide technical leadership for connected device capabilities, including Wi-Fi and Bluetooth connectivity, mobile/cloud integration, provisioning, diagnostics, telemetry, secure updates, and data exchange across firmware, mobile, and cloud systems.
  • Develop embedded software in C/C++ for microcontroller, RTOS, bare-metal, and resource-constrained environments while helping evaluate and establish future embedded Linux platform capabilities.
  • Create clear software architecture, design specification, interface definition, traceability, verification, cybersecurity, and release documentation that supports regulated product development and submission readiness.
  • Contribute to platform-level decisions involving bootloaders, device drivers, board support packages, middleware, communication stacks, diagnostics, software update mechanisms, and device application behavior.
  • Provide technical guidance and mentorship through design reviews, code reviews, implementation planning, troubleshooting, and technical trade-off decisions.
  • Improve embedded software engineering practices related to source control, peer review, static analysis, unit testing, automated builds, CI/CD, release readiness, defect prevention, and post-release support.
Required Qualifications
  • Bachelor's degree in Computer Engineering, Computer Science, or a related technical discipline.
  • 10+ years developing embedded firmware, embedded software, or device software for commercial products.
  • Senior technical leadership background, including leading embedded software design decisions, mentoring engineers, setting technical direction, or serving as a technical lead for complex product development efforts.
  • Strong proficiency in C/C++ development for microcontrollers, RTOS, bare-metal systems, or resource-constrained embedded environments.
  • Depth in embedded software architecture, module design, interface definition, state machines, communication protocols, diagnostics, embedded debugging, and hardware/software integration.
  • Regulated product development background, with knowledge of medical device software lifecycle expectations such as IEC 62304, design controls, requirements traceability, software verification, risk management, and design history file documentation.
  • Clear written and verbal communication skills, with the ability to explain complex technical issues, risks, and trade-offs to technical and non-technical stakeholders.
Preferred Qualifications
  • Class II medical device software development, preferably for products cleared through the FDA 510(k) pathway.
  • Embedded Linux background, including board support packages, kernel configuration, device drivers, bootloaders, root file systems, Yocto, Buildroot, or similar platform technologies.
  • FDA 510(k) software documentation contributions, including software architecture, software design specifications, requirements, traceability, verification evidence, cybersecurity documentation, and release documentation.
  • Secure embedded software development practices such as secure boot, signed updates, vulnerability management, SBOM/SOUP concepts, and medical device cybersecurity guidance.
  • Connected device architecture, device provisioning, diagnostics, telemetry, over-the-air updates, mobile/cloud integration, or edge-to-cloud workflows.

Our total compensation package includes medical, dental and vision benefits, retirement benefits, employee stock purchase plan, paid time off, parental leave, family medical leave, volunteer time off and additional leave programs, life insurance, disability coverage, and other life and work wellness benefits and discounts. Benefits may be subject to generally applicable eligibility, waiting period, contributions, and other requirements and conditions.
Below is the starting salary or hourly range for this position, although offers may differ based on the candidate's location, job-specific knowledge, skills and experience.
US Pay Range
$115,600-$173,250 USD
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