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Internship 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

Follow Medical device regulations (IEC 62304, IEC 82304, FDA...etc.) * Provide leadership in ... Regular employees are those who are not temporary, such as interns. Temporary employees are ...

Senior Software Engineer -CRDN

Minneapolis, MN · On-site

$127K - $168K/yr

Follow Medical device regulations (IEC 62304, IEC 82304, FDA...etc.) * Provide leadership in ... Regular employees are those who are not temporary, such as interns. Temporary employees are ...

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 ...

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 ...

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

This position is responsible for software development and the maintenance of software applications associated with medical product systems. PRIMARY ACTIVITIES • Apply software engineering knowledge ...

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Internship Medical Device Software Engineer information

What is an internship medical device software engineer?

An Internship Medical Device Software Engineer is a student or recent graduate who assists in designing, developing, and testing software used in medical devices under the supervision of experienced engineers. Their responsibilities may include coding, debugging, documentation, and ensuring that the software complies with healthcare regulations and standards. This internship provides hands-on experience in both software engineering and the unique requirements of the medical device industry, helping interns learn about safety, reliability, and regulatory compliance. Interns also collaborate with cross-functional teams, such as hardware engineers and quality assurance specialists, to contribute to the overall development process.

What does an internship medical device software engineer do?

As an internship medical device software engineer, you can expect to work on a variety of tasks such as writing and testing code for embedded systems, developing user interfaces, and assisting with software verification and validation processes. You may also help document code, participate in team meetings, and collaborate with senior engineers, quality assurance, and regulatory teams to ensure compliance with industry standards. This hands-on experience provides valuable exposure to the full product development lifecycle and offers opportunities to learn about the unique challenges of developing software for regulated medical devices.

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

To thrive as an Internship Medical Device Software Engineer, you need a foundational understanding of software development principles, programming languages like C/C++ or Python, and coursework in biomedical engineering or computer science. Familiarity with industry-specific tools such as version control systems (e.g., Git), embedded systems, and compliance standards like IEC 62304 is highly valued. Strong problem-solving abilities, attention to detail, and effective teamwork skills set top candidates apart. These competencies are essential to ensure the development of reliable, regulatory-compliant software that supports patient safety and innovation in medical technology.

Can internship medical device software engineers work in the medical field?

Yes, internship medical device software engineers can work in the medical field, typically assisting in the development and testing of software for medical devices. They often work under supervision, gaining experience with regulatory standards like FDA requirements and using tools such as embedded systems and programming languages like C or Python.

Do internship medical device software engineer interns get paid?

Internship medical device software engineer interns are often paid, with compensation varying by company, location, and program duration. Many internships in this field offer stipends or hourly wages to attract qualified candidates and support their work on software development, testing, and regulatory compliance. However, some internships may be unpaid, so it is important to review specific program details.

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 are popular job titles related to Internship Medical Device Software Engineer jobs in Minnesota?

For Internship Medical Device Software Engineer jobs in Minnesota, the most frequently searched job titles are:

What job categories do people searching Internship Medical Device Software Engineer jobs in Minnesota look for?

The top searched job categories for Internship Medical Device Software Engineer jobs in Minnesota are:

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

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

Principal Embedded Software Engineer

Tactile Medical

Minneapolis, MN • On-site

Full-time

Posted 4 days ago


Tactile Medical rating

8.6

Company rating: 8.6 out of 10

Based on 11 frontline employees who took The Breakroom Quiz


Job description

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.

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