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Internship Medical Device Software Engineer Jobs

Spruce Infotech

Software Engineer C++

Arden Hills, MN · On-site

... 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 ...

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Internship Medical Device Software Engineer information

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$13

$25

$38

How much do internship medical device software engineer jobs pay per hour?

As of Jul 16, 2026, the average hourly pay for internship medical device software engineer in the United States is $25.42, according to ZipRecruiter salary data. Most workers in this role earn between $20.67 and $28.85 per hour, depending on experience, location, and employer.

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 types of projects and responsibilities can I expect as an Internship Medical Device Software Engineer?

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, and why are they important?

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.
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Internship Medical Device Software Engineer jobs near you
Infographic showing various Internship Medical Device Software Engineer job openings in the United States as of July 2026, with employment types broken down into 13% Internship, 47% Full Time, and 40% Contract. Highlights an 100% In-person job distribution, with an average salary of $52,867 per year, or $25.4 per hour.
Principal Embedded Software Engineer

Principal Embedded Software Engineer

CUTERA INC

Brisbane, CA

Full-time

Re-posted 17 days ago

Job description

Position Summary:

We are seeking a highly experienced Principal Embedded Software Engineer to lead the design and development of embedded software for medical device systems. This role focuses on delivering safe, reliable, and high-performance software in compliance with regulatory standards, including ISO 62304.

As a key member of our R&D organization, you will translate system requirements into robust embedded software solutions, partnering closely with cross-functional engineering and quality teams. Your work will directly support new product development, design transfer, and lifecycle maintenance of regulated medical devices, ensuring quality, safety, and performance.

Duties & Responsibilities:

  • Lead embedded software development activities across the full medical device lifecycle in accordance with ISO 62304.
  • Collaborate with hardware, systems, and quality engineering teams to define system architecture, software requirements, and design specifications.
  • Design, develop, and maintain embedded software primarily in C and C++ for microcontroller and processor-based systems.
  • Participate in requirements definition, risk analysis, and traceability to ensure compliance with regulatory standards.
  • Develop and execute software verification and validation activities, including unit testing, integration testing, and system-level testing.
  • Support design reviews and ensure adherence to design control processes.
  • Contribute to software documentation, including requirements, architecture, design, and test artifacts.
  • Support new product introduction (NPI), design transfer, and sustaining engineering activities.
  • Troubleshoot and resolve software defects across development and production environments.
  • Ensure compliance with applicable regulatory and quality standards through structured development and documentation practices.
  • Other duties as needed or required.

Minimum Requirements & Qualifications: 

  • Bachelor’s or Master’s degree in Electrical Engineering, Computer Science, or a related field, with 12+ years of experience in embedded software development.
  • Strong experience in medical device software development compliant with ISO 62304.
  • Deep expertise in embedded systems, microprocessor-based controller design and fault finding and resolution.
  • Advanced proficiency in C and C++ for embedded applications.
  • Experience with real-time operating systems (RTOS) and/or bare-metal development.
  • Strong ability to read and interpret electronic schematics and component datasheets.
  • Experience with software verification and validation methodologies in regulated environments.
  • Familiarity with risk management processes (e.g., ISO 14971) and design control practices.
  • Experience working in cross-functional teams including hardware, systems, quality, and manufacturing engineering.
  • Proficiency with debugging tools, version control systems, and embedded development toolchains.
  • Experience supporting product lifecycle activities, including sustaining engineering and post-market support.

Preferred Qualifications:

  • Serial communications RS422, SPI, I2C.
  • Closed loop controller (PID) design.
  • Wireless communication (Wi-Fi and cellular).
  • Data encryption.
  • OTA software updates.
  • Embedded graphics development with Qt, LVGL or other framework.

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