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Medical Device Software Engineer Jobs (NOW HIRING)

... 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 ...

... regulated medical device software. These systems will support the full software lifecycle, from ... Partner closely with software engineering teams to embed: * Compliance with CI/CD pipelines

Lead and manage a team of software engineers delivering medical device software solutions. * Own Agile delivery execution, including sprint planning, tracking and on-time delivery. * Drive end-to-end ...

Software Engineer III

Monroeville, PA

$57 - $76.50/hr

Software applications are developed for the Web, Client Server, Android and IOS platforms. OUTCOMES ... Analyzing and verifying medical device designs. * *Writing detailed automated and manual test ...

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Medical Device Software Engineer information

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$63.5K

$147.5K

$205.5K

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

As of Jul 7, 2026, the average yearly pay for medical device software engineer in the United States is $147,524.00, according to ZipRecruiter salary data. Most workers in this role earn between $120,000.00 and $173,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Medical Device Software Engineer position, and why are they important?

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 is a Medical Device Software Engineer job?

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 some 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 cities are hiring for Medical Device Software Engineer jobs? Cities with the most Medical Device Software Engineer job openings:
What are the most commonly searched types of Medical Device Software Engineer jobs? The most popular types of Medical Device Software Engineer jobs are:
What states have the most Medical Device Software Engineer jobs? States with the most job openings for Medical Device Software Engineer jobs include:
Principal Embedded Software Engineer

Principal Embedded Software Engineer

Cutera, Inc.

Brisbane, CA • On-site

Full-time

Posted 8 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.