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Junior Medical Device Software Engineer Jobs (NOW HIRING)

Leo Cancer Care Ltd

WI · On-site

$122K - $162K/yr

This role sits at the intersection of medical device software engineering and clinical systems integration, with a primary focus on DICOM-RT interoperability between our treatment system and the ...

IT America Inc

Staff Software Engineer

Hercules, CA · On-site

Mentor junior and mid-level software engineers by sharing best practices in embedded development ... Background in laboratory equipment, clinical diagnostics, or medical device development.

Nova Biomedical

Software Engineer Manager

Norwood, MA · On-site

The Software Engineer Manager will also help bring biotechnology software development capabilities ... Manage software development activities throughout the complete medical device product lifecycle ...

Diality

Director, Software Engineering

Irvine, CA · Hybrid

$223K - $260K/yr

... software engineer contractors. * Familiarity with cloud-connected medical device systems, mobile applications, interoperability, healthcare data platforms, and device-to-cloud communication ...

Diality Inc

Director, Software Engineering

Irvine, CA · On-site

$223K - $260K/yr

... software engineer contractors. * Familiarity with cloud-connected medical device systems, mobile applications, interoperability, healthcare data platforms, and device-to-cloud communication ...

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Junior Medical Device Software Engineer information

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$46.5K

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

As of Sep 15, 2026, the average yearly pay for junior medical device software engineer in the United States is $94,542.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,000.00 and $95,500.00 per year, depending on experience, location, and employer.

What does a junior medical device software engineer do?

A Junior Medical Device Software Engineer assists in designing, developing, testing, and maintaining software for medical devices under the supervision of senior engineers. They help ensure that the software meets regulatory standards for safety and performance. Their work may involve writing code, debugging, documenting processes, and collaborating with cross-functional teams such as hardware engineers and quality assurance. This role is ideal for recent graduates or those with a few years of experience looking to build a career in the intersection of healthcare and technology.

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

To thrive as a Junior Medical Device Software Engineer, you need a solid background in software development (often with a degree in computer science or biomedical engineering), knowledge of medical device regulations, and familiarity with embedded systems. Experience with programming languages like C/C++, development environments, and compliance with standards such as IEC 62304 are typically required. Attention to detail, problem-solving abilities, and strong teamwork and communication skills help you excel in this role. These competencies are essential to ensure the safe, effective, and compliant development of medical device software in a highly regulated industry.

What are some common challenges faced by junior medical device software engineers in their first year on the job?

Junior Medical Device Software Engineers often encounter challenges such as adapting to strict regulatory standards, learning thorough documentation practices, and understanding the complexities of safety-critical software development. Working in multidisciplinary teams, they must quickly become proficient in both software engineering and medical device compliance, such as FDA or ISO standards. Successfully navigating these challenges requires strong communication skills, attention to detail, and a willingness to learn from senior engineers and cross-functional colleagues.

What is the difference between Junior Medical Device Software Engineer vs Medical Device Software Engineer?

AspectJunior Medical Device Software EngineerMedical Device Software Engineer
Required CredentialsTypically an entry-level degree (BSc or MSc) in Software Engineering, Biomedical Engineering, or related fields; may include basic certificationsSame as junior, but often with more professional experience or advanced certifications
Work EnvironmentSupportive team settings within medical device companies or healthcare tech firmsMore independent roles with increased responsibility in design, testing, and validation
Employer & Industry UsageCommonly used in medical device manufacturing, healthcare technology companies, and startupsUsed across medical device companies, regulatory bodies, and R&D departments

The main difference between a Junior Medical Device Software Engineer and a Medical Device Software Engineer lies in experience and responsibility. Junior roles focus on learning and supporting development tasks, while the more experienced engineer takes on complex design and validation responsibilities.

What cities are hiring for Junior Medical Device Software Engineer jobs?

Cities with the most Junior 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 Junior Medical Device Software Engineer jobs?

States with the most job openings for Junior Medical Device Software Engineer jobs include:

What are popular job titles related to Junior Medical Device Software Engineer jobs?

For Junior Medical Device Software Engineer jobs, the most frequently searched job titles are:

Infographic showing various Junior Medical Device Software Engineer job openings in the United States as of July 2026, with employment types broken down into 77% Full Time, 14% Part Time, and 9% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $94,542 per year, or $45.5 per hour.

Principal Embedded Software Engineer

Minneapolis, MN • On-site

Tactile Medical
Medical Equipment and Supplies Manufacturing • 1 - 5K employees
Learn more about Tactile Medicalexternal

Full-time

Posted 21 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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