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Medical Device Embedded Software Engineer Jobs (NOW HIRING)

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

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 ...

Embedded software engineer

Brisbane, CA · On-site

$158K - $208K/yr

The Sr. Embedded Software Engineer serves on the R&D team to contribute toward the development of ... Participate in medical device design activities, including development of new device requirements ...

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

Embedded software engineer

Brisbane, CA · On-site

$158K - $208K/yr

The Sr. Embedded Software Engineer serves on the R&D team to contribute toward the development of ... Participate in medical device design activities, including development of new device requirements ...

Embedded Software Engineer

Irvine, CA · On-site

$141K - $185K/yr

Embedded Software Engineer Location: Irvine, California (onsite) Duration: Long Term Contract ... Work closely with hardware teams on board bring-up, OS bring-up, and device driver development

Embedded Software Engineer Join our dynamic team as an Embedded Software Engineer where you will be ... Collaborate in a safety-critical environment, such as medical device or aerospace industries.

Embedded Software Engineer Join our dynamic team as an Embedded Software Engineer where you will be ... Collaborate in a safety-critical environment, such as medical device or aerospace industries.

Showing results 21-40

Medical Device Embedded Software Engineer information

See salary details

$70K

$153.4K

$174K

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

As of Aug 23, 2026, the average yearly pay for medical device embedded software engineer in the United States is $153,383.00, according to ZipRecruiter salary data. Most workers in this role earn between $131,500.00 and $173,000.00 per year, depending on experience, location, and employer.

What is a medical device embedded software engineer?

Medical Device Embedded Software Engineers are professionals who design, develop, and maintain the specialized software that runs on hardware inside medical devices, such as pacemakers, infusion pumps, and imaging machines. They ensure that the software meets strict regulatory standards for safety, reliability, and performance. Their work involves programming, testing, debugging, and documenting embedded code, as well as collaborating with hardware engineers and regulatory teams to bring safe and effective medical products to market.

What are the key skills and qualifications needed to thrive as a medical device embedded software engineer, and why are they important?

To thrive as a Medical Device Embedded Software Engineer, you need a strong background in embedded systems design, C/C++ programming, and a degree in electrical engineering, computer engineering, or a related field. Familiarity with real-time operating systems (RTOS), hardware-software integration, and industry standards like IEC 62304 or FDA regulations is typically required. Attention to detail, strong problem-solving abilities, and effective teamwork are vital soft skills for this role. These competencies are crucial for developing reliable, safe, and compliant software that meets stringent healthcare requirements.

What are some common challenges faced by medical device embedded software engineers when working on cross-functional teams?

Medical Device Embedded Software Engineers often collaborate closely with hardware engineers, regulatory specialists, and quality assurance teams. A common challenge is ensuring that software requirements align with hardware limitations and regulatory standards, which can necessitate frequent adjustments and clear documentation. Additionally, balancing the pace of software development with the rigorous testing and validation processes required for medical devices can be demanding. Effective communication and adaptability are essential to navigate these multidisciplinary interactions and deliver safe, compliant products.

What is the difference between Medical Device Embedded Software Engineer vs Firmware Engineer?

AspectMedical Device Embedded Software EngineerFirmware Engineer
CredentialsBachelor's in Electrical, Computer Engineering, or related; often certifications in medical device standardsBachelor's in Electrical, Computer Engineering, or related; certifications vary by industry
Work EnvironmentMedical device companies, regulated environments, quality assurance focusConsumer electronics, industrial, or embedded systems companies
Industry UsagePrimarily in healthcare, medical device manufacturingBroader tech sectors, including consumer electronics and industrial systems
Search & Comparison IntentHigh overlap in embedded systems, safety standards, and certification requirements

The Medical Device Embedded Software Engineer and Firmware Engineer roles share core skills in embedded systems development. However, the Medical Device Embedded Software Engineer focuses specifically on medical device safety, regulatory compliance, and working within healthcare environments. Firmware Engineers may work across various industries without the strict medical standards, making the Medical Device Embedded Software Engineer role more specialized in healthcare applications.

More about Medical Device Embedded Software Engineer jobs

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

Cities with the most Medical Device Embedded Software Engineer job openings:

What states have the most Medical Device Embedded Software Engineer jobs?

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

Infographic showing various Medical Device Embedded Software Engineer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, and 7% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $153,383 per year, or $73.7 per hour.

$130K - $171K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 11 days ago


Job description

At Zepto Life Technology, Inc. (Zepto), we are dedicated to revolutionizing healthcare through the development of innovative point-of-care molecular diagnostics. Our cutting-edge platform leverages giant magnetoresistance (GMR) technology as a sensitive and scalable detection method to improve the accuracy, speed, and accessibility of disease diagnosis. By integrating breakthroughs in biotech, assay development, engineering, and software, Zepto is shaping the future of molecular diagnostics in diverse settings and empowering more accessible, efficient healthcare innovation.


Summary

Zepto Life Technology is seeking an experienced and highly motivated Embedded Software Engineer to lead the design, development, and lifecycle management of embedded firmware for our next-generation molecular diagnostic instrumentation.

This individual will serve as the technical owner of the instrument's embedded software platform, developing firmware that controls hardware operation, acquires and processes data, manages instrument workflows, and enables communication between the electronics and higher-level software applications. The ideal candidate has extensive experience developing embedded systems for complex instruments and enjoys collaborating closely with electrical, software, assay, and systems engineers to bring innovative medical devices from concept through commercialization.


Essential Duties

Work under general direction while collaborating with multidisciplinary engineering teams to develop and commercialize Zepto's molecular diagnostic instrumentation, including but not limited to:

  • Serve as the technical owner of the embedded software and firmware architecture for Zepto's GMR diagnostic platform.
  • Design, develop, test, and maintain embedded firmware supporting instrument operation and control.
  • Develop low-level device drivers and hardware abstraction layers (HAL) for sensors, processors, peripherals, and communication interfaces.
  • Design firmware architecture that is scalable, maintainable, and compliant with medical device software development practices.
  • Define and implement instrument workflows, operational sequences, state machines, and timing logic.
  • Develop firmware supporting system startup, initialization, calibration, diagnostics, assay execution, error handling, and shutdown.
  • Design and optimize data acquisition, data buffering, data validation, and communication between embedded firmware and application software.
  • Collaborate with software engineering teams to define APIs, communication protocols, command structures, and software interfaces.
  • Collaborate closely with the Senior Electrical Systems Engineer during hardware bring-up, board validation, and system integration.
  • Implement firmware supporting GMR sensor data acquisition and signal processing algorithms.
  • Troubleshoot embedded software, firmware, and hardware integration issues using oscilloscopes, logic analyzers, debuggers, and other engineering tools.
  • Perform root cause analysis and implement corrective actions for software and system-level issues.
  • Develop and execute unit testing, integration testing, system testing, and software verification activities.
  • Develop and maintain software design documentation, architecture documents, software requirements, verification protocols, and technical records.
  • Support software risk management activities including Software FMEA, hazard analysis, and cybersecurity risk assessments where applicable.
  • Support FDA submissions by preparing software documentation required for Design Controls, Design History Files (DHF), and software lifecycle documentation.
  • Collaborate with Quality Assurance and Regulatory Affairs to ensure compliance with FDA Quality Management System Regulation and other applicable standards.
  • Participate in design reviews and provide technical leadership for embedded software architecture and best practices.
  • Perform other duties and special projects as assigned.


Required Education and Experience

  • Bachelor's degree in Computer Engineering, Electrical Engineering, Computer Science, Software Engineering, or a closely related discipline.
  • Minimum five (5) years of professional experience designing electronic hardware.
  • Strong proficiency in C and C++ programming for embedded systems.
  • Experience working with hardware vendor-provided IDEs and their programming or assembly language for embedded system prototyping and troubleshooting.
  • Experience developing firmware for microcontrollers, processors, or embedded Linux platforms.
  • Experience developing low-level hardware drivers and hardware abstraction layers (HAL).
  • Experience with embedded debugging tools, oscilloscopes, logic analyzers, and JTAG/SWD debuggers.
  • Experience implementing multithreaded or real-time embedded systems.
  • Strong troubleshooting and root cause analysis skills.
  • Experience using Git or other source code management systems.
  • Strong technical writing and documentation skills.
  • Demonstrated ability to independently manage complex engineering projects.


Preferred Education and Experience

  • Master's degree in Computer Engineering, Electrical Engineering, Computer Science, or related discipline.
  • Medical device development experience.
  • Experience supporting FDA-regulated product development.
  • Experience with molecular diagnostic or life science instrumentation.
  • Experience developing sensor-based electronic systems.
  • Familiarity with Giant Magnetoresistance (GMR) sensor technology.
  • Experience with Python or scripting languages for automation and testing.


Competencies

  • Strong technical leadership and ownership mindset.
  • Excellent analytical and problem-solving skills.
  • Ability to lead complex engineering projects from concept through commercialization.
  • Exceptional troubleshooting and root cause analysis skills.
  • Ability to communicate effectively across engineering, quality, regulatory, manufacturing, and executive teams.
  • Strong technical writing and documentation skills.


Work Environment

  • This position is based in a research and development laboratory and engineering environment where strict adherence to corporate policies, quality systems, and safety procedures is required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
  • The work environment includes laboratory instrumentation, electronic test equipment, prototype assembly areas, and manufacturing support activities.
  • The noise level in the work environment is typical for laboratory and engineering environments.
  • There is minimal exposure to Blood-borne Pathogens.
  • Exposure to Infectious Diseases is mitigated through the proper use of Personal Protective Equipment (PPE).
  • Occasional exposure to soldering equipment, electronic components, laboratory chemicals, cleaning agents, and manufacturing equipment may occur.


Job Type

  • Pay Range:
    $85,000-$110,000
    annually. Compensation is based on several factors including education, experience, technical expertise, leadership capabilities, and overall qualifications.
  • FLSA Status: Exempt, Monday-Friday 9:00am - 5:30pm (half-hour unpaid lunch), onsite.
  • Full-time employees are eligible for benefits including holiday time off, paid time off (PTO), sick time off, health insurance (medical, dental, and vision), health savings account (HSA), 401(k), and life insurance.
  • Some traveling may be required.


E-Verify

Zepto Life Technology participates in the U.S. Department of Homeland Security E-Verify program in all facilities located in the United States and certain U.S. territories. The E-Verify program is an Internet-based employment eligibility verification system operated by the U.S. Citizenship and Immigration Services. Learn more about the E-Verify program.


Disclaimer

This job description is intended to provide a general overview of the duties and responsibilities of the position. It is not exhaustive and does not include every task that may be required. Duties and responsibilities may change over time, and additional tasks may be assigned as needed. Zepto reserves the right to add, remove, or modify duties at the discretion of the company or its managers.


Recruitment Notice

At Zepto Life Technology, we value direct connections with our candidates. We do not accept resumes from external staffing agencies or independent recruiters for any of our openings unless there is a signed agreement with HR for the specific position. Please note that Zepto Life Technology will not pay fees for unsolicited submissions.