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Medical Device Software Engineer Jobs (NOW HIRING)

Intuvie

Senior SQA Engineer

Natick, MA · On-site

$120K - $130K/yr

Senior SQA Engineer Department: Product Development Reports To: Principal SQA Engineer/Tech Lead ... Develop solid understanding of the medical device software products * Document testing ...

Intuvie

Senior SQA Engineer

Natick, MA · On-site

$120K - $130K/yr

Senior SQA Engineer Department: Product Development Reports To: Principal SQA Engineer/Tech Lead ... Develop solid understanding of the medical device software products * Document testing ...

Cesna Group

Senior Software Engineer

San Diego, CA · On-site

$100K - $200K/yr

We are seeking a Senior Software Engineer to play a key role in maintaining, evolving, and ... As medical device development is iterative and subject to regulatory, technical, and business ...

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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.

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Medical Device Software Engineer jobs near you

Senior SQA Engineer

Intuvie

Natick, MA • On-site

$120K - $130K/yr

Full-time

Posted 25 days ago

Job description

Position Title: Senior SQA Engineer Department: Product Development


Reports To: Principal SQA Engineer/Tech Lead FLSA: exempt

GENERAL SUMMARY

Senior SQA Engineer is a senior-level position that involves the testing and verification of complex software solutions to ensure they meet quality standards. This role identifies software defects and contributes to the delivery of high-quality products that meet the needs of the intended use of our products as well as the quality and regulatory expectations for medical device development and production.


ESSENTIAL JOB FUNCTIONS

  • Participate in verification, testing, and documentation of medical device software per governing SOPs
  • Document verification procedures, verification results and traceability matrices.
  • Develop solid understanding of the medical device software products
  • Document testing methodologies, along with defect tracking and reporting.
  • Create, execute, and maintain test scripts for use within projects and regression testing.
  • Set up and maintain testing environments for different testing needs
  • Work closely with the software engineering team in all phases of the development cycle.
  • May work on automating verification procedures to achieve test automation of the medical device software products
  • Mentor more junior SQA engineers and conduct technical training for the SQA engineering team.
OTHER DUTIES AND RESPONSIBILITIES
  • Additional responsibilities may or may not be assigned to the employee; role assignment will be reviewed on a case-by-case basis determinant upon individual strengths, experience, knowledge, and expertise.


PREPARATION, KNOWLEDGE, SKILLS & ABILITIES
  • 5-10 years of experience with a bachelor’s degree, 3-7 years of experience with a master’s degree, or 1-5 years of experience with a PhD degree in mathematics, computer science, engineering, or related field from a 4-year college or university.
  • 3-5 years’ experience in software testing of medical device software.
  • Strong understanding of test automation is a plus.
  • Good testing knowledge and experience of software applications.
  • Good knowledge of QA process development and testing experience with software that has a hardware component is a plus.
  • A strong sense of software quality and attention to details.
  • Excellent written and verbal communication skills.
  • Strong analytical problem solving skills.
  • Ability to mentor staff
  • Ability to work successfully in various sizes of teams or independently to meet project deadlines.