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Remote Medical Device Software Engineer Jobs (NOW HIRING)

Collaborate with product development, quality, clinical, and engineering teams to ensure regulatory compliance * Interpret FDA guidance related to medical device software and digital health ...

Senior DevOps Engineer

Rochester, NY · Remote

$128K - $164K/yr

... medical device software. The DevOps Engineer will partner closely with Software, Systems, and ... This position is remote eligible but candidates local to Rochester, NY are highly desirable. NOTE:

Senior DevOps Engineer

Rochester, NY · Remote

$128K - $164K/yr

... medical device software. The DevOps Engineer will partner closely with Software, Systems, and ... This position is remote eligible but candidates local to Rochester, NY are highly desirable. NOTE:

Experience working within HIPAA and medical device software development environments ... Fully remote work environment with virtual events and yearly retreats, because we like to have fun ...

Medical Device QMS Auditor

Concord, NC · Remote

$98K - $123K/yr

Technical degree (Bachelor's, or higher) in Engineering, Science, or a related technical discipline ... Hands-on experience with software-controlled medical devices, SaMD, or automated manufacturing ...

IoT / Edge Software Engineer

MD · Remote

$68K - $141K/yr

Develop and maintain secure device authentication, data encryption, and remote firmware update ... This position is eligible for company benefits including medical, dental, and vision insurance with ...

IoT / Edge Software Engineer

Bethesda, MD · On-site +1

$68K - $141K/yr

Develop and maintain secure device authentication, data encryption, and remote firmware update ... This position is eligible for company benefits including medical, dental, and vision insurance with ...

Software Engineer, On Device

Ann Arbor, MI · Remote

$120K - $150K/yr

... remote work. Our Commitments: Utilidata values the diversity of our team. We provide equal ... medical condition, pregnancy or childbirth, sexual orientation, genetics, genetic information ...

Software Engineer, On Device

Ann Arbor, MI · On-site +1

$120K - $150K/yr

... remote work. Our Commitments: Utilidata values the diversity of our team. We provide equal ... medical condition, pregnancy or childbirth, sexual orientation, genetics, genetic information ...

Showing results 41-60

Remote Medical Device Software Engineer information

See salary details

$63.5K

$147.5K

$205.5K

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

As of Aug 24, 2026, the average yearly pay for remote 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 does a remote medical device software engineer do?

A Remote Medical Device Software Engineer designs, develops, tests, and maintains software used in medical devices while working from a remote location. They are responsible for ensuring the software complies with healthcare regulations and safety standards, such as FDA or ISO requirements. Their work often involves collaborating with cross-functional teams, troubleshooting issues, and updating software throughout the product lifecycle. This role requires expertise in both software engineering and medical device regulations.

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

To thrive as a Remote Medical Device Software Engineer, you need strong programming skills (especially in C/C++ or Python), a solid understanding of embedded systems, and a degree in computer science, biomedical engineering, or a related field. Familiarity with medical device standards (such as IEC 62304), version control systems like Git, and experience with software validation and regulatory documentation are typically required. Excellent problem-solving abilities, proactive communication, and strong collaboration skills are vital for working effectively in distributed teams. These skills ensure the development of safe, high-quality software that meets strict regulatory requirements and supports patient health.

What are some common challenges faced by remote medical device software engineers, and how can they be addressed?

Remote Medical Device Software Engineers often encounter challenges related to stringent regulatory compliance, secure communication, and effective collaboration with cross-functional teams such as QA, hardware engineers, and clinicians. Managing time zones and clear documentation is essential to ensure code quality and traceability, especially since these devices directly impact patient safety. To address these challenges, engineers should prioritize robust version control, frequent virtual check-ins, and proactive communication to align with team goals and regulatory requirements. Leveraging collaboration tools and maintaining detailed documentation can further streamline the development process and facilitate smooth teamwork.
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Cities with the most Remote Medical Device Software Engineer job openings:

What are the most commonly searched types of Medical Device Software Engineer jobs?

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

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Infographic showing various Remote Medical Device Software Engineer job openings in the United States as of August 2026, with employment types broken down into 73% Full Time, 15% Part Time, and 12% Contract. Highlights an 4% In-person, and 96% Remote job distribution, with an average salary of $147,524 per year, or $70.9 per hour.

Regulatory Affairs Manager-US

Remote

Full-time

Re-posted 15 days ago


Job description

Symmetrio is recruiting for our client for a Regulatory Affairs Manager to lead U.S. regulatory strategy and submissions for innovative healthcare software products. This role will focus on FDA 510(k) submissions and regulatory pathways for Software as a Medical Device (SaMD) within a global, multinational environment.
Key Responsibilities
  • Lead preparation and submission of FDA 510(k) filings for healthcare software and digital health products
  • Develop and execute regulatory strategies supporting product development and commercialization
  • Collaborate with product development, quality, clinical, and engineering teams to ensure regulatory compliance
  • Interpret FDA guidance related to medical device software and digital health technologies
  • Partner with global regulatory teams to support international regulatory initiatives

Requirements
  • 5-10+ years of regulatory affairs experience in medical devices or healthcare software
  • Proven experience with FDA 510(k) submissions, ideally for software-based medical devices
  • Strong knowledge of SaMD, FDA regulations, and quality standards (21 CFR Part 820, ISO 13485, IEC 62304)
  • Experience working within a multinational organization
  • Strong cross-functional collaboration and communication skills