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Remote Medical Device Engineer Jobs (NOW HIRING)

Medical Device QMS Auditor

Concord, NC · Remote

$98K - $123K/yr

Technical degree (Bachelor's, or higher) in Engineering, Science, or a related technical discipline ... LI-REMOTE #LI-MS1 About Us BSI is a business improvement and standards company and for over a ...

... in a medical device industry preferred * 1+ years capital equipment sales experience preferred ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

... in a medical device industry preferred * 1+ years capital equipment sales experience preferred ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

... in a medical device industry preferred * 1+ years capital equipment sales experience preferred ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

... in a medical device industry preferred * 1+ years capital equipment sales experience preferred ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

As a trusted leader in the medical device industry, we design, manufacture, and support products that make a real difference in patient care. We believe that noninvasive technology should ultimately ...

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How much do remote medical device engineer jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for remote medical device engineer in the United States is $49.84, according to ZipRecruiter salary data. Most workers in this role earn between $35.10 and $59.62 per hour, depending on experience, location, and employer.

What is a remote medical device engineer?

A Remote Medical Device Engineer designs, develops, and tests medical devices while working from a remote location. They ensure compliance with industry regulations and collaborate with cross-functional teams to improve device functionality and safety. Responsibilities may include CAD modeling, prototyping, software integration, and regulatory documentation. Remote engineers use digital tools to communicate with teams and manage development processes efficiently. Strong technical expertise and knowledge of medical device regulations are essential for this role.

What is a typical workday like for a remote medical device engineer?

A typical workday as a Remote Medical Device Engineer often involves designing and reviewing device components using CAD software, participating in virtual meetings to coordinate with R&D, quality assurance, and regulatory teams, and conducting documentation for regulatory submissions. You may also troubleshoot technical issues, analyze test data, and provide design updates based on feedback or test results. Regular communication with colleagues across different time zones is common, requiring flexibility and excellent organizational skills. The remote nature of the role typically offers autonomy and flexibility while maintaining close collaboration with diverse, cross-functional teams to ensure projects progress smoothly.

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

To thrive as a Remote Medical Device Engineer, you need a solid background in biomedical engineering or related fields, along with experience in product development, regulatory compliance, and device testing. Familiarity with CAD software, FDA regulations (such as 21 CFR Part 820), and risk management systems is typically required, and certifications like PMP or Six Sigma can be advantageous. Strong problem-solving abilities, effective remote communication skills, and the ability to collaborate across distributed teams are crucial soft skills. These qualifications ensure that engineers can design safe, compliant devices and contribute effectively to remote, cross-functional teams.

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Infographic showing various Remote Medical Device Engineer job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 86% Physical, 1% Hybrid, and 13% Remote job distribution, with an average salary of $103,662 per year, or $49.8 per hour.

Medical Device Cybersecurity Engineer

Remote

Meridian Bioscience, Inc.
Medical Equipment and Supplies Manufacturing • 501 - 1,000 employees

Other

Posted 11 days ago


Job description

About Meridian
Meridian Bioscience is a fully integrated life science company that develops, manufactures, markets and distributes a broad range of innovative diagnostic products. We are dedicated to developing and delivering better solutions that give answers with speed, accuracy and simplicity that are redefining the possibilities of life from discovery to diagnosis. We are looking for talented and passionate individuals that help drive our vision. Our innovative culture will allow interested candidates to discover and create, through collaboration, cutting edge solutions to tough problems.
Job Summary
The Software Engineer with a focus on Cybersecurity will play a critical part in ensuring that software integrated into our diagnostic platforms meets cybersecurity, regulatory, and quality requirements. This system-level engineering role will facilitate software development, cybersecurity testers, and regulatory functions, ensuring secure design and compliant documentation throughout the product lifecycle.
Key Duties
  • Integrate cybersecurity requirements into the design and development of software for diagnostic platforms (coding on embedded software)
  • Ensure compliance with FDA cybersecurity guidance (pre-market and post-market) and applicable North American regulations
  • Collaborate with software development teams to ensure secure-by-design implementation
  • Translate cybersecurity and regulatory requirements into clear technical specifications and documentation
  • Contribute to and maintain Design History File (DHF) documentation in compliance with design control requirements
  • Support software lifecycle activities aligned with IEC 62304
  • Participate in risk management activities in accordance with ISO 14971 (e.g., threat modeling, risk analysis, mitigation strategies)
  • Review system architecture and design to ensure alignment with secure development principles
  • Act as a cross-functional liaison between R&D, Quality, Regulatory, and Software Engineering teams
  • Other duties as assigned
  • Travel 10-15% international travel

Qualifications
  • Bachelor's or Master's degree in Software Engineering, Computer Engineering, or related field
  • 5 years of experience in software engineering or system-level roles
  • Recent experience in cybersecurity, preferably within the medical device or other regulated industry
  • Strong understanding of:
    • FDA cybersecurity guidance (pre-market and post-market)
    • IEC 62304 software lifecycle processes
    • ISO 14971 risk management principles
  • Experience working with regulated design documentation (e.g., DHF, technical files)
  • Ability to interpret and communicate complex technical and regulatory requirements across multidisciplinary teams
  • Experience with Software and Hardware integration
  • Strong collaboration and stakeholder communication skills
  • Experience with threat modeling, vulnerability assessment, or security risk management
  • Preferred :
  • Experience as a Software Lead or Technical Lead capacity
  • Familiarity with Laboratory Information Systems (LIS) and remote device management (IoT)
  • Knowledge of additional standards and best practices, such as:
  • AAMI TIR57 / TIR97 (Medical device Cybersecurity)
  • IEC 81001-5-1 (secure product development lifecycle)
  • Exposure to secure development frameworks (e.g., NIST Cybersecurity Framework, OWASP)
  • Basic knowledge of French or Korean language

*All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status. (USA Only)*