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Remote R&D Engineer Medical Device Jobs (NOW HIRING)

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Remote Duration: 6 months + Role Summary We are looking for a Systems Engineer to serve as the ... Engineering, or a related technical discipline. โ€ข Experience in medical device development ...

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Remote Duration: 6 months + Role Summary We are looking for a Systems Engineer to serve as the ... Engineering, or a related technical discipline. โ€ข Experience in medical device development ...

Utilize technical skills to engineer innovative strategies that improve operational performance ... Responsible for facilitating the Medical Device IT Connectivity and Integration (MDICI) process by ...

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R. sales experience; credentialed (current or previous) with at least one of the following ... S. Surgitech is a growing medical device and instrument company located in Carol Stream, IL. We ...

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R. sales experience; credentialed (current or previous) with at least one of the following ... S. Surgitech is a growing medical device and instrument company located in Carol Stream, IL. We ...

The role can be remote-based or located onsite in Danvers, MA or Raritan, NJ. This role will ... performing medical device company. This is an exciting opportunity to impact development ...

The role can be remote-based or located onsite in Danvers, MA or Raritan, NJ. This role will ... performing medical device company. This is an exciting opportunity to impact development ...

This remote role is primarily based on the East Coast of the United States, with consideration for ... A bachelor's degree in engineering, sciences, or business. * Ability to work with internal teams ...

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Remote R D Engineer Medical Device information

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$37K

$106K

$142.5K

How much do remote r&d engineer medical device jobs pay per year?

As of Jun 9, 2026, the average yearly pay for remote r&d engineer medical device in the United States is $106,012.00, according to ZipRecruiter salary data. Most workers in this role earn between $104,000.00 and $104,000.00 per year, depending on experience, location, and employer.

What is the difference between Remote R&D Engineer Medical Device vs Remote Biomedical Engineer?

AspectRemote R&D Engineer Medical DeviceRemote Biomedical Engineer
Required CredentialsBachelor's or Master's in Engineering, Biomedical, or related fields; certifications varyBachelor's or Master's in Biomedical Engineering or related fields; certifications may include regulatory or clinical
Work EnvironmentPrimarily remote, collaborating with R&D teams, design, testing, and product developmentRemote or on-site, focusing on clinical applications, device integration, and research
Employer & Industry UsageMedical device companies, R&D labs, startupsHospitals, research institutions, medical device firms

The Remote R&D Engineer Medical Device and Remote Biomedical Engineer roles share similar educational backgrounds and often work in remote settings. However, the R&D engineer focuses more on product development and engineering design, while the biomedical engineer emphasizes clinical applications and research. Both roles are vital in advancing medical technology but differ in their primary focus and work environment.

What is a Remote R&D Engineer in the medical device industry?

A Remote R&D Engineer in the medical device industry is a professional who works from a location outside the traditional office or laboratory environment, focusing on the research and development of new medical devices or the improvement of existing ones. Their responsibilities typically include designing prototypes, conducting experiments, analyzing test data, and collaborating with cross-functional teams to ensure regulatory compliance and product safety. By working remotely, these engineers utilize digital tools to communicate and manage projects, allowing for flexibility while maintaining high standards of innovation and quality in medical device development.

How do Remote R&D Engineers for medical devices typically collaborate with cross-functional teams despite working offsite?

Remote R&D Engineers in the medical device industry often collaborate closely with colleagues in engineering, regulatory, quality, and clinical affairs through digital platforms. Regular video conferences, project management tools, and shared documentation systems ensure alignment across time zones and departments. Clear communication, detailed documentation, and proactive updates are essential for maintaining project momentum and meeting strict regulatory standards. While remote collaboration can be challenging initially, most organizations provide robust onboarding and support to help engineers integrate effectively with distributed teams.

What are the key skills and qualifications needed to thrive as a Remote R&D Engineer in Medical Devices, and why are they important?

To thrive as a Remote R&D Engineer in Medical Devices, you need a solid background in biomedical or mechanical engineering, product development experience, and a relevant degree such as a BS or MS. Familiarity with CAD software, regulatory standards (like FDA or ISO 13485), and prototyping tools is typically required. Strong problem-solving, collaboration, and self-motivation are vital soft skills for effective innovation and remote teamwork. These skills ensure safe, compliant, and innovative device development, even when working outside a traditional office setting.
More about Remote R D Engineer Medical Device jobs
What cities are hiring for Remote R&D Engineer Medical Device jobs? Cities with the most Remote R&D Engineer Medical Device job openings:
What are the most commonly searched types of R&D Engineer Medical Device jobs? The most popular types of R&D Engineer Medical Device jobs are:
What states have the most Remote R&D Engineer Medical Device jobs? States with the most job openings for Remote R&D Engineer Medical Device jobs include:
Infographic showing various Remote R&D Engineer Medical Device job openings in the United States as of June 2026, with employment types broken down into 25% Full Time, 25% Part Time, and 50% Contract. Highlights an 100% Remote job distribution, with an average salary of $106,012 per year, or $51 per hour.

Software Engineer/ Medical Device Development- Product Development - Remote

MILLENNIUMSOFT

San Diego, CA โ€ข On-site, Remote

Other

Posted 25 days ago


Job description

Position : Softwareย Engineer/ย Medical Device Development- Product Development - Remote

Location : San Diego, CA

Duration : 12 Months

Total Hours/week : 40.00

1st Shift

Client : Medical Devices Company

Job Category : Professional

Level of Experience : Senior Level

Employment Type : Contract on W2 (Need US Citizens or GC Holders or GC EAD or OPT or EAD or CPT)

Job Description:

  • We are seeking a highly skilled, drive, and experienced Staff Process Engineer (Software) with expertise in defining and implementing software design and development processes and design control deliverables that adhere to regulatory standards within the medical device industry.
  • This role requires a strong technical background in Software Engineering, leadership capabilities, and extensive experience in product design and development.
  • Experience in Quality and/or Systems Engineering is also a plus.
  • The engineer will play a critical role in shaping the process for defining and documenting software-centric design control elements and deliverables, as well as the software development process itself, ensuring alignment with regulatory requirements such as FDA guidance, and meeting both user and business needs.
  • They will also be remediating the design control documentation for accuracy, completeness, and clear upstream and downstream traceability from software-centric design control elements.
  • The ideal candidate will lead continuous improvement efforts, collaborate across multi-disciplinary teams, and provide technical expertise to ensure successful project outcomes.

Key Responsibilities

  • Software Process Definition: Develop and implement software processes that comply with industry standards and regulations (e.g., IEC 62304, FDA guidance, IEEE standards), with a focus on the complete software development life cycle.
  • Software Design Documentation Remediation: Develop or modify and implement software design documentation templates within the Quality Management System that comply with industry standards and regulations. Clearly demonstrate end-to-end traceability where software design control elements are included, and remediate gaps and errors as needed.
  • Leadership: Translate business and regulatory requirements into comprehensive software development processes. Conduct back testing and work collaboratively to ensure alignment with additional stakeholders, development teams, and business objectives. Maintain frequent and clear communication with team members and leaders working in all areas of the project. Identify risks and issues early on and implement mitigations as necessary.
  • Cross-Functional Collaboration: Facilitate effective knowledge sharing and collaboration across departments (e.g., Systems Engineering, Hardware Engineering, Test Engineering, Quality, and others) to resolve alignment or feasibility issues. Communicate relevant project information effectively (verbal and written) including project status, technical concepts and design details, and functional demonstrations to key internal and external stakeholders of varying technical abilities.
  • Continuous Improvement: Identify and drive opportunities for process improvement within the Software Engineering function to enhance efficiency, quality, clarity, and compliance.
  • Technical Expertise: Serve as a resource for addressing and resolving issues of process and documentation. Apply best practices from methodologies like DFSS (Design for Six Sigma) and Critical Parameter Management to all projects. Review and remediate software design control documentation.

Minimum Qualifications

Education & Experience

  • Bachelorโ€™s degree in Science or Engineering is required; a postgraduate degree is preferred
  • Minimum of 5 years of related work experience in software engineering, medical device development, or similar fields; experience with regulatory standards (e.g., IEC 62304, FDA guidance, IEEE standards) in a regulated industry is highly preferred
  • Demonstrated ability to lead multi-disciplinary engineering teams and serve as a technical leader within the organization
  • Positive attitude with an aptitude for critical thinking
  • Willingness to learn and adapt to new challenges
  • Strong organizational skills, ability to work independently and with a group
  • Ability to handle multiple tasks simultaneously and prioritize workload

Technical Skills

  • Strong background in software engineering and test, and requirements management
  • Experience in software product development, including user needs assessment, software system analysis, architectural design, integration and testing, Reliability Engineering, Project Management, and Failure Modes Effects Analysis
  • Extensive experience in the creation and maintenance of design and development documentation is preferred
  • Knowledge and experience with methodologies like DFSS or statistical test design and analysis is preferred
  • Experience in Quality engineering and design control management is a plus
  • Experience with ALM/PLM tools is a plus
  • Exceptional communication skills, both interdepartmental and cross-functional
  • Strong writing abilities and attention to detail are essential
  • Experience working in an agile development environment is a plus
  • The candidate must be legally authorized to work in the United States without limitations and require no sponsorship for visa status now or in the future (e.g. H1-B status)

This is a hybrid position. Remote work may be considered on a case-by-case basis.