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Research And Development Engineer Medical Device Jobs

Caerus Corp

Research & Development Engineer

Blaine, MN · On-site

$75K - $120K/yr

OrthoCor Medical, a division of Caerus Corp, is a rapidly growing medical device company. We are ... We are seeking a dedicated Research & Development Engineer to join our Research & Development team.

AngioSafe

Medical Device R&D Engineer

San Jose, CA · On-site

$115K - $175K/yr

Bachelor's degree in Mechanical Engineering or related engineering discipline preferred * Minimum 5 years of medical device R&D experience * Hands-on catheter prototyping and testing experience ...

CAERUS CORP

Research & Development Engineer

Blaine, MN

$75K - $120K/yr

OrthoCor Medical, a division of Caerus Corp, is a rapidly growing medical device company. We are ... We are seeking a dedicated Research & Development Engineer to join our Research & Development team.

AngioSafe

Medical Device R&D Engineer

San Jose, CA · On-site

$115K - $175K/yr

Bachelor's degree in Mechanical Engineering or related engineering discipline preferred * Minimum 5 years of medical device R&D experience * Hands-on catheter prototyping and testing experience ...

Bayer

$77K - $116K/yr

R&D Electrical Engineer - Medical Device - Indianola, PA R&D Electrical Engineer - Medical Device - Indianola, PA PURPOSE R&D Electrical Engineer - Medical Device isResponsible for the design ...

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Research And Development Engineer Medical Device information

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How much do research and development engineer medical device jobs pay per year?

As of Aug 1, 2026, the average yearly pay for research and development engineer medical device in the United States is $96,571.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,500.00 and $117,000.00 per year, depending on experience, location, and employer.

What does a Research and Development Engineer do in the medical device industry?

A Research and Development (R&D) Engineer in the medical device industry is responsible for designing, developing, and testing new medical devices and technologies. They work closely with cross-functional teams to ensure products meet regulatory standards, are safe for patient use, and address clinical needs. Their tasks may include prototyping, conducting experiments, analyzing data, and collaborating with manufacturing teams to bring products from concept to market. R&D Engineers also stay updated on technological advancements and regulatory changes to ensure innovation and compliance.

What is the difference between Research And Development Engineer Medical Device vs Quality Assurance Engineer Medical Device?

AspectResearch And Development Engineer Medical DeviceQuality Assurance Engineer Medical Device
Primary FocusDesigning, developing, and testing new medical device productsEnsuring products meet quality standards and regulatory requirements
Required CredentialsEngineering degree, knowledge of product developmentEngineering or science degree, knowledge of quality systems
Work EnvironmentResearch labs, product development teamsManufacturing facilities, quality control departments
Industry UsageInvolved in innovation and product creationInvolved in compliance, validation, and process improvement

While both roles require engineering knowledge and are integral to the medical device industry, Research And Development Engineers focus on creating and testing new products, whereas Quality Assurance Engineers ensure these products meet safety and quality standards throughout production.

What are some common challenges faced by Research and Development Engineers in the medical device industry?

Research and Development Engineers in the medical device industry often face challenges such as navigating complex regulatory requirements, managing tight project timelines while ensuring product safety and efficacy, and collaborating with cross-functional teams like quality assurance and clinical affairs. Additionally, adapting to rapid technological advancements and integrating feedback from clinicians and end-users into the design process can be demanding. These challenges require strong problem-solving skills, adaptability, and effective communication to deliver innovative and compliant medical devices.

What are the key skills and qualifications needed to thrive as a Research and Development Engineer in Medical Devices, and why are they important?

To excel as a Research and Development Engineer in Medical Devices, you need a solid background in biomedical engineering or a related field, strong problem-solving skills, and experience with product development cycles. Familiarity with CAD software, prototyping tools, regulatory standards like ISO 13485, and relevant certifications (such as Six Sigma) is highly valued. Excellent teamwork, creativity, and effective communication are crucial soft skills for collaborating across multidisciplinary teams and driving innovation. These competencies ensure the design and launch of safe, effective, and compliant medical devices that improve patient outcomes.
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What cities are hiring for Research And Development Engineer Medical Device jobs? Cities with the most Research And Development Engineer Medical Device job openings:
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Research And Development Engineer Medical Device jobs near you
Infographic showing various Research And Development Engineer Medical Device job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 73% Full Time, 20% Part Time, and 6% Contract. Highlights an 93% Physical, 1% Hybrid, and 6% Remote job distribution, with an average salary of $96,571 per year, or $46.4 per hour.

Product development Engineer(Medical device)

Intellectt INC

Foxboro, MA • On-site

Contractor

Re-posted 4 days ago

Job description

Role : Product development Engineer
Location:Mansfield, MA 
 
Job description:

  • Contribute to medical device product development and sustaining activities

  • Draft test protocols, perform data analysis, and ensure traceability to requirements

  • Participate in design verification & validation (V&V) efforts

  • Support EUMDR remediation projects and update technical documentation

  • Collaborate with cross-functional teams to ensure compliance with regulatory standards

  • Work with technical files, risk management documentation, and design history files (DHF)

Must-Have Qualifications:

  • Bachelor’s degree in Engineering (Mechanical or Biomedical preferred)

  • 5+ years of medical device industry experience

  • 3+ years in product development or R&D

  • Strong understanding of design controls, V&V process, and traceability