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Research Development Medical Device Engineer Jobs

kindeva

Senior Device Engineer

Maryland Heights, MO

$101K - $138K/yr

Liaison with internal production sites, quality, regulatory R&D, and Tech Transfer/Launch Teams ... Experience in Medical Device or Combination Products Design Controls, Production, Sustaining ...

AngioSafe

Medical Device R&D Engineer

San Jose, CA

$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 ...

Dexcom

Medical Device Engineer 2

San Diego, CA · On-site

In this role you will be part of the Advanced Research and Technology team that focuses on ... Under the supervision of senior- and staff-level scientists, you will partake in the development of ...

kindeva

Senior Device Engineer

Maryland Heights, MO

$101K - $138K/yr

Liaison with internal production sites, quality, regulatory R&D, and Tech Transfer/Launch Teams ... Experience in Medical Device or Combination Products Design Controls, Production, Sustaining ...

kindeva

Senior Device Engineer

Maryland Heights, MO

$101K - $138K/yr

Liaison with internal production sites, quality, regulatory R&D, and Tech Transfer/Launch Teams ... Experience in Medical Device or Combination Products Design Controls, Production, Sustaining ...

kindeva

Senior Device Engineer

Maryland Heights, MO

$101K - $138K/yr

Liaison with internal production sites, quality, regulatory R&D, and Tech Transfer/Launch Teams ... Experience in Medical Device or Combination Products Design Controls, Production, Sustaining ...

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All JobsResearch Development Medical Device Engineer Jobs

Research Development Medical Device Engineer information

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$20K

$96.6K

$151K

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

As of Jul 21, 2026, the average yearly pay for research development medical device engineer 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 are some typical challenges faced by Research Development Medical Device Engineers when bringing a new device from concept to prototype?

Research Development Medical Device Engineers often encounter challenges such as navigating strict regulatory requirements, coordinating with cross-functional teams, and balancing innovation with manufacturability. Ensuring the device meets safety and efficacy standards while staying within budget and timeline constraints can be demanding. Additionally, effective collaboration with clinicians, quality assurance, and manufacturing teams is crucial to address technical hurdles and incorporate user feedback throughout the development process.

What does a Research Development Medical Device Engineer do?

A Research Development Medical Device Engineer is responsible for designing, developing, and testing new medical devices or improving existing ones. They work closely with cross-functional teams, including clinicians, regulatory specialists, and manufacturing engineers, to ensure that devices are safe, effective, and compliant with industry standards. Their work involves prototyping, conducting experiments, analyzing data, and documenting results throughout the product development lifecycle. Additionally, they may help navigate regulatory approval processes and support product launches.

What is the difference between Research Development Medical Device Engineer vs Product Development Engineer?

AspectResearch Development Medical Device EngineerProduct Development Engineer
CredentialsBachelor's or Master's in Engineering, Biomedical, or related fields; certifications varyBachelor's or Master's in Engineering, Mechanical, Electrical, or related fields; certifications vary
Work EnvironmentResearch labs, R&D departments, clinical settingsManufacturing, design teams, product testing facilities
Employer & Industry UsageMedical device companies, biotech firms, healthcare institutionsMedical device companies, tech firms, manufacturing industries

The Research Development Medical Device Engineer focuses on early-stage research, innovation, and prototype development of medical devices. In contrast, the Product Development Engineer emphasizes designing, testing, and refining products for manufacturing and market release. Both roles require technical expertise, but their focus and project stages differ significantly.

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

To thrive as a Research Development Medical Device Engineer, you need a strong background in biomedical engineering, mechanical or electrical engineering, and experience with product development processes, usually supported by a relevant degree. Familiarity with CAD software, prototyping tools, regulatory standards such as ISO 13485, and potentially Six Sigma or similar certifications is important. Creativity, analytical thinking, and effective teamwork skills help drive innovation and solve complex engineering challenges in multidisciplinary environments. These skills and qualifications are vital to ensure medical devices are safe, effective, and compliant with industry regulations while meeting user and market needs.
More about Research Development Medical Device Engineer jobs
What cities are hiring for Research Development Medical Device Engineer jobs? Cities with the most Research Development Medical Device Engineer job openings:
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What job categories do people searching Research Development Medical Device Engineer jobs look for? The top searched job categories for Research Development Medical Device Engineer jobs are:
Research Development Medical Device Engineer jobs near you
Infographic showing various Research Development Medical Device Engineer job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $96,571 per year, or $46.4 per hour.

Test Engineer - Verification & Validation - medical device

InnoTech Staffing

Manchester, NH • On-site

Full-time

Posted 24 days ago

Job description

InnoTECH Staffing has an immediate opening for a Test Engineer to work in a dynamic medical device R&D environment at our client who is located in Manchester, NH.

This requires being onsite 5 days a week and must be a US Citizen or Greencard holder.

Test Engineering is a high-visibility role with a significant, direct impact on the success of the project.
How you will make an impact as a Verification and Validation Test Engineer:

  • Developing and writing test procedures assessing end-to-end performance and reliability of user interfaces and hardware
  • Understanding device design and core technologies in order to inform test method development
  • Determining test coverage for revisions to design
  • Creating and evaluating test fixtures if needed for product design verification
  • Contributing to design failure investigations that may impact Risk Assessments, Hazard Analyses, and FMEAs
  • Contributing toward regulatory and agency submissions
  • Authoring Test Summaries and other documents

To be successful in this role as a Verification and Validation Test Engineer, you will need the following skills and experience:

  • Must have a BS in Physics, Biology, Electrical, Mechanical, or Biomedical Engineering.
  • Experience with research, development, and product testing
  • Experience writing procedures for others to follow
  • Experience with data and failure analysis
  • Broad measurement instrument knowledge
  • Knowledge and deep understanding of engineering fundamentals
  • Demonstrated problem solving ability and techniques
  • Ability to work as part of an interdisciplinary team
  • Self-motivated and able to self-prioritize
  • Ability to clearly explain objectives
  • Must be detail oriented and have excellent verbal and written communication skills
  • Experience in medical devices, knowledge of FDA Quality System Regulations (QSRs) and/or ISO 13485, and other medical device industry experience preferred