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Research Development Medical Device Engineer Jobs

Medical Device Engineer I

Rochester, NY · On-site

$65K - $100K/yr

We have a significant global research, development, manufacturing and commercial footprint of ... The Medical Device Engineer II supports the design and development of contact lenses within Bausch ...

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 ...

$65K - $100K/yr

We have a significant global research, development, manufacturing and commercial footprint of ... The Medical Device Engineer II supports the design and development of contact lenses within Bausch ...

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 ...

... days, Medical, Dental and Vision insurance, 401K retirement savings plan, Life Insurance ... Evaluate and integrate relevant engineering advances for improving or solving problems Understand ...

... medical device company in the Twin Cities is seeking a Director of Research & Development to lead ... This critical leadership role will oversee a team of approximately 30 engineers, with a strong ...

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.

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Research Development Medical Device Engineer information

See salary details

$20K

$96.6K

$151K

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

As of Jun 29, 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:
What states have the most Research Development Medical Device Engineer jobs? States with the most job openings for Research Development Medical Device Engineer jobs include:
Infographic showing various Research Development Medical Device Engineer job openings in the United States as of June 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.
Senior Device Engineer, Pharmaceutical R&D

Senior Device Engineer, Pharmaceutical R&D

Transpire BIO Inc.

Weston, FL • On-site

$99K - $136K/yr

Full-time

Posted 16 days ago


Job description

Position Summary
The Senior Device Engineer is responsible for device engineering activities in the context of pharmaceutical research and development (R&D). The device mechanical engineer will be responsible for early to late-stage device development activities and commercialization of drug-device combination products. The Device engineer will be responsible for design, prototyping, technical analysis, and testing of orally inhaled and nasal drug products (OINDPs). Provide device engineering leadership in the direction, initiation, planning, coordination, implementation, execution, control, and completion of specific device project(s) ensuring consistency with organizational strategy, commitments, and goals. The device engineer will need to ensure that the device designs meet user needs, regulatory and quality requirements, and consider manufacturability. This is a hands-on position which requires daily tactical responsibilities leading up to strategic decisions.
Essential Duties and Responsibilities
  • In support of the Product Development Teams, provide technical leadership in the device development area.
  • Execute design and development of orally inhaled and nasal drug products (OINDPs) following design controls.
  • Lead and execute analysis for device and product characterization, design feasibility, and design verification.
  • Lead and execute technical analyses including statistical analysis and tolerance analysis.
  • Lead root cause investigations.
  • Support scale-up and commercialization efforts.
  • Document studies and author documents per US FDA, EMA, MHRA and other global health authority requirements.
  • Interface and lead activities with third party contract research, development, and manufacturing organizations.
  • Contribute towards and maintain device design history files (DHF).
  • Document standard operating procedures (SOPs) for design controls in the context of pharmaceutical drug-device combination products.
  • Provide project updates/reporting through program governance.
  • Provide leadership and support for inter-site best practices (technology transfer, process validation, etc.) and phase appropriate guidelines and policies.
  • Execute project strategy, priorities, and milestones ensuring visibility and accountability.
  • Proactively lead with integrity and engage cross functional project teams and stakeholders.
  • Support organizational / departmental initiatives.
  • Prepare and conduct presentations to all levels of the organization which may include project technical and budgetary information.

Required Qualifications
  • A M.S, in Mechanical Engineering, Electrical Engineering, Material Sciences or related discipline with 7 to 10 years, B.S. with 10 to 14 years device development experience in pharmaceutical or related field.
  • Experience with device development in the context of pharmaceutical R&D and product development is a must to have.
  • Must possess expert knowledge of mechanical design with preference for SolidWorks.
  • Must possess expert knowledge of tools to conduct statistical and tolerance analysis.
  • Must possess knowledge of manufacturing processes including injection molding and metal machining processes.
  • Must possess knowledge of regulations and standards including US 21 CFR Part 820, ISO 13485, ISO 14971, ISO 10993, EU MDR etc.
  • Experience with device assembly processes including manual, semi-automated and/or commercial scale automated processes is a plus.
  • Experience in development of orally inhaled and nasal drug products (OINDPs) is a plus.
  • Experience in mold tool design, optimization and qualification is a plus to have.
  • Experience with Notified Bodies and CE marking is a plus.
  • Strong English language skills including writing ability and oral communication.
  • Demonstrates good judgment as well as cultural, social, and environmental awareness.

Preferred Qualifications
  • Experience in a regulated laboratory (pharma, biotech, medical device, mechanical, or environmental)
  • Knowledge of GMP, GLP, or ISO standards

Why Join Us?
We are a fast-growing pharmaceutical startup dedicated to innovation and improving patient outcomes. Join us to gain hands-on experience in a growing pharmaceutical business, get exposure to various functions with opportunities for career development and work in a collaborative and supportive work environment.