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How much do medical device phd jobs pay per hour?

As of Jun 8, 2026, the average hourly pay for medical device phd 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 are some common challenges faced by PhDs working in the medical device industry, and how can they be addressed?

PhDs entering the medical device industry often encounter challenges such as adapting to the fast-paced product development cycle, working within regulatory frameworks, and translating academic research into practical solutions. Success in this role requires strong communication skills to collaborate with cross-functional teams like engineering, marketing, and regulatory affairs. Building familiarity with industry standards (e.g., ISO 13485, FDA regulations) and gaining hands-on experience with project management can help address these challenges and ensure a smooth transition from academia to industry.

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

To thrive as a Medical Device PhD, you need a doctoral degree in biomedical engineering or a related field, with expertise in medical device design, development, and regulatory standards. Familiarity with technical tools such as CAD software, statistical analysis programs, and knowledge of FDA or CE regulatory processes is crucial. Strong problem-solving, communication, and project management skills set top candidates apart in multidisciplinary teams. These skills enable the successful creation, testing, and approval of innovative medical devices that meet safety and efficacy standards.

What is a Medical Device PhD?

A Medical Device PhD is an individual who has earned a Doctorate (PhD) with a focus on medical devices, typically through research in biomedical engineering, materials science, or a related field. These professionals are experts in designing, developing, and testing medical technologies used for diagnosis, treatment, or monitoring of health conditions. They may work in academic research, the medical device industry, regulatory agencies, or clinical settings, contributing to the innovation and safety of medical products. Their work often involves multidisciplinary collaboration and advanced knowledge of engineering, biology, and regulatory standards.

What is the difference between Medical Device Phd vs Medical Device Engineer?

AspectMedical Device PhdMedical Device Engineer
Required CredentialsPhD in relevant field, research experienceBachelor's or Master's in engineering or related field
Work EnvironmentResearch labs, development teams, academiaDesign, testing, manufacturing settings
Employer & Industry UsageUniversities, research institutions, R&D departmentsMedical device companies, manufacturing firms
Common Search & ComparisonYesYes

The Medical Device Phd typically focuses on research, development, and innovation in medical devices, often working in labs or academia. In contrast, Medical Device Engineers are more involved in designing, testing, and manufacturing medical devices in industry settings. Both roles require technical knowledge, but their daily tasks and work environments differ significantly.

More about Medical Device Phd jobs
What cities are hiring for Medical Device Phd jobs? Cities with the most Medical Device Phd job openings:
What states have the most Medical Device Phd jobs? States with the most job openings for Medical Device Phd jobs include:
What job categories do people searching Medical Device Phd jobs look for? The top searched job categories for Medical Device Phd jobs are:
Medical Device Phd jobs near you

Veterinary Medical SME

Tunnell Government Services

Bethesda, MD • On-site

Full-time

Posted 23 days ago

Job description

Tunnell Government Services, Inc., is comprised of the industry's leading scientists, medical and technical experts, and human capital and organizational development professionals. We approach all projects as a team and are committed to helping our clients transform and quickly achieve strategic goals. If you are interested in joining an employee-owned company that develops and implements innovative, integrated and differentiated solutions, please click on the links below to find the job that is right for you and contact us.
FDA Veterinary Medical SME Position Description
The successful candidate will serve as a clinical and technical authority to a variety of internal and external stakeholders regarding an array of medical and radiological health products. They will provide scientific, technical, product development, and product validation advice as part of research protocol review, assessment of technical data included in regulatory submissions, as relevant to regulatory review of medical devices. Such submissions include Premarket Notification (510(k)), Premarket Approval Application (PMA), etc.
Qualifications
  • The candidate must possess a Doctor of Veterinary Medicine (DVM) degree or equivalent, and an unrestricted license to practice veterinary medicine in a state or territory of the United States.
  • Additional advanced degrees (MS, PhD) or Board certifications in a related/applicable field are strongly preferred.
  • 7 years of experience is required (clinical, academic, and/or industry experience)
  • General knowledge and experience with a variety of medical device development technical disciplines
  • Exceptionally strong written and verbal communication skills
  • Ability to communicate well with others using excellent written and verbal communication skills.
  • Excellent interpersonal skills, with the ability to effectively work both independently and within a team of technical personnel.
  • Proficiency with Microsoft Office Suite (Outlook, Word, Excel, etc.)

Responsibilities
  • The contractor shall provide expert consultant service in the area of Veterinary Medicine and use of animal models as related to Human Medical Device Regulatory Review, consistent with (but not limited to) the following consensus standards:
    • FDA "Guidance for Industry and Food and Drug Administration Staff" documents and webinars, applicable to animal use and/or medical devices, such as General Considerations for Animal Studies for Medical Devices Draft Guidance for 4 Industry and Food and Drug Administration Staff - DRAFT GUIDANCE (October 14, 2015) LINK and Requests for Feedback on Medical Device Submissions: The Pre-Submission Program and Meetings with Food and Drug Administration Staff
      • Applicable international or other consensus standards relevant to medical device evaluation within biological systems, such as "Use of International Standard ISO 10993-1, "Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process" dated September 4, 2020.
      • Consensus sources within the discipline of veterinary medicine, which define standards and best practices for use of animals within applicable research settings, such as the National Research Council Guide for the Care and Use of Laboratory Animals, 8th edition, and the Guide for the Care and Use of Agricultural Animals in Research and Teaching
  • Provide expert consultation services to OHT review teams in support of medical device reviews, specifically applying expertise in the planning, conduct and review of animal studies used to validate the feasibility, safety and/or efficacy of medical devices. These aspects are directly relevant to the medical device design validation and hazard assessment process.
  • Participate in meetings to discuss these device submissions with both internal and external sponsors
  • Write reviews and assist with development of other documents as needed
  • Assist OHT staff as needed with projects in OPEQ's OHTs including but not limited to:
    • Assist with conducting interviews
    • Attending meetings
    • Data analysis
    • Communications with internal and external stakeholders
    • Assist with writing drafts of internal and external communication

Job Type: Full Time Employee
Schedule: Monday through Friday (No Holidays)
Location: This position is 100% telework.
Must be a US Citizen or a Full Green Card holder.
Tunnell strives to hire and retain the most qualified talent. We believe that having employees with different backgrounds and capabilities contributes to the success of our business. To attract qualified applicants, Tunnell posts to a wide variety of job sites. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Please be advised that certain client contracts may outline specific requirements for onsite work. Tunnell employees and/or contractors are expected to comply with all client requirements, including any safety and health protocols.

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