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Medical Device Phd Jobs (NOW HIRING)

BSI Group

Medical Device QMS Auditor

Concord, NC · Remote

$98K - $123K/yr

Job Title: Medical Device QMS Auditor Location: Candidates must reside in one of the following ... Advanced degree (MS, PhD) in engineering, science, or related technical discipline preferred. The ...

Mizuho OSI

Systems Engineer, Medical Device

Union City, CA · On-site

$82K - $150K/yr

... medical device development projects starting from technology exploration, product definition, to ... Bachelor's Degree in Engineering or related field 1-8 YOE, Master's degree 1-3 YOE, PhD 1+ years of ...

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How much do medical device phd jobs pay per hour?

As of Sep 1, 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 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 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 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 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.

What can I do with a medical device PhD?

A medical device PhD prepares individuals for research, development, and regulatory roles in the medical device industry. Graduates can work in product design, clinical evaluation, quality assurance, or regulatory affairs, often utilizing skills in biomedical engineering, data analysis, and medical sciences. These roles are typically found in healthcare companies, research institutions, or regulatory agencies.
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Medical Device Phd jobs near you
Infographic showing various Medical Device Phd job openings in the United States as of August 2026, with employment types broken down into 25% Full Time, and 75% Contract. Highlights an 87% In-person, and 13% Remote job distribution, with an average salary of $103,662 per year, or $49.8 per hour.

Medical Device Engineer or Materials Scientist (Implantable Device Degradation)

Tunnell Government Services

Bethesda, MD • On-site

Full-time

Posted 22 days ago

Job description

Medical Device Engineer or Materials Scientist (Implantable Device Degradation) SME Position Description - 12 Month Term Position 

The successful candidate will be either an Engineer (Biomedical, Chemical, Mechanical) or Materials Scientist and Medical Device subject matter expert, with extensive experience involving degradation (fretting, wear, and corrosion) of implantable medical devices.

They will provide scientific, technical, product development, product validation, and sustaining engineering advice as part of regulatory review of medical devices, with specific attention to premarket submissions that include mechanical functions. Such submissions include Premarket Notification (510(k)), Premarket Approval Application (PMA), etc.

The candidate should possess expertise and/or direct experience enabling the competent analysis of key components of the regulatory approach to assess device risk to a patient, a user of a device, or others in the environment of use. These include, but are not limited to analysis of aspects such as device design and modeling, analysis and simulation, material selection, prototyping and testing, manufacturing, documentation, and human factors/ergonomics.

The candidate should be familiar with applicable industry standards and regulatory requirements, such as, but not limited to, FDA Guidances (Appropriate Use of Voluntary Consensus Standards in Premarket Submissions for Medical Devices), US regulatory standards (21 CFR Part 820 -- Quality System Regulation), and ANSI standards (ANSI/AAMI/ISO 14971: Medical devices - Applications of risk management to medical devices).

The candidate should also possess expertise, and/or direct experience enabling them to act as a subject matter expert on matters pertaining to medical device basic safety and essential performance.  The candidate should also have experience involving the design and analysis of medical device systems, and performance of, and interpretation of results produced through standardized device testing approaches, in support of regulatory approval. The candidate should have appropriate training and experience necessary to provide effective consulting support in medical devices areas such as but not limited to shear stress evaluation, flow optimization, and standardized safety testing (i.e. ISO 10993-4). The candidate's experience should include knowledge of applicable standards, testing procedures, testing equipment, verification and validation of methods, preparation of test plans, reporting of results. 

Qualifications

  • The candidate must possess an advanced degree (MS, PhD) in in the field of Mechanical Engineering, Biomedical Engineering, Chemical Engineering, Materials Science, or equivalent.
  • The candidate must possess specific, demonstrable expertise and experience involving degradation (fretting, wear, corrosion) of implantable medical devices, preferably orthopedic and cardiovascular implants. Prior work experience and/or publications in peer-reviewed sources is necessary to demonstrate qualifications. 
  • The candidate must have experience with mechanical and chemical performance testing of orthopedic and cardiovascular medical device implants.
  • 10 years of experience is required (direct experience in medical device engineering and/or materials science)
  • General knowledge and experience with a variety of medical device development technical disciplines
  • Experience with directly supporting FDA 510(k) and related regulatory submissions
  • 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 primary focus of the role is to support analyses of medical device degradation relative to regulatory and technical aspects of mechanical/chemical engineering or materials science.
  • Provide consultation related to supporting medical device reviews (EUA, 510(k), PMA, IDE, Combination Devices, and De Novo marketing applications, Pre-submissions)
  • Participate in meetings and teleconferences; coordinate meetings with internal and external stakeholders
  • Develop written reviews and correspondence
  • Write detailed documents and reports

Job Type:  Full Time Employee

Schedule:  Monday through Friday (No Holidays)

Location:  This position is 100% telework. 

Must be US Citizen or full Green Card holder.

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