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Biomedical Device Jobs (NOW HIRING)

Aptive

Biomedical Engineer / Clinical Engineer

... Device Act (SMDA), and JC requirements; ability to conduct capital asset and infrastructure ... biomedical engineering, directly supporting specialized clinical technology, including service ...

CICONIX, LLC

Research Engineer II

San Antonio, TX

Support biomedical device development, modeling and simulation systems, equipment troubleshooting, and instrumentation. * Design and validate simulation systems. * Support directed energy ...

CICONIX, LLC

Research Engineer II

San Antonio, TX · On-site

Support biomedical device development, modeling and simulation systems, equipment troubleshooting, and instrumentation. * Design and validate simulation systems. * Support directed energy ...

Aptive

... Device Act (SMDA), and JC requirements; ability to conduct capital asset and infrastructure ... biomedical engineering, directly supporting specialized clinical technology, including service ...

Abbott

Biomedical Engineer

Hartford, CT · On-site +1

Biomedical Engineer Location: Hartford, CT Duration: 12 Months Remote 80-100% travel Required ... Previous experience in a medical device company preferred * Strong organizational and follow-up ...

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Biomedical Device information

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$36.5K

$78K

$116K

How much do biomedical device jobs pay per year?

As of Jun 9, 2026, the average yearly pay for biomedical device in the United States is $78,021.00, according to ZipRecruiter salary data. Most workers in this role earn between $47,500.00 and $98,500.00 per year, depending on experience, location, and employer.

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

To thrive as a Biomedical Device Engineer, you need a strong background in biomedical engineering principles, medical device design, and regulatory compliance, typically supported by a relevant engineering degree. Familiarity with CAD software, medical device prototyping tools, and knowledge of FDA or ISO standards is essential. Strong problem-solving, teamwork, and communication skills help you collaborate with cross-functional teams and address complex design challenges. These skills ensure safe, innovative, and effective medical devices that meet both technical and regulatory requirements.

What are biomedical devices?

Biomedical devices are medical instruments or machines designed to diagnose, monitor, or treat medical conditions in humans. These devices range from simple tools like thermometers and blood pressure monitors to complex equipment such as pacemakers, MRI machines, and artificial organs. Biomedical devices play a crucial role in improving patient care, enabling accurate diagnosis, and supporting medical procedures. They must meet strict regulatory standards to ensure safety and effectiveness in healthcare settings.

What is the difference between Biomedical Device vs Biomedical Equipment Technician?

AspectBiomedical DeviceBiomedical Equipment Technician
CredentialsTypically requires a degree in biomedical engineering or related fieldOften holds certifications like CBET or associate degree in biomedical technology
Work EnvironmentDesign, develop, and test medical devices in labs or manufacturing settingsInstall, maintain, and repair medical equipment in hospitals or clinics
Industry UsageUsed in research, development, and manufacturing of medical devicesPrimarily employed in healthcare facilities for equipment management

While both roles involve medical technology, Biomedical Device professionals focus on designing and developing medical devices, whereas Biomedical Equipment Technicians specialize in maintaining and repairing existing medical equipment in healthcare settings.

What are some typical challenges faced by professionals working in biomedical device roles, and how can they be addressed?

Professionals in biomedical device roles often encounter challenges such as strict regulatory compliance, rapid technological changes, and the need for interdisciplinary collaboration. Navigating complex FDA or international regulations requires attention to detail and frequent communication with regulatory teams. Staying updated on emerging technologies and best practices is essential, as is working effectively with engineers, clinicians, and manufacturing teams. Proactively seeking professional development and fostering open communication within cross-functional teams can help address these challenges.
More about Biomedical Device jobs
What cities are hiring for Biomedical Device jobs? Cities with the most Biomedical Device job openings:
What are the most commonly searched types of Biomedical Device jobs? The most popular types of Biomedical Device jobs are:
What states have the most Biomedical Device jobs? States with the most job openings for Biomedical Device jobs include:
What job categories do people searching Biomedical Device jobs look for? The top searched job categories for Biomedical Device jobs are:
Biomedical Device jobs near you
Infographic showing various Biomedical Device job openings in the United States as of June 2026, with employment types broken down into 92% Full Time, 3% Part Time, and 5% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $78,021 per year, or $37.5 per hour.

Biomedical Engineer

Tunnell Government Services

Washington, DC • On-site

Full-time

Posted 12 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.

Biomedical Engineer SME Position Description

The successful candidate will be a Biomedical Engineer, with broad experience in aspects of the discipline that are relevant to the medical device domain, e.g., design, development, refinement, etc. 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. Such submissions include Premarket Notification (510(k)), Premarket Approval Application (PMA), etc.

The candidate should have demonstrated at the interface of advanced engineering and clinical medicine. Expertise in areas of research and development, quality and regulatory affairs, manufacturing and production, and clinical evaluation and field support should be evident. Additional specialization in relevant areas, such as biomaterials, biomechanics, bioinstrumentation, is desired.

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).

Qualifications

  • The candidate must possess a bachelor's degree (BS) in biomedical engineering.
  • An advanced degree (MS, PhD) in a related/applicable field is strongly preferred.
  • 10 years of experience is required
  • Experience with directly supporting FDA 510(k) and related regulatory submissions is preferred
  • 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 devices relative to regulatory and technical aspects of biomedical engineering.
  • 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

Must be a US Citizen or Full Green Card holder.

Job Type: Full Time Employee

Schedule: Monday through Friday (No Holidays)

Location: This position is 100% telework.

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.