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Biomedical Engineer Medical Devices Jobs (NOW HIRING)

Biomedical Engineer Location: Jericho, NY Salary: $80,000 - $90,000 annually Benefits: Medical ... Basic understanding of ECG technology and related medical devices * Experience supporting health ...

Biomedical Engineer Location: Jericho, NY Salary: $80,000 - $90,000 annually Benefits: Medical ... Basic understanding of ECG technology and related medical devices * Experience supporting health ...

As a Biomedical Engineer, you will play a pivotal role in managing our medical equipment program ... Manage a recall and safety alert program for medical devices, including conducting medical device ...

We are looking for a passionate Biomedical Engineer to join our growing team and help design patient-specific medical devices and surgical solutions. In this role, you will transform medical imaging ...

As a Senior Biomedical Engineer, you will work closely with cross-functional teams in our corporate ... medical devices. Your expertise in biomechanics, human factors engineering, and device performance ...

Biomedical Engineer Sr

Falls Church, VA · On-site

$30.49 - $49.70/hr

Configures and troubleshoots medical devices for network connectivity, addressing complex ... Experience : 3 years of relevant biomedical engineering experience * Certification: Completion of 2 ...

Biomedical Engineer

Littleton, CO · On-site

$68K - $75K/yr

... patient-specific medical devices, modification of surgical splints, and meticulous data ... Join our team to apply cutting-edge biomedical engineering skills while directly impacting surgical ...

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Biomedical Engineer Medical Devices information

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$41K

$94.8K

$140K

How much do biomedical engineer medical devices jobs pay per year?

As of Jul 22, 2026, the average yearly pay for biomedical engineer medical devices in the United States is $94,807.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $116,000.00 per year, depending on experience, location, and employer.

What is the difference between Biomedical Engineer Medical Devices vs Biomedical Engineer Clinical Equipment?

AspectBiomedical Engineer Medical DevicesBiomedical Engineer Clinical Equipment
CredentialsDegree in biomedical engineering or related field, certifications like Certified Biomedical Equipment Technician (CBET)Similar credentials, often with additional focus on clinical systems
Work EnvironmentDesign, develop, and test medical devices in labs or manufacturing settingsMaintain and troubleshoot clinical equipment in hospitals or healthcare facilities
Employer & IndustryMedical device companies, manufacturing firmsHospitals, healthcare providers

Both roles require biomedical engineering degrees and certifications. Biomedical Engineer Medical Devices focuses on designing and developing new devices, while Biomedical Engineer Clinical Equipment specializes in maintaining and repairing equipment used in patient care. The roles often overlap but differ mainly in their work environment and primary responsibilities.

Do biomedical engineers work on medical devices?

Yes, biomedical engineers working in medical devices design, develop, test, and improve medical equipment such as imaging systems, prosthetics, and diagnostic tools. They often use skills in electronics, materials science, and computer programming, and may work in laboratories or manufacturing environments.

What engineers make $500,000?

Senior biomedical engineers with extensive experience, specialized skills, and leadership roles can earn salaries approaching or exceeding $500,000 annually, especially in high-demand sectors or executive positions. Achieving this level often requires advanced certifications, a strong track record, and working in competitive or high-cost regions.

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

To thrive as a Biomedical Engineer in Medical Devices, you need a solid background in biomedical engineering principles, device design, and regulatory standards, typically supported by a relevant engineering degree. Proficiency with CAD software, medical device testing tools, and a strong understanding of FDA or ISO regulations is important, and certifications like Certified Biomedical Auditor (CBA) can be advantageous. Strong problem-solving skills, attention to detail, and collaborative communication set standout professionals apart in this role. These skills and qualities are crucial for ensuring the safety, efficacy, and successful development of innovative medical devices.

What are some common challenges faced by biomedical engineers working with medical devices, and how can they be addressed?

Biomedical engineers in the medical device sector often encounter challenges such as meeting stringent regulatory requirements, ensuring device safety and reliability, and collaborating effectively with multidisciplinary teams. Navigating complex approval processes (like FDA or CE marking) requires attention to detail and up-to-date knowledge of regulations. Additionally, engineers must balance innovation with compliance, often working closely with clinicians, designers, and quality assurance professionals. Staying proactive about communication and continuous learning can help address these challenges and foster successful project outcomes.

What engineers make $300,000 a year?

Biomedical engineers specializing in medical devices can reach annual salaries of $300,000 or more, typically with extensive experience, advanced certifications, and leadership roles. High earnings are often associated with senior positions, research and development, or working in specialized or high-demand areas within the industry.

What are three jobs that a BME can work at a medical device company?

A biomedical engineer working in a medical device company can hold roles such as design engineer, responsible for developing new devices; quality assurance engineer, ensuring products meet safety standards; or regulatory affairs specialist, managing compliance with industry regulations. These positions often require knowledge of biomedical principles, engineering skills, and familiarity with industry standards and testing protocols.

What does a Biomedical Engineer in Medical Devices do?

A Biomedical Engineer specializing in medical devices designs, develops, tests, and maintains equipment used in healthcare, such as imaging machines, prosthetics, and diagnostic devices. They ensure that these devices are safe, effective, and meet regulatory standards. Their work often involves collaborating with doctors, nurses, and other engineers to create innovative solutions that improve patient care. Additionally, they may be involved in troubleshooting equipment, training medical staff on device use, and conducting research to advance medical technology.
More about Biomedical Engineer Medical Devices jobs
What cities are hiring for Biomedical Engineer Medical Devices jobs? Cities with the most Biomedical Engineer Medical Devices job openings:
What states have the most Biomedical Engineer Medical Devices jobs? States with the most job openings for Biomedical Engineer Medical Devices jobs include:
Infographic showing various Biomedical Engineer Medical Devices job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 84% Full Time, 14% Part Time, and 1% Contract. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $94,807 per year, or $45.6 per hour.
Senior Requirements Tools Engineer (Medical Devices)

Senior Requirements Tools Engineer (Medical Devices)

Intellectt INC

Pleasanton, CA • On-site

$116K - $159K/yr

Contractor

Posted 24 days ago


Job description

Job Title: Senior Requirements Tools Engineer (Medical Devices)
Location: Pleasanton, CA
Duration: 12 months
Shift Timings: 8 AM to 5 PM
Job Description:

The Requirements Tools Engineer will be responsible for enabling and supporting requirements management infrastructure for medical device product development programs. This role is focused on administering and configuring enterprise requirements management platforms, supporting data migration activities, and enabling engineering teams through processes, and training.

Working in Pleasanton, CA, this individual will collaborate with cross‑functional engineering teams to establish scalable structures and best practices that allow engineers to efficiently create and manage requirements and other design control documents in the management tool.

Responsibilities:

  • Plan and execute migration of requirements and related data from legacy tools (e.g., DOORS, Jama, Excel, Jira) into new platforms, ensuring data integrity, traceability, and compliance.
  • Administer, configure, and maintain enterprise requirements management tools, including hierarchies, templates, workflows, versioning, and baselining in alignment with the quality system.
  • Develop and maintain a requirements management plan in collaboration with cross‑functional teams, defining the overall requirements structure and links to associated design control documents.
  • Create and maintain standardized requirements templates, traceability frameworks, and governance models based on quality and regulatory requirements.
  • Maintain the requirements database, develop scripts or automation as needed, and support integrations or add‑in tools to improve usability and efficiency.
  • Provide training, documentation, and ongoing support to engineers, serving as the primary functional expert for requirements tools and best practices.

Required Qualifications:

  • Bachelor’s degree in Engineering, Computer Science, Biomedical Engineering, or a related discipline for requirements management.
  • A minimum of 5 years with hands on experience administering or configuring enterprise requirements management tools to support regulated development environments (e.g., Codebeamer, DOORS, Jama, or comparable platforms). Ability to quickly learn and adopt new tools is expected.
  • Hands‑on experience with requirements migration from legacy tools.
  • Strong understanding of medical device product development and design control principles.
  • Excellent verbal and written communication skills, with the ability to train and support engineers at all levels.
  • Ability to work effectively in a collaborative environment.
     

Preferred Qualifications:

  • Experience acting as a tool administrator, configuration owner, or advanced power user in a regulated development environment.
  • Experience defining or scaling requirements management frameworks for large or multi‑team programs.
  • Familiarity with medical device development (FDA 21 CFR Part 820) with the ability to configure tools to support compliant workflows.
  • Experience supporting software‑driven, connected, or mobile medical devices.
  • Experience with different requirements management or lifecycle tools is valued; strong foundational understanding of requirements structures and traceability is more important than experience with a specific platform.