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Biomedical Engineer Medical Devices Jobs (NOW HIRING)

... Biomedical Engineering , or a related engineering or science discipline. * 3+ years of relevant ... Experience in medical devices or another highly regulated industry such as aerospace, automotive ...

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As a Biomedical Engineer, you will be responsible for supporting the development, positioning ... Experience with medical devices, biomedical products, infant care medical products, or regulated ...

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Medical Devices / In-Vitro Diagnostics Travel: Local and occasional short-term business travel ... Bachelor's Degree in Electronics, Biomedical Engineering, Electrical Engineering, Medical ...

The Biomedical Engineer is responsible for overseeing small- to medium-scale healthcare technology ... Support corrective and planned maintenance activities for network-connected medical devices ...

The Biomedical / Clinical Engineer supports the planning, acquisition, implementation, and ... Provide engineering support for the lifecycle management of medical devices and clinical systems ...

The Biomedical / Clinical Engineer supports the planning, acquisition, implementation, and ... Provide engineering support for the lifecycle management of medical devices and clinical systems ...

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 ...

$35 - $41/hr

Biomedical Engineer Location: Burlington, MA, 100% Onsite Duration: 6+ months Responsibilities ... medical devices, nutritional and branded generic medicines. Working together, Abbott and Talent ...

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 ...

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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 Sep 1, 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 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.

What are the key skills and qualifications needed to thrive as a biomedical engineer in medical devices?

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 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.

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 August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $94,807 per year, or $45.6 per hour.

System Engineer - Medical Devices

Plymouth, MN โ€ข On-site

Cube Hub Inc.
Recruiting and Staffing Servicesย โ€ขย 11 - 50 employees

$40 - $50/hr

Other

This job post hasย expired today.ย Applications are no longer accepted.


Job description

System Engineer โ€“ Medical Devices

Location: Plymouth, MN 55441

Work Arrangement: Onsite

Employment Type: Contract

Pay Rate: $40โ€“$50/hour on W2

Experience Level: GC/USC preferred

Position Overview

We are seeking a System Engineer to support the technical development and lifecycle management of advanced medical devices used in critical care environments. This role will contribute to the overall technical direction of products and support activities ranging from feasibility and new product development through verification, validation, and post-market lifecycle management.

The ideal candidate will have a strong background in systems engineering, electro-mechanical product development, medical devices or other regulated industries, and requirements and risk management.

Key Responsibilities

  • Perform systems engineering activities across one or more products throughout the product lifecycle, including new product development and post-market support.
  • Understand clinical and user needs and translate them into product and system requirements.
  • Gather and manage requirements from multiple sources, including user needs, regulatory standards, human factors, quality, manufacturing, and service.
  • Support product design realization from a systems engineering perspective.
  • Develop design concepts and research methodologies to address current and future customer and business needs.
  • Create, maintain, and organize Design History File (DHF) documentation.
  • Maintain traceability between requirements, design, risk, reliability, verification, and validation activities.
  • Support product risk management and identify potential technical challenges and risk scenarios.
  • Develop and execute mitigation strategies to address technical risks and project roadblocks.
  • Investigate and resolve system-related technical issues using structured problem-solving tools such as cause-and-effect analysis and Pareto charts.
  • Perform impact assessments for proposed design, material, and process changes, as well as observations from field, service, and manufacturing environments.
  • Recommend appropriate mitigations and provide technical rationale for proposed solutions.
  • Support system integration, verification, and validation activities for medical devices.
  • Drive adherence to applicable FDA, ISO, and IEC regulations, standards, and design control procedures.
  • Collaborate with cross-functional and global teams, including engineering, quality, regulatory, manufacturing, service, and other stakeholders.
  • Manage multiple projects and priorities while delivering results according to project plans.

Required Qualifications

  • Bachelorโ€™s or Masterโ€™s degree in Electrical Engineering, Software Engineering, Mechanical Engineering, Biomedical Engineering, or a related engineering or science discipline.
  • 3+ years of relevant engineering experience.
  • Experience with systems engineering and product development.
  • Background in electro-mechanical system development.
  • Experience in medical devices or another highly regulated industry such as aerospace, automotive, or defense.
  • Understanding of software-enabled and/or internet-connected devices.
  • Knowledge of systems engineering principles, requirements management, risk management, verification, and validation.
  • Familiarity with SysML or UML.
  • Experience using requirements management tools.
  • Strong analytical, problem-solving, communication, and stakeholder management skills.
  • Ability to work independently and collaborate effectively with cross-functional, global teams.
  • Ability to manage multiple priorities and adapt to changing project needs.

Preferred Qualifications

  • Experience with medical devices used in critical care, ICU, renal care, or kidney therapy.
  • Experience with connected medical devices and/or cybersecurity.
  • Experience with DOORS and/or Jama.
  • Familiarity with Teamcenter, TrackWise8, JIRA, and ALM.
  • Knowledge of statistical methods and design/verification tools, including DOE and sample size analysis.
  • Experience with FDA, ISO, and IEC design controls and regulatory requirements.
  • Strong experience identifying technical risks, developing mitigation plans, and removing technical roadblocks.