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Biomedical Engineer Medical Devices Jobs (NOW HIRING)

Novel Microdevices

Biomedical Engineer

Baltimore, MD · On-site

Job Title: Biomedical Engineer Location: 101 W Dickman St, Suite 300, Baltimore, MD 21230 ... Medical Devices (IVD preferred) * Familiarity with FDA design controls, ISO 13485, and risk ...

Hemostasis, LLC

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Chemical Engineer - Medical Devices

White Bear Lake, MN · On-site

$90K - $120K/yr

Chemical Engineer - Medical Devices Hemostasis, LLC designs, develops, manufactures, and markets advanced hemostatic technologies for use in the medical device industry. We are seeking a hands-on ...

Guidehouse

Biomedical Engineer

Rockville, MD

$65K - $108K/yr

Medical Data Analyst & Researcher Travel Required: None Clearance Required: Ability to Obtain ... Provide technical expertise in the use of special devices and equipment, enhancing the productivity ...

Guidehouse

Biomedical Engineer

Rockville, MD

$65K - $108K/yr

Medical Data Analyst & Researcher Travel Required: None Clearance Required: Ability to Obtain ... Fabricate special purpose devices for clinical and research applications. * Manufacture and repair ...

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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 Jun 8, 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.

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 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:
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What job categories do people searching Biomedical Engineer Medical Devices jobs look for? The top searched job categories for Biomedical Engineer Medical Devices jobs are:
Biomedical Engineer Medical Devices jobs near you
Infographic showing various Biomedical Engineer Medical Devices job openings in the United States as of May 2026, with employment types broken down into 100% Full Time. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $94,807 per year, or $45.6 per hour.
Biomedical Engineer

Biomedical Engineer

Novel Microdevices

Baltimore, MD • On-site

Full-time

Posted 10 days ago

Job description

Job Title: Biomedical Engineer
Location: 101 W Dickman St, Suite 300, Baltimore, MD 21230
Employment Type: Full-time
About Novel Microdevices:
Novel Microdevices is redefining point-of-care diagnostics with cutting-edge diagnostics products designed for rapid, reliable, and actionable medical insights. Our team is building next-generation diagnostic platforms using embedded systems, real-time image processing, and cloud-integrated data solutions to empower healthcare professionals worldwide.
Job Summary:
We are looking for a highly motivated and detail-oriented Engineer to lead testing and verification efforts for the Novel Dx device.
In this role, you will operate at the interface of Systems Engineering, integration of mechanical engineering and biochemistry on a complex electromechanical device. You will be supporting a senior biomedical engineer in developing calibration protocols for manufacturing and driving Clinical Verification and Validation (V&V) activities. You will execute test strategies to ensure the device consistently meets performance and regulatory requirements. This role requires excellent manual dexterity, a commitment to quality, and the ability to work efficiently in a fast-paced environment.
Key Responsibilities:
Device Assembly and Hands-on testing support
  • Operate basic mechanical assembly tools to support routine instruments and subassembly builds.
  • Perform assembly activities in accordance with approved SOPs, work instructions, and established procedures.
  • Develop new SOPs and revise existing procedures to document assembly methods, process improvements, and best practices.
  • Define and document acceptance and rejection criteria for instruments, components, and subassemblies.
  • Build working expertise in instrument subassemblies, including their functions, interfaces, and impact on overall system performance.
  • Provide day-to-day hands-on support to the testing team, including making on-demand changes to instrument control parameters as needed during test execution.
  • Investigate, document, and communicate defects, working with all stakeholders in the team to drive timely resolution and prevent recurrence.
  • Develop foundational wet lab skills to support testing, sample handling, and related laboratory activities.
  • Support Corrective and Preventive Actions (CAPA) investigations and documentation arising from V&V activities

Software Development and Support
  • Investigate unexpected events, issues, or software bugs. Collaborate in cross-functional teams to trouble-shoot complex system-level field complaints. Report to team leadership on investigation outcome and recommend test plan. Verify fixes.
  • Complete software testing and activities for development of user stories.
  • Perform exploratory testing, system level end to end testing, develop test datasets and execute automation scripts (to ensure application software releases are of high quality). Evaluate test cases for automation suitability and execute conversion as required.
  • Maintain documentation and support other team members to maintain Design History Files (DHF) in compliance with FDA 21 CFR 820 and applicable standards for 510(k) submissions.

Calibration, Manufacturing Transfer & Process Development
  • Work towards development of calibration and validate calibration procedures for instruments and subsystems
  • Ensure calibration processes are robust, repeatable, and transferable to manufacturing technicians.
  • Define and document acceptance/rejection criteria for instruments and subassemblies
  • Provide training and documentation to support manufacturing and quality teams
  • Support design transfer activities, ensuring smooth transition from development to production.

Required Qualifications:
  • Background in biomedical, systems, or electrical/mechanical engineering which translates into cross functional ability to work with electronics/firmware and able to understand biological systems to run assays on a microfluidic device and interpret the data
  • 2+ years of relevant industry experience working with Medical Devices (IVD preferred)
  • Familiarity with FDA design controls, ISO 13485, and risk management standards
  • Strong systems thinking and communication skills to work across hardware, software, and biological interfaces

Compensation and Benefits:
  • Bi-weekly pay schedule.
  • Eligible for the Company's Employee Stock Option Incentive Plan.
  • Access to standard benefits package including healthcare and other company-offered plans.

Additional Information:
  • Employment is at-will.
  • Role is in-person and due to the nature of the work, it cannot be supported adequately from a remote location
  • Must be authorized to work in the United States.

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