Flag unsafe, misleading, or overconfident biomedical engineering recommendations, especially where medical devices, patient safety, clinical workflows, biological systems, diagnostics, imaging ...
Flag unsafe, misleading, or overconfident biomedical engineering recommendations, especially where medical devices, patient safety, clinical workflows, biological systems, diagnostics, imaging ...
Flag unsafe, misleading, or overconfident biomedical engineering recommendations, especially where medical devices, patient safety, clinical workflows, biological systems, diagnostics, imaging ...
Flag unsafe, misleading, or overconfident biomedical engineering recommendations, especially where medical devices, patient safety, clinical workflows, biological systems, diagnostics, imaging ...
Flag unsafe, misleading, or overconfident biomedical engineering recommendations, especially where medical devices, patient safety, clinical workflows, biological systems, diagnostics, imaging ...
Flag unsafe, misleading, or overconfident biomedical engineering recommendations, especially where medical devices, patient safety, clinical workflows, biological systems, diagnostics, imaging ...
Flag unsafe, misleading, or overconfident biomedical engineering recommendations, especially where medical devices, patient safety, clinical workflows, biological systems, diagnostics, imaging ...
Flag unsafe, misleading, or overconfident biomedical engineering recommendations, especially where medical devices, patient safety, clinical workflows, biological systems, diagnostics, imaging ...
Flag unsafe, misleading, or overconfident biomedical engineering recommendations, especially where medical devices, patient safety, clinical workflows, biological systems, diagnostics, imaging ...
Flag unsafe, misleading, or overconfident biomedical engineering recommendations, especially where medical devices, patient safety, clinical workflows, biological systems, diagnostics, imaging ...
Flag unsafe, misleading, or overconfident biomedical engineering recommendations, especially where medical devices, patient safety, clinical workflows, biological systems, diagnostics, imaging ...
Flag unsafe, misleading, or overconfident biomedical engineering recommendations, especially where medical devices, patient safety, clinical workflows, biological systems, diagnostics, imaging ...
Flag unsafe, misleading, or overconfident biomedical engineering recommendations, especially where medical devices, patient safety, clinical workflows, biological systems, diagnostics, imaging ...
Flag unsafe, misleading, or overconfident biomedical engineering recommendations, especially where medical devices, patient safety, clinical workflows, biological systems, diagnostics, imaging ...
Flag unsafe, misleading, or overconfident biomedical engineering recommendations, especially where medical devices, patient safety, clinical workflows, biological systems, diagnostics, imaging ...
Flag unsafe, misleading, or overconfident biomedical engineering recommendations, especially where medical devices, patient safety, clinical workflows, biological systems, diagnostics, imaging ...
Flag unsafe, misleading, or overconfident biomedical engineering recommendations, especially where medical devices, patient safety, clinical workflows, biological systems, diagnostics, imaging ...
Flag unsafe, misleading, or overconfident biomedical engineering recommendations, especially where medical devices, patient safety, clinical workflows, biological systems, diagnostics, imaging ...
Biomedical Engineer
Woodlawn, MD · On-site +1
$143K - $187K/yr
As a Biomedical Engineer, GS-0858-14, you will serve as a Technical Advisor for DMEPOS technology ... medical devices and services. * Participates in the development of proposals to facilitate ...
Biomedical Engineer
Woodlawn, MD · On-site +1
$143K - $187K/yr
As a Biomedical Engineer, GS-0858-14, you will serve as a Technical Advisor for DMEPOS technology ... medical devices and services. * Participates in the development of proposals to facilitate ...
* Mechanical / Biomedical Engineer with 5 - 8 years of experience in Medical Devices. * Good knowledge on Design control and management process as per ISO 13485 and ISO 14971 * Knowledge on design ...
* Mechanical / Biomedical Engineer with 5 - 8 years of experience in Medical Devices. * Good knowledge on Design control and management process as per ISO 13485 and ISO 14971 * Knowledge on design ...
Biomedical Engineer (Sr & Jr)
Manhattan, NY · On-site
Manhattan, NY (5 days Onsite) Contract Role Summary The Senior Biomedical Engineer / Biomedical Equipment Planner will lead medical equipment planning, procurement, installation, integration ...
Biomedical Engineer (Sr & Jr)
Manhattan, NY · On-site
Manhattan, NY (5 days Onsite) Contract Role Summary The Senior Biomedical Engineer / Biomedical Equipment Planner will lead medical equipment planning, procurement, installation, integration ...
Engineer, Medical Devices (JP12014)
Thousand Oaks, CA · On-site
$37 - $41/hr
Engineer, Medical Devices (JP12014) Location: Thousand Oaks, CA. 91320 Business Unit: PFS And Lyo ... Bachelor's Degree or higher in relevant engineering or scientific field (Mechanical, Biomedical ...
Engineer, Medical Devices (JP12014)
Thousand Oaks, CA · On-site
$37 - $41/hr
Engineer, Medical Devices (JP12014) Location: Thousand Oaks, CA. 91320 Business Unit: PFS And Lyo ... Bachelor's Degree or higher in relevant engineering or scientific field (Mechanical, Biomedical ...
Medical Test Engineer
Boston, MA · On-site
... Biomedical Engineering, Software Engineering, or related field. * Minimum 5+ years of experience in Verification & Validation within Medical Devices domain. * Experience working on Cardiovascular ...
Medical Test Engineer
Boston, MA · On-site
... Biomedical Engineering, Software Engineering, or related field. * Minimum 5+ years of experience in Verification & Validation within Medical Devices domain. * Experience working on Cardiovascular ...
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 ...
Quick apply
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 ...
Senior Requirements Tools Engineer (Medical Devices)
Pleasanton, CA · On-site
$116K - $159K/yr
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 ...
Quick apply
Senior Requirements Tools Engineer (Medical Devices)
Pleasanton, CA · On-site
$116K - $159K/yr
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 ...
Biomedical Engineer
Dallas, TX · On-site
S. in Biomedical Engineering or related field. * 1-3 years medical devices and medical device development. * 1-3 years engineering calibration and preventative maintenance. * Experience in computer ...
Quick apply
Biomedical Engineer
Dallas, TX · On-site
S. in Biomedical Engineering or related field. * 1-3 years medical devices and medical device development. * 1-3 years engineering calibration and preventative maintenance. * Experience in computer ...
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 ...
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 ...
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 ...
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 ...
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 ...
Quick apply
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 ...
Biomedical Engineer Medical Devices information
See salary details
$41K - $50K
6% of jobs
$50K - $59K
12% of jobs
$59K - $68K
5% of jobs
$72.5K is the 25th percentile. Wages below this are outliers.
$68K - $77K
3% of jobs
$77K - $86K
13% of jobs
$86K - $95K
7% of jobs
The median wage is $96.5K / yr.
$95K - $104K
19% of jobs
$111.7K is the 75th percentile. Wages above this are outliers.
$104K - $113K
11% of jobs
$113K - $122K
12% of jobs
$122K - $131K
4% of jobs
$131K - $140K
7% of jobs
$41K
$94.8K
$140K
How much do biomedical engineer medical devices jobs pay per year?
As of Jun 30, 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?
| Aspect | Biomedical Engineer Medical Devices | Biomedical Engineer Clinical Equipment |
|---|---|---|
| Credentials | Degree in biomedical engineering or related field, certifications like Certified Biomedical Equipment Technician (CBET) | Similar credentials, often with additional focus on clinical systems |
| Work Environment | Design, develop, and test medical devices in labs or manufacturing settings | Maintain and troubleshoot clinical equipment in hospitals or healthcare facilities |
| Employer & Industry | Medical device companies, manufacturing firms | Hospitals, 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:
What states have the most Biomedical Engineer Medical Devices jobs? States with the most job openings for Biomedical Engineer Medical Devices jobs include:
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:
- Human Factors Engineer Medical Device
- Contract Quality Engineer Medical Device
- Manufacturing Engineer Medical
- Medical Device Development Engineer
- Mechanical Design Engineer Medical Device
- Quality Engineer Medical Device
- Salaried Vp Engineering Medical Device
- Senior Complaint Handling Medical Device
- Organon
- Biotech Consulting Internship
Full-time
This job post has expired today. Applications are no longer accepted.
Job description
Job Summary:
YO IT Consulting is a fast-growing AI Data Services company delivering training data for major AI companies. They are seeking a Biomedical Engineering Quality Assurance Lead to oversee quality and consistency across biomedical engineering AI training projects, review AI-generated content, and ensure adherence to quality standards.
Responsibilities:
• Quality monitoring: Spot-check biomedical engineering items, identify quality issues, provide ongoing feedback through DMs, and escalate recurring or critical issues.
• Technical review: Evaluate AI-generated biomedical engineering explanations, medical-device reasoning, biomechanics calculations, biomaterials discussions, bioinstrumentation workflows, biosignal explanations, diagrams/descriptions, and problem-solving steps for correctness and clarity.
• Trainer and QA communication: Update trainers and QAs on Discord about new item guidelines, project changes, workflow updates, quality expectations, and biomedical-engineering-specific review standards.
• Question handling: Respond to trainer/QA questions clearly and promptly, especially around engineering assumptions, units, formulas, biological context, device safety, regulatory considerations, standards references, and rubric interpretation.
• Trainer/QA activation management: DM contributors who are inactive or not working, encourage activation, track follow-ups, and flag availability issues when needed.
• Documentation: Create and maintain biomedical engineering project documentation, including style guides, trackers, FAQs, quality notes, examples, honeypots, calibration tasks, and onboarding materials.
• Onboarding and training: Schedule and run onboarding/training calls with trainers and QAs to explain project expectations, workflows, rubrics, quality standards, and biomedical-engineering-specific review requirements.
• Quality alignment: Ensure all trainers and QAs apply biomedical engineering guidelines consistently and understand updates as projects evolve.
• Risk and safety review: Flag unsafe, misleading, or overconfident biomedical engineering recommendations, especially where medical devices, patient safety, clinical workflows, biological systems, diagnostics, imaging, rehabilitation tools, or regulatory claims may be affected.
• Process improvement: Identify recurring quality gaps, propose workflow improvements, and help build scalable QA processes for biomedical engineering AI training projects.
Qualifications:
Required:
• Bachelor’s or Master’s degree in Biomedical Engineering, Bioengineering, Medical Engineering, Biomechanical Engineering, Electrical Engineering with biomedical focus, Mechanical Engineering with biomedical focus, or a closely related field.
• Strong grasp of the English language to follow project guidelines, communicate with teams, and provide clear technical feedback in English.
• 3+ years of professional experience in biomedical engineering, medical devices, biomechanics, biomaterials, bioinstrumentation, clinical engineering, R&D, regulatory documentation, technical review, engineering education, or related workflows.
• Strong understanding of core biomedical engineering topics such as biomechanics, biomaterials, medical devices, bioinstrumentation, biosignals, imaging systems, physiological systems, tissue engineering, rehabilitation engineering, and biomedical data analysis.
• Ability to evaluate biomedical engineering content against detailed rubrics and identify issues such as incorrect assumptions, flawed calculations, missing units, unsafe recommendations, weak biological/clinical reasoning, hallucinated standards, regulatory overclaims, or incomplete explanations.
• Highly detail-oriented and organized, with the ability to maintain style guides, FAQs, trackers, onboarding materials, honeypots, calibration tasks, and other quality documentation.
Preferred:
• Familiarity with common biomedical engineering tools or workflows such as MATLAB, Python, LabVIEW, SolidWorks, CAD/CAE tools, signal processing workflows, medical device documentation, ISO/FDA-related documentation, clinical engineering workflows, or biomedical data analysis tools.
• Experience leading or supporting remote teams of trainers, annotators, reviewers, engineers, technical writers, or QAs.
• Comfortable working in fast-moving remote environments using tools such as Discord, Google Sheets, Google Docs, trackers, dashboards, and project management systems.
• Experience with AI training, data annotation, large language models, prompt/response evaluation, technical content QA, biomedical content QA, or rubric-based LLM evaluation.
Company:
Our Core mission is to develop, deploy, or integrate artificial intelligence (AI) — including machine learning (ML), data analytics, automation, natural language processing (NLP), computer vision, and related technologies — to solve real-world problems, improve decision-making, automate repetitive tasks, and deliver intelligent solutions across industries. Founded in 2018, the company is headquartered in Abu Dhabi, Abu Dhabi Emirate, AE, , with a team of 51-200 employees. The company is currently Growth Stage.
YO IT Consulting is a fast-growing AI Data Services company delivering training data for major AI companies. They are seeking a Biomedical Engineering Quality Assurance Lead to oversee quality and consistency across biomedical engineering AI training projects, review AI-generated content, and ensure adherence to quality standards.
Responsibilities:
• Quality monitoring: Spot-check biomedical engineering items, identify quality issues, provide ongoing feedback through DMs, and escalate recurring or critical issues.
• Technical review: Evaluate AI-generated biomedical engineering explanations, medical-device reasoning, biomechanics calculations, biomaterials discussions, bioinstrumentation workflows, biosignal explanations, diagrams/descriptions, and problem-solving steps for correctness and clarity.
• Trainer and QA communication: Update trainers and QAs on Discord about new item guidelines, project changes, workflow updates, quality expectations, and biomedical-engineering-specific review standards.
• Question handling: Respond to trainer/QA questions clearly and promptly, especially around engineering assumptions, units, formulas, biological context, device safety, regulatory considerations, standards references, and rubric interpretation.
• Trainer/QA activation management: DM contributors who are inactive or not working, encourage activation, track follow-ups, and flag availability issues when needed.
• Documentation: Create and maintain biomedical engineering project documentation, including style guides, trackers, FAQs, quality notes, examples, honeypots, calibration tasks, and onboarding materials.
• Onboarding and training: Schedule and run onboarding/training calls with trainers and QAs to explain project expectations, workflows, rubrics, quality standards, and biomedical-engineering-specific review requirements.
• Quality alignment: Ensure all trainers and QAs apply biomedical engineering guidelines consistently and understand updates as projects evolve.
• Risk and safety review: Flag unsafe, misleading, or overconfident biomedical engineering recommendations, especially where medical devices, patient safety, clinical workflows, biological systems, diagnostics, imaging, rehabilitation tools, or regulatory claims may be affected.
• Process improvement: Identify recurring quality gaps, propose workflow improvements, and help build scalable QA processes for biomedical engineering AI training projects.
Qualifications:
Required:
• Bachelor’s or Master’s degree in Biomedical Engineering, Bioengineering, Medical Engineering, Biomechanical Engineering, Electrical Engineering with biomedical focus, Mechanical Engineering with biomedical focus, or a closely related field.
• Strong grasp of the English language to follow project guidelines, communicate with teams, and provide clear technical feedback in English.
• 3+ years of professional experience in biomedical engineering, medical devices, biomechanics, biomaterials, bioinstrumentation, clinical engineering, R&D, regulatory documentation, technical review, engineering education, or related workflows.
• Strong understanding of core biomedical engineering topics such as biomechanics, biomaterials, medical devices, bioinstrumentation, biosignals, imaging systems, physiological systems, tissue engineering, rehabilitation engineering, and biomedical data analysis.
• Ability to evaluate biomedical engineering content against detailed rubrics and identify issues such as incorrect assumptions, flawed calculations, missing units, unsafe recommendations, weak biological/clinical reasoning, hallucinated standards, regulatory overclaims, or incomplete explanations.
• Highly detail-oriented and organized, with the ability to maintain style guides, FAQs, trackers, onboarding materials, honeypots, calibration tasks, and other quality documentation.
Preferred:
• Familiarity with common biomedical engineering tools or workflows such as MATLAB, Python, LabVIEW, SolidWorks, CAD/CAE tools, signal processing workflows, medical device documentation, ISO/FDA-related documentation, clinical engineering workflows, or biomedical data analysis tools.
• Experience leading or supporting remote teams of trainers, annotators, reviewers, engineers, technical writers, or QAs.
• Comfortable working in fast-moving remote environments using tools such as Discord, Google Sheets, Google Docs, trackers, dashboards, and project management systems.
• Experience with AI training, data annotation, large language models, prompt/response evaluation, technical content QA, biomedical content QA, or rubric-based LLM evaluation.
Company:
Our Core mission is to develop, deploy, or integrate artificial intelligence (AI) — including machine learning (ML), data analytics, automation, natural language processing (NLP), computer vision, and related technologies — to solve real-world problems, improve decision-making, automate repetitive tasks, and deliver intelligent solutions across industries. Founded in 2018, the company is headquartered in Abu Dhabi, Abu Dhabi Emirate, AE, , with a team of 51-200 employees. The company is currently Growth Stage.