310 Medical Engineering jobs in the United States
ASCP Certified Bio-Medical Engineering Technician
Posted 3 days ago
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Job Description
Join a dedicated healthcare team in the heart of the Midwest region, where your expertise as a Bio-Medical Engineering Technician will play a vital role in supporting clinical operations. This full-time day position involves independent work on repairing, safety testing, and preventive maintenance of a variety of clinical medical equipment.
General Summary
As a Bio-Medical Engineering Technician, you will be responsible for inspecting, installing, calibrating, and maintaining medical and technical equipment used by healthcare professionals for diagnosis, treatment, and research. Ensuring safety for patients and staff through rigorous testing of equipment and facility environments is a key part of this role.
Essential Duties and Responsibilities
- Perform repairs, calibrations, and maintenance on medical instrumentation and equipment.
- Conduct safety tests to prevent electrical or mechanical hazards within the healthcare setting.
- Maintain detailed records of all work performed using specialized bio-medical software systems.
- Manage ordering and coordination of replacement parts and external repair services.
- Communicate effectively with vendors and equipment users to ensure timely and proper maintenance outcomes.
- Lead or participate in training sessions to educate staff on equipment use and safety.
- Share knowledge and cross-train fellow bio-medical technicians to enhance team capabilities.
Education
A high school diploma or equivalent is required. An associate degree or equivalent experience, such as military training or technical school, is preferred.
Experience
Three to five years of experience in bio-medical equipment maintenance is preferred.
Certification/License
Certification as a Certified Biomedical Equipment Technician (CBET) is preferred.
Mental/Physical Requirements
This role requires standing, walking, sitting, reaching, squatting, kneeling, and the ability to lift up to 75 pounds. Good eyesight, steady hands, and the ability to perform under stress are essential.
Working Conditions
Technicians may come into contact with patients and encounter various environmental conditions including exposure to heat, cold, noise, chemicals, infectious diseases, and hazardous waste. Occasional overnight travel for training may be required.
Electrical Engineer (medical devices)
Posted today
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Job Description
We’re ALTEN Technology USA, an engineering services company helping clients bring groundbreaking ideas to life—from advancing space exploration and life-saving medical devices to building autonomous electric vehicles. With 3,000+ experts across North America, we partner with leading companies in aerospace, medical devices, robotics, automotive, commercial vehicles, EVs, rail, and more.
As part of the global ALTEN Group—57,000+ engineers in 30 countries—we deliver across the entire product development cycle, from consulting to full project outsourcing.
When you join ALTEN Technology USA, you’ll collaborate on some of the world’s toughest engineering challenges, supported by mentorship, career growth opportunities, and comprehensive benefits.
Responsibilities:
- Lead surface coil failure investigation and root cause analysis
- Collaborating with the service team to gather failure data from customer sites
- Working with MRI systems for data collection and coil performance evaluation
- Demonstrating strong analytical and communication skills throughout the process
- Applying electrical circuit board design and simulation expertise using tools such as Cadence, Altium, and ADS
Education and Experience:
- BS in Electrical Engineering or related discipline with 1 to 3 years of relevant experience
Qualifications:
- Knowledge of standard drafting practices, product structuring, electronics modeling and drawing practices, and engineering analysis techniques.
- Knowledge of Analog and RF circuit design
- Understanding of engineering product development processes
Desired Qualifications:
- Master’s degree in electrical engineering
- Medical device experience
- Demonstrated experience in the following: Electromagnetics, Transmission Line design, Antenna Theory & Design, Mixers, Oscillators, Amplifiers, Analog Design, RF Printed Circuit Board Layout experience
- Experience with Weibull Analysis and DFR (Design for Reliability) tools
- Self-starter, energizing, results oriented, and able to multi-task
Location: Hybrid (3 days), in Aurora OH
Salary Range: $65K-$96K
- The actual salary offered is dependent on various factors including, but not limited to, location, the candidate’s combination of job-related knowledge, qualifications, skills, education, training, and experience
Software Engineer - Medical Devices
Posted today
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Job Description
Aneuvo is a platform and therapy development company focused on treating chronic injuries and conditions that have not been curable through traditional pharmaceutical approaches. By joining our team, you will have the opportunity to create meaningful change for patients and families whose lives have been significantly impacted by chronic injuries and/or conditions.
We are currently looking for a Software Developer who wants to apply their expertise to develop new medical devices and technologies. This is a unique opportunity to work on a project that has a direct and immediate impact on improving human life. You will also be exposed to all phases of medical technology development as well as closely work with an energetic team filled with highly varied domain expertise. An ideal candidate enjoys taking challenges and often exceeds expectations.
Responsibilities
· Design, develop, and maintain embedded and/or application-level software for medical devices.
· Implement software solutions in compliance with IEC 62304, ISO 13485, and applicable FDA/CE
regulations.
· Collaborate with electrical, mechanical, and biomedical engineers to ensure seamless hardware/software
integration.
· Participate in design reviews, code reviews, and risk assessments.
· Develop and execute unit, integration, and system-level software tests.
· Create and maintain design documentation, traceability matrices, and verification reports.
· Support verification, validation, and regulatory submission activities.
· Troubleshoot and resolve software issues during development, testing, and post-market phases.
· Contribute to continuous improvement of the software development process.
Requirements to Apply:
- Master's or Bachelor's degree in Computer Science or equivalent
- 7+ years of professional software development experience, ideally in the medical device industry
- Proficiency in two or more programming languages: Java, Kotlin, Python, JavaScript
- Strong experience with Android application development
- Strong experience with service APIs and/or SDKs
- Several years of experience in Agile/SCRUM enterprise-scale software development
- Experience with OAuth or JWT authentication and front-end security best practices
- Experience with DevOps and code versioning tools (Git, Bitbucket, etc.)
- Deep understanding of cross-browser, cross-device, and web performance optimization
- Strong written and oral communication skills in English with ability to effectively collaborate with customers, management, and engineering teams
- Strong analytical and problem-solving skills
Preferred Qualifications:
- Experience with Class II or Class III medical device development
- Knowledge of wireless protocols (Bluetooth Low Energy, Wi-Fi)
- Knowledge of signal processing, control systems, or bioelectronic interfaces
- Familiarity with cybersecurity considerations for medical devices (FDA guidance, ISO/IEC 27001)
- Experience with automated testing frameworks
- Experience in web application development
Technical Writer - Medical Devices
Posted today
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Job Description
Our client, a leading medical devices manufacturing company, is looking for a Technical Writer – Medical Devices. This is for an initial duration of 12 months and is located in San Diego, CA.
Job Type: Contract (Candidates must be able to work on W2 without VISA sponsorship)
Job Summary:
- The Technical Writer will be responsible for developing, writing, and maintaining comprehensive technical documentation for our Class II medical devices.
- This role requires a detail-oriented professional with strong writing skills and a deep understanding of regulatory requirements.
- The ideal candidate will have extensive experience in the medical device industry and the ability to work effectively with cross-functional teams.
Qualifications:
- Experience working in a regulated industry such as medical devices or pharmaceuticals.
- Extensive experience with regulatory compliance processes. Strong background in supporting regulatory requirements to ensure adherence to regulatory guidelines.
- Demonstrated ability to be highly collaborative with marketing, clinical, quality, and regulatory reviewers.
- Five or more years writing and editing hardware/software user guides (print and online) and other technical product documentation.
- Ability to effectively manage the delivery of prioritized tasks.
- Ability to demonstrate a high level of initiative to gather information for developing documentation.
- Ability to work independently with minimal supervision.
- Effective at thinking independently and solving problems with product core team members.
- Ability to work under compressed deadlines and must be able to deal with unresolved situations, frequent project changes, delays, or other events.
- Ability to handle multiple projects with excellent follow-up and project management skills.
- Familiarity with electro-mechanical concepts and software application usage.
- Experience in device labeling and/or packaging content development.
- Familiarity with large company engineering change control processes and Agile software development methodologies.
- Experience with SAP, Oracle, or similar enterprise resource planning (ERP) system is a plus.
- Experience in version control systems (VCS) such as, Perforce, Apache Subversion, Microsoft Team Foundation Server, or GitHub.
- Knowledge of photography and photo editing software such as Adobe Photoshop.
- Skilled in both electronic and hard copy markup (Acrobat, tracked changes in Microsoft Word, standard editorial and proofreading symbols).
- Knowledge and experience with desktop publishing (DTP) software applications (MadCap Flare, Adobe FrameMaker, Adobe InDesign, Adobe Illustrator, XML, DITA) as applicable for technical documentation.
Compensation: The hourly rate for this position is between $47-$50 per hour.
Factors which may affect starting pay within this range may include (geography/market, skills, education, experience and other qualifications of the successful candidate).
Software Engineer - Medical Devices
Posted 3 days ago
Job Viewed
Job Description
Aneuvo is a platform and therapy development company focused on treating chronic injuries and conditions that have not been curable through traditional pharmaceutical approaches. By joining our team, you will have the opportunity to create meaningful change for patients and families whose lives have been significantly impacted by chronic injuries and/or conditions.
We are currently looking for a Software Developer who wants to apply their expertise to develop new medical devices and technologies. This is a unique opportunity to work on a project that has a direct and immediate impact on improving human life. You will also be exposed to all phases of medical technology development as well as closely work with an energetic team filled with highly varied domain expertise. An ideal candidate enjoys taking challenges and often exceeds expectations.
Responsibilities
Design, develop, and maintain embedded and/or application-level software for medical devices.
Implement software solutions in compliance with IEC 62304, ISO 13485, and applicable FDA/CE
regulations.
Collaborate with electrical, mechanical, and biomedical engineers to ensure seamless hardware/software
integration.
Participate in design reviews, code reviews, and risk assessments.
Develop and execute unit, integration, and system-level software tests.
Create and maintain design documentation, traceability matrices, and verification reports.
Support verification, validation, and regulatory submission activities.
Troubleshoot and resolve software issues during development, testing, and post-market phases.
Contribute to continuous improvement of the software development process.
Requirements to Apply:
- Master's or Bachelor's degree in Computer Science or equivalent
- 7+ years of professional software development experience, ideally in the medical device industry
- Proficiency in two or more programming languages: Java, Kotlin, Python, JavaScript
- Strong experience with Android application development
- Strong experience with service APIs and/or SDKs
- Several years of experience in Agile/SCRUM enterprise-scale software development
- Experience with OAuth or JWT authentication and front-end security best practices
- Experience with DevOps and code versioning tools (Git, Bitbucket, etc.)
- Deep understanding of cross-browser, cross-device, and web performance optimization
- Strong written and oral communication skills in English with ability to effectively collaborate with customers, management, and engineering teams
- Strong analytical and problem-solving skills
Preferred Qualifications:
- Experience with Class II or Class III medical device development
- Knowledge of wireless protocols (Bluetooth Low Energy, Wi-Fi)
- Knowledge of signal processing, control systems, or bioelectronic interfaces
- Familiarity with cybersecurity considerations for medical devices (FDA guidance, ISO/IEC 27001)
- Experience with automated testing frameworks
- Experience in web application development
Project Manager, Medical Devices
Posted 1 day ago
Job Viewed
Job Description
**Working at Abbott**
At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to:
+ Career development with an international company where you can grow the career you dream of.
+ Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
+ An excellent retirement savings plan with a high employer contribution
+ Tuition reimbursement, the Freedom 2 Save ( student debt program, and FreeU ( education benefit - an affordable and convenient path to getting a bachelor's degree.
+ A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
+ A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.
**The Opportunity**
This position works out of our Pleasanton, CA location in the Heart Failure Division. In Abbott's Heart Failure (HF) business, we're developing solutions to diagnose, monitor and manage heart failure, allowing people to restore their health and get on with their lives.
Project Manager for the Supplier Excellence Taskforce aims is to achieve material stabilization through design optimization, improved inspection and process controls, in conjunction with supplier management and component qualifications. You will manage project timelines, budgets, and deliverables, ensuring compliance with regulatory requirements.
**What You'll Work On**
+ **Lead cross-functional project teams** to drive supplier quality initiatives, ensuring alignment with medical device regulatory standards (e.g., FDA, ISO 13485).
+ **Develop and manage detailed project plans** , timelines, budgets, and deliverables with a focus on supplier performance and risk mitigation.
+ **Monitor supplier quality metrics** and project progress, proactively identifying issues and implementing corrective actions to maintain compliance and minimize delays.
+ **Coordinate supplier visits, validations, and qualifications** , ensuring documentation and processes meet internal and external regulatory requirements.
+ **Collaborate with engineering, quality, and procurement teams** to define technical requirements and ensure suppliers meet product specifications and quality expectations.
+ **Prepare and present project status reports** to stakeholders, highlighting risks, milestones, and quality-related outcomes.
+ **Manage external contractors and suppliers** , ensuring integration into project workflows and adherence to quality standards.
+ **Drive continuous improvement initiatives** across supplier quality processes, leveraging data and feedback to enhance operational efficiency.
+ **Ensure project documentation** (e.g., design history files, CAPAs, change controls) is complete, accurate, and audit-ready.
+ **Facilitate cross-functional meetings** , set priorities, allocate tasks, and guide project staff to meet key deliverables and regulatory milestones.
**Required Qualifications**
+ Bachelor's degree in related field or an equivalent combination of education and work experience
+ 4+ years of relevant experience
**Preferred Qualifications**
+ Experience in the medical devices or similar field
+ A self-directed, efficient individual with excellent analytical and problem-solving skills.
+ Must have excellent project and time management skills with the ability to manage multiple projects and tasks.
Apply Now ( more about our health and wellness benefits, which provide the security to help you and your family live full lives:** ( your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at , on Facebook at , and on Twitter @AbbottNews.
The base pay for this position is $86,700.00 - $173,300.00. In specific locations, the pay range may vary from the range posted.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
Sales Representative Medical Devices
Posted 1 day ago
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Job Description
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Radiometer, one of Danaher's ( 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.
You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.
At Radiometer, life comes first. Our vision is to improve global healthcare with reliable, fast, and easy patient diagnoses. As a global leader and pioneer in acute care diagnostics for over 70 years, we streamline diagnostic workflows, empowering healthcare professionals to focus on what truly matters-caring for critically ill patients. Here, you'll find a place to grow and make a real impact with your unique perspective, driving us forward in improving patient care.
Learn about the Danaher Business System ( which makes everything possible.
The Radiometer Sales Representative is tasked with building and nurturing customer relationships, proactively identifying new business opportunities, and enhancing sales growth with existing clients. The Sales Representative is responsible for creating and executing a territory plan to deliver year over year installed base and core growth directed by annual performance objectives and quota.
This position reports to the Regional Sales Manager and is part of the Blood Gas Sales Team and will be remote , responsible for a territory in and around Minneapolis, Minnesota including the Dakotas. The position requires a minimum of 70% travel throughout the territory including overnight travel.
In this role, you will have the opportunity to:
+ Create and execute a territory plan, ensuring we win new customers, retain our base business, and expand our footprint in existing accounts to expand revenue growth.
+ Progress sales funnel and sales advances with onsite sales calls.
+ Conduct annual customer business reviews of top accounts and assist in managing escalated accounts in coordination with regional support team.
+ Maintain accurate sales funnel, customer contacts, activities and forecast in Customer Relationship Management (CRM) system.
+ Deliver highest value proposals to meet customers' needs while meeting company growth objectives.
The essential requirements of the job include:
+ Bachelor's degree required, science major preferred
+ 3+ years sales experience required; in a medical device industry preferred
+ 1+ years capital equipment sales experience preferred
Travel, Motor Vehicle Record & Physical/Environment Requirements:
+ Up to 70% travel or greater; some overnight travel
+ Must have a valid driver's license and a clean driving record for the last 3 years
+ Ability to lift, move or carry equipment up to 50 pounds
It would be a plus if you also possess previous experience in:
+ Respiratory therapy, nurse, clinical lab or similar work experience helpful.
+ An understanding of business management systems, including Microsoft Office (Word, Excel, Outlook), database and CRM
Radiometer, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info ( .
At Radiometer, we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Radiometer can provide.
The salary range for this role is $90,000 - $100,000 . This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.
This job is also eligible for bonus/incentive pay.
We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.
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Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit .
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.
The U.S. EEO posters are available here ( .
We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact: or .
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Project Manager - Medical Devices
Posted today
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Job Description
The Project Manager will lead key strategic new product development initiatives from concept through commercialization, ensuring seamless cross-functional coordination between key internal departments. This position will require strong project management experience in design and development projects within an FDA regulated industry, as well as strong knowledge of design control processes and supply chain concepts. This role will establish and maintain project management infrastructure that drives accountability, transparency, and on-time delivery across the company's portfolio of new product development projects.
Responsibilities:
- Manage the complete lifecycle of major new product development projects from concept through market launch
- Create detailed project plans including scope, timelines, and resource allocation
- Lead project meetings and coordinate with stakeholders across marketing, operations, R&D, regulatory, and sales
- Track project performance and provide regular updates to senior leadership and stakeholders
- Maintain project portfolio visibility through dashboards and reporting mechanisms
- Identify and mitigate project risks while managing plan deviations and conducting impact analysis
- Develop standardized PM templates, governance structures, and best practices tailored to marketing needs
- Establish a scalable PMO with lightweight tools and processes that product managers can utilize for smaller initiatives
- Coordinate resource planning and change management across functional teams
Requirements:
- Bachelor’s Degree required (Engineering, Science, Management or related discipline), Masters/MBA degree preferred
- At least 5 years’ working experience with 2+ years’ experience in Project Management
- Medical device or regulated industry experience strongly preferred
- PMP certification or equivalent preferred
- Proficient knowledge of Project Management methodologies, tools, and best-known practice
- Proven ability to manage product development or marketing projects
Skills:
- Experience with SmartSheet preferred; proficiency in project management software required
- Strong knowledge of project management methodologies and best practices
- Exceptional organizational, analytical, and problem-solving skills
- Outstanding verbal and written communication abilities
- Influential leadership style with strong matrix management capabilities
- Strategic thinking with ability to articulate vision and secure stakeholder buy-in
- Ability to manage multiple complex initiatives simultaneously
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Electrical Engineer (medical devices)
Posted today
Job Viewed
Job Description
We’re ALTEN Technology USA, an engineering services company helping clients bring groundbreaking ideas to life—from advancing space exploration and life-saving medical devices to building autonomous electric vehicles. With 3,000+ experts across North America, we partner with leading companies in aerospace, medical devices, robotics, automotive, commercial vehicles, EVs, rail, and more.
As part of the global ALTEN Group—57,000+ engineers in 30 countries—we deliver across the entire product development cycle, from consulting to full project outsourcing.
When you join ALTEN Technology USA, you’ll collaborate on some of the world’s toughest engineering challenges, supported by mentorship, career growth opportunities, and comprehensive benefits.
Responsibilities:
- Lead surface coil failure investigation and root cause analysis
- Collaborating with the service team to gather failure data from customer sites
- Working with MRI systems for data collection and coil performance evaluation
- Demonstrating strong analytical and communication skills throughout the process
- Applying electrical circuit board design and simulation expertise using tools such as Cadence, Altium, and ADS
Education and Experience:
- BS in Electrical Engineering or related discipline with 1 to 3 years of relevant experience
Qualifications:
- Knowledge of standard drafting practices, product structuring, electronics modeling and drawing practices, and engineering analysis techniques.
- Knowledge of Analog and RF circuit design
- Understanding of engineering product development processes
Desired Qualifications:
- Master’s degree in electrical engineering
- Medical device experience
- Demonstrated experience in the following: Electromagnetics, Transmission Line design, Antenna Theory & Design, Mixers, Oscillators, Amplifiers, Analog Design, RF Printed Circuit Board Layout experience
- Experience with Weibull Analysis and DFR (Design for Reliability) tools
- Self-starter, energizing, results oriented, and able to multi-task
Location: Hybrid (3 days), in Aurora OH
Salary Range: $65K-$96K
- The actual salary offered is dependent on various factors including, but not limited to, location, the candidate’s combination of job-related knowledge, qualifications, skills, education, training, and experience
Equipment Manager/Medical Devices
Posted today
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Job Description
Sean Ianchulev, is dedicated to meaningful innovation in glaucoma care. The company develops next-generation bio & micro-interventional technologies for complete natural outflow enhancement, advancing treatment options for patients worldwide. With a mission to transform eye care, Iantrek combines clinical expertise and pioneering design to deliver impactful solutions to elevate the standard of glaucoma management.
Role Overview We are seeking dynamic, driven Surgical Glaucoma Manager to join our growing commercial team. In-depth understanding of market access.
· Build physician advocacy within ASCs and Academic training programs. Represent Iantrek at key congresses, wet labs, and local events.
· Partner with cross-functional teams (clinical, marketing, training) to support surgeon onboarding and utilization.
· Maintain accurate and timely records in the company CRM, ensuring pipeline visibility and accountability.
· Qualifications · 5+ years of experience in ophthalmic sales, medical devices (Surgical Glaucoma preferred).
· Self-starter with excellent communication, organizational, and relationship-building skills.
· Willingness to travel within assigned territory and occasionally nationwide.
Be part of a commercial launch moment that will shape the future of glaucoma care.
· Competitive compensation, benefits, and long-term career growth opportunities.