Summary The Sr Design Engineer is responsible for Design medical devices to support the growth ... 62304 (Medical Device Software Lifecycle Requirements) preferred. * Strong familiarity with the ...
Summary The Sr Design Engineer is responsible for Design medical devices to support the growth ... 62304 (Medical Device Software Lifecycle Requirements) preferred. * Strong familiarity with the ...
Software Engineer, On Device
Ann Arbor, MI · On-site +1
$120K - $150K/yr
We are expanding our engineering team and looking for a Software Engineer to support the ... medical condition, pregnancy or childbirth, sexual orientation, genetics, genetic information ...
Software Engineer, On Device
Ann Arbor, MI · On-site +1
$120K - $150K/yr
We are expanding our engineering team and looking for a Software Engineer to support the ... medical condition, pregnancy or childbirth, sexual orientation, genetics, genetic information ...
Sr Design Engineer
Caledonia, MI · On-site
Summary The Sr Design Engineer is responsible for Design medical devices to support the growth ... 62304 (Medical Device Software Lifecycle Requirements) preferred. * Strong familiarity with the ...
Sr Design Engineer
Caledonia, MI · On-site
Summary The Sr Design Engineer is responsible for Design medical devices to support the growth ... 62304 (Medical Device Software Lifecycle Requirements) preferred. * Strong familiarity with the ...
Integration Engineer (Embedded or Test Engineer)-Automotive/Medical device exprience
Ann Arbor, MI · On-site
$101K - $137K/yr
Integration Engineer (Embedded or Test Engineer)-Automotive/Medical device exprience * We are ... Automotive and/or embedded software experience will be valued, or alternatively experience building ...
Quick apply
Integration Engineer (Embedded or Test Engineer)-Automotive/Medical device exprience
Ann Arbor, MI · On-site
$101K - $137K/yr
Integration Engineer (Embedded or Test Engineer)-Automotive/Medical device exprience * We are ... Automotive and/or embedded software experience will be valued, or alternatively experience building ...
Software Engineer
Dearborn, MI · On-site
Overview We are looking for a skilled Software Engineer to design and deliver scalable, cloud ... device and data integrations. Responsibilities * Design and develop RESTful and event-driven ...
Quick apply
Software Engineer
Dearborn, MI · On-site
Overview We are looking for a skilled Software Engineer to design and deliver scalable, cloud ... device and data integrations. Responsibilities * Design and develop RESTful and event-driven ...
Software Engineer
Dearborn, MI · On-site
Overview We are looking for a skilled Software Engineer to design and deliver scalable, cloud ... device and data integrations. Responsibilities * Design and develop RESTful and event-driven ...
Software Engineer
Dearborn, MI · On-site
Overview We are looking for a skilled Software Engineer to design and deliver scalable, cloud ... device and data integrations. Responsibilities * Design and develop RESTful and event-driven ...
Overview We are looking for a skilled Software Engineer to design and deliver scalable, cloud ... device and data integrations. Responsibilities * Design and develop RESTful and event-driven ...
Overview We are looking for a skilled Software Engineer to design and deliver scalable, cloud ... device and data integrations. Responsibilities * Design and develop RESTful and event-driven ...
Software Engineer
Dearborn, MI · On-site
Software Engineer ON W2 Location: On-site in Dearborn, MI, 5 days a week JD: Java • Spring Boot ... device and data integrations. Responsibilities • Design and develop RESTful and event-driven ...
Software Engineer
Dearborn, MI · On-site
Software Engineer ON W2 Location: On-site in Dearborn, MI, 5 days a week JD: Java • Spring Boot ... device and data integrations. Responsibilities • Design and develop RESTful and event-driven ...
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Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...
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Flint, MI · On-site
Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...
Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...
Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...
Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...
Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...
Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...
Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...
Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...
Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...
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Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...
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Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...
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Kalamazoo, MI · On-site
Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...
Medical Device Software Engineer information
See Michigan salary details
$55.3K - $66.6K
2% of jobs
$66.6K - $77.8K
4% of jobs
$77.8K - $89.1K
6% of jobs
$89.1K - $100.4K
8% of jobs
$106.4K is the 25th percentile. Wages below this are outliers.
$100.4K - $111.6K
7% of jobs
$111.6K - $122.9K
18% of jobs
The median wage is $125.5K / yr.
$122.9K - $134.1K
16% of jobs
$134.1K - $145.4K
2% of jobs
$150K is the 75th percentile. Wages above this are outliers.
$145.4K - $156.6K
26% of jobs
$156.6K - $167.9K
1% of jobs
$167.9K - $179.1K
8% of jobs
$55.3K
$128.6K
$179.1K
How much do medical device software engineer jobs pay per year?
What are the key skills and qualifications needed to thrive in the Medical Device Software Engineer position, and why are they important?
To thrive as a Medical Device Software Engineer, you need a solid background in software development, embedded systems, and biomedical engineering, often supported by a degree in computer science, electrical engineering, or a related field. Experience with programming languages like C/C++, knowledge of real-time operating systems, and familiarity with medical device regulatory standards such as IEC 62304 are typically required. Strong problem-solving skills, attention to detail, and effective communication are essential soft skills for this position. These skills ensure high-quality, compliant software that contributes to safe and reliable medical devices, which are critical for patient health.
What is a Medical Device Software Engineer job?
A Medical Device Software Engineer is responsible for designing, developing, testing, and maintaining software used in medical devices. They ensure compliance with regulatory standards like FDA and IEC 62304 while working on embedded systems, user interfaces, or cloud-based healthcare applications. Their role involves collaborating with cross-functional teams, including hardware engineers and regulatory specialists, to ensure patient safety and product effectiveness.
What are some typical daily responsibilities of a Medical Device Software Engineer?
Medical Device Software Engineers typically spend their days designing, coding, and testing software for medical devices in compliance with health regulations. They collaborate closely with hardware engineers, quality assurance teams, and regulatory specialists to ensure that the software integrates seamlessly with device hardware and meets performance and safety standards. Documenting development processes, participating in code reviews, and addressing feedback from cross-functional teams are also common aspects of the role. This position often requires troubleshooting issues in both simulated and real clinical environments to ensure the reliability and safety of the device.
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Other
Posted 27 days ago
Job description
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Summary
The Sr Design Engineer is responsible for Design medical devices to support the growth, cost profile, and business continuity of Aspen Surgical products while working in a collaborative team environment.
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In This Position, You Will Have the Opportunity to:
- Support design tasks associated with global revenue growth and margin improvement projects
- Support organic growth functions of acquisitions and other business migrations
- Support sustaining engineering functions of the organization to maintain business continuity
Medical Device Product Development
- Execute medical device design history file activities to be compliant with applicable regulations
- Conduct the development and evaluation of medical device designs which meet defined product requirements and that are optimized for safe clinical solutions, production, reliability, and overall cost effectiveness for the business
- Provide technical assistance to various departments and individuals as necessary in the exploration of new opportunities
- Evaluate proposed changes to existing products and complete deliverables required to implement the change through individual efforts or cross-functional teams
- Ensure that product changes meet regulations as well as internal and external customer requirements
- Troubleshoot and problem-solve efforts related to product design.
- Conduct thorough engineering and data analysis.
Project Management
- Responsible for project schedules, budgets, mitigating risks, and efficient solutioning of issues
- Recommend and communicate project plans, track tasks, and manage time to meet project deadlines
- Executive presence for communicating with leaders in a clear efficient manner
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Global Collaboration
- Work closely with the portfolio managers to understand clinical and commercial impacts.
- Strong communication skills to convey design concepts to clinicians to obtain design direction
- Work with manufacturing throughout the development phases to ensure that products are produced in a safe, efficacious, and quality manner while keeping within established time frames
- Work with finance to develop product costing to understand impacts of material/design selections
- Interface with vendors, manufacturing facilities, and various internal groups to resolve design and manufacturing issues of new and existing products
- Provide peer mentoring and guidance to other engineers throughout the company
What You Need to Succeed in This Position
- Bachelor of Science Degree in Engineering or closely related 4-year technical degree is required
- 7+ years of medical device engineering experience preferred
- PMP certification preferred
- Regulated industry experience that includes, but not limited to, FDA 21CFR820.30, ISO 13485, ISO 14971, MDSAP and European MDD/MDR requirements.
- Working knowledge with ISO 11607 regulations and transit testing to ASTM 4169 or similar testing standards
- Experience with IEC 60601 (Medical Electrical Equipment Safety and Performance Requirements) and/or IEC 62304 (Medical Device Software Lifecycle Requirements) preferred.
- Strong familiarity with the methods of Risk Management and Failure Mode Effects Analysis (FMEA)
- Working knowledge of design history & technical file within an auditing environment.
- Working knowledge of statistical analysis of data used to meet or define design criteria
- Project management experience to effectively manage and complete multiple projects simultaneously
- Involvement with invention disclosures or patents
- Business case development for product costing as it pertains to design
- Preferred experience using engineering programs such as SolidWorks, Minitab, TOPS, similar.
- Teamwork, effective communication, and positive attitude required to fit & grow culture
- Effectively handles global interactions and collaborations while managing cultural differences.
- Models clinical safety and quality first mindset
- Takes initiative and proactively mitigates risks
- Continuous education focused to advance job knowledge in medical device design & development
- Excellent computer skills including but not limited to Microsoft Office Suite
- On site job located in Caledonia, MI with 15% expected travel