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Mechanical Engineer Medical Device Jobs (NOW HIRING)

Senior Mechanical Engineer - Medical Devices Are you passionate about bringing medical technologies ... medical device solutions. * Plan and execute prototype builds, testing activities, and design ...

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Lead system integration across electrical, mechanical, optical, firmware, and software subsystems ... and Class II medical device design controls. * Help stand up engineering processes and ...

Mechanical Engineer - Sustaining Engineering Location: Madison East (Onsite) Employment Type ... Medical device or regulated industry experience strongly preferred Skills: MECHANICAL,CAD

Mechanical Engineer

Bedford, MA · On-site

$85K - $100K/yr

Lexington Medical, Inc. is a medical device company developing and manufacturing minimally invasive ... We are hiring a Mechanical Engineer to join Lexington Medical's R&D team in Bedford, MA. Ideal for ...

Lexington Medical, Inc. is a medical device company developing and manufacturing minimally invasive ... We are hiring a Mechanical Engineer to join Lexington Medical's R&D team in Bedford, MA. Ideal for ...

Lexington Medical, Inc. is a medical device company developing and manufacturing minimally invasive ... We are hiring a Mechanical Engineer to join Lexington Medical's R&D team in Bedford, MA. Ideal for ...

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Mechanical Engineer Medical Device information

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$45.5K

$102.9K

$166.5K

How much do mechanical engineer medical device jobs pay per year?

As of Aug 12, 2026, the average yearly pay for mechanical engineer medical device in the United States is $102,878.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,500.00 and $126,500.00 per year, depending on experience, location, and employer.

Can mechanical engineers work on medical devices?

Yes, mechanical engineers can work on medical devices, designing and developing equipment such as surgical tools, imaging systems, and prosthetics. They often use CAD software, materials science knowledge, and regulatory standards to ensure device safety and functionality.

What are the typical daily responsibilities of a mechanical engineer medical device?

Mechanical Engineers in the medical device industry often spend their days designing, prototyping, and testing components or full systems using CAD and analysis tools. They actively collaborate with cross-functional teams, including biomedical engineers, quality assurance, and manufacturing, to refine designs and ensure regulatory compliance. Managing documentation, participating in design reviews, and supporting the transfer of products from development to production are also key aspects of the job. This role provides a dynamic mix of desk work, lab-based testing, and team interaction, offering a varied and rewarding work environment.

What are the key skills and qualifications needed to thrive as a mechanical engineer medical device?

Success as a Mechanical Engineer in the medical device field requires a solid background in mechanical engineering principles, CAD software proficiency, and an understanding of medical device regulations, typically supported by a relevant engineering degree. Hands-on experience with tools like SolidWorks, ANSYS, and knowledge of ISO 13485 or FDA regulations is often expected. Strong problem-solving, teamwork, and effective communication skills set top performers apart in this role. These competencies are vital for ensuring the design and manufacture of safe, reliable medical devices that meet strict industry standards.

What is a mechanical engineer medical device?

A Mechanical Engineer in the medical device industry designs, develops, and tests medical equipment and components. They ensure devices meet regulatory standards, improve functionality, and collaborate with cross-functional teams, including electrical engineers and healthcare professionals. Their work involves prototyping, material selection, and manufacturing processes to create safe and effective medical solutions.

More about Mechanical Engineer Medical Device jobs
What cities are hiring for Mechanical Engineer Medical Device jobs? Cities with the most Mechanical Engineer Medical Device job openings:
What are the most commonly searched types of Mechanical Engineer Medical Device jobs? The most popular types of Mechanical Engineer Medical Device jobs are:
What states have the most Mechanical Engineer Medical Device jobs? States with the most job openings for Mechanical Engineer Medical Device jobs include:
Infographic showing various Mechanical Engineer Medical Device 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 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $102,878 per year, or $49.5 per hour.

Development Engineer - Medical Device

Nuwellis, Inc

Eden Prairie, MN • On-site

$105K - $125K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 13 days ago


Job description

Nuwellis is not accepting resumes from 3rd party recruiters.
Development Engineer
Overview
If you're the kind of engineer who enjoys solving complex technical problems, likes taking ownership of your work, and wants to see your designs make a real difference for patients, we'd love to meet you.
As a Development Engineer, you'll play a key role in designing, developing, testing, and improving our innovative medical technology. Working alongside Engineering, Quality, Regulatory, Clinical, Marketing, and Operations, you'll contribute throughout the product lifecycle-from early design concepts through verification, validation, design transfer, and ongoing product improvements.
Because we're a smaller organization, you'll have the opportunity to be involved in far more than just one piece of the process. You'll work closely with experienced colleagues across multiple disciplines, have visibility into how decisions are made, and see the direct impact your work has on both our products and the patients who depend on them.
What You'll Do
  • Design, prototype, and evaluate electro-mechanical medical devices and disposable products.
  • Contribute throughout the product development lifecycle, from concept through commercialization and ongoing product improvements.
  • Develop engineering documentation, specifications, test protocols, reports, and Design History File documentation.
  • Plan and execute product verification and validation testing.
  • Participate in design reviews, risk assessments, and engineering change activities.
  • Support development efforts involving usability, biocompatibility, packaging, sterilization, shelf life, labeling, and test method validation.
  • Analyze engineering and test data to identify opportunities for product improvements and resolve technical challenges.
  • Partner with Quality, Regulatory, Clinical, Marketing, Operations, and external suppliers to move projects forward.
  • Support design transfer activities and product qualification while ensuring compliance with FDA Design Controls and applicable international standards.
  • Assist with root cause investigations and implementation of corrective actions.
  • Contribute to continuous improvement initiatives across products and engineering processes.

Requirements
What You'll Bring
• Bachelor's degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering, or a related engineering discipline.
• 3-6 years of experience developing medical devices.
• Experience working within FDA Design Controls and ISO 13485.
• Experience developing electro-mechanical products.
• Strong analytical and problem-solving skills.
• Excellent written and verbal communication skills.
• The ability to manage multiple priorities while working collaboratively across cross-functional teams.
It Would Be Great If You Also Have
• Experience with ISO 14971 risk management.
• Experience planning or executing verification and validation testing.
• Experience supporting design transfer into manufacturing.
• Experience working with contract manufacturers or suppliers.
• Familiarity with medical device standards such as IEC 60601, IEC 62366, ISO 10993, or similar.
Why Join Nuwellis?
At Nuwellis, you'll be part of a collaborative team where your ideas matter and your contributions are visible. Rather than being responsible for one small piece of a large organization, you'll have the opportunity to work across multiple phases of product development, collaborate directly with decision-makers, and help shape products that improve patient care.
What We Offer
We believe great people deserve great benefits. Here's a snapshot of what we offer:
• Salary: $105,000-$125,000 depending on experience and qualifications.
• Eligible for annual discretionary bonus.
• Medical insurance with multiple plan options, including a High Deductible Health Plan (HDHP) with an annual company HSA contribution of $2,000 for individual coverage or $4,000 for family coverage.
• Company contributions toward dental and vision insurance.
• Employer-paid life insurance (up to one times annual salary), plus short-term and long-term disability coverage.
• Generous Paid Time Off (PTO), floating holidays, and 8 paid company holidays.
• 401(k) plan with a 3% company match.
A Few Things You Should Know About Us
• You'll work closely with leaders across Medical Affairs, Clinical, Regulatory, Quality, Marketing, and Commercial.
• Your work will be visible and will have a meaningful impact on the organization.
• We value people who take initiative, ask thoughtful questions, and enjoy solving problems.
• We believe the best ideas can come from anyone, regardless of title.
• We appreciate people who are collaborative, dependable, adaptable, and willing to jump in wherever they're needed.
Any offer of employment is contingent upon the successful completion of a background check and drug screening.
Nuwellis participates in E-Verify. For more information, please visit http://www.uscis.gov/e-verify.
Salary Description
$105,000-$125,000