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Mechanical Engineer Medical Device Jobs (NOW HIRING)

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 hiring a Mechanical Engineer in Bedford, MA to design medical device mechanisms for our AEON surgical stapling platform. As a Mechanical Engineer at Lexington Medical, you ...

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 hiring a Mechanical Engineer in Bedford, MA to design medical device mechanisms for our AEON™ surgical stapling platform. As a Mechanical Engineer at Lexington Medical ...

Senior Systems Engineer (Medical Device)

Plymouth, MN · On-site

$109K - $149K/yr

Senior Systems Engineer (Medical Device) Duration: 12 Months Location: Plymouth, MN Only W2 ... A track record in electro-mechanical system development, preferably in medical devices or other ...

Showing results 41-60

Mechanical Engineer Medical Device information

See salary details

$45.5K

$102.9K

$166.5K

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

As of Sep 10, 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.

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.

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.

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 and must adhere to regulatory standards like FDA requirements to ensure safety and effectiveness.
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Infographic showing various Mechanical Engineer Medical Device job openings in the United States as of September 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $102,878 per year, or $49.5 per hour.

X-Ray Engineer (Medical Device)

Scottsdale, AZ • On-site

Other

Medical, Dental, Vision, Retirement, PTO

Re-posted 4 days ago


Job description

X-Ray Engineer

Ziehm Imaging - Orthoscan Inc. is currently seeking a motivated, career-oriented professional with a positive can-do attitude to join our team as a full-time X-Ray Engineer located in Scottsdale, AZ.

Why Work for Ziehm Imaging - Orthoscan Inc.? There's something special about Ziehm-Orthoscan. There's a sense of pride that comes from building a product that helps improve people's lives and making the most of ourselves as a company and as individuals. We know the success of Ziehm-Orthoscan depends on every employee in our organization; it is our people who make the difference.

What do we offer?

  • The challenge of meaningful work - we offer constant opportunities to grow and develop world-class skills and a truly rewarding career.
  • A unique culture where people convert their passion into action.
  • The kind of competitive compensation you would expect from a world leader.
  • Nine paid holidays plus a generous PTO and vacation time plan.
  • Great benefit plans, major medical, dental and vision.
  • Company 401(k) plan with an employer match.
  • Competitive salary commensurate with experience
Job Summary

Lead all engineering and production aspects of X-Ray Generation, including electrical high voltage design, glassware, heat management, and lean and quality production processes. Working closely with R&D, QARA, and Production, the X-Ray Engineer serves as the critical technical bridge between engineering design and manufacturing operations, architecting, designing, and developing next-generation X-ray generator assemblies, high-voltage subsystems, high-voltage insulation systems, and oil-filled assemblies from initial engineering concepts through final mass production. Leveraging a strong background in high-voltage testing methodologies and robust manufacturing processes, this role translates research and development concepts into scalable, manufacturable, high-power hardware by applying advanced root-cause analysis and problem-solving techniques. The position also utilizes excellent written and verbal communication skills to develop automated test procedures, manufacturing process documentation, work instructions, validation protocols, and factory acceptance criteria that ensure product quality, clinical reliability, manufacturing efficiency, and strict regulatory compliance.

Essential Functions
  • Own the electrical engineering design, conceptualization, and manufacturing transfer of X-ray generator assemblies, High-Voltage subsystems, High-Voltage insulation systems, and oil-filled assemblies, ensuring sound manufacturing methodologies are engineered directly into the initial layout. Develop technical solutions to achieve marketing/sales requirements to ISO13485 standards
  • Develop, maintain, and improve manufacturing processes, fixtures, work instructions, and acceptance criteria while designing and refining the underlying product architectures
  • Drive reliability improvements for X-ray generator assemblies, High-Voltage subsystems, insulation systems, and oil-filled assemblies by developing, implementing, and executing advanced, physical High-Voltage testing methodologies and validation protocols, ensuring all products are built, tested, and validated to IEC60601-1 4th edition standards
  • Lead data-driven failure analysis, root-cause investigations, corrective actions, and field-return evaluations to implement Engineering Change Orders (ECOs) that directly improve product performance and production yield.
  • Troubleshoot manufacturing, assembly, test, and performance issues related to High-Voltage and X-ray systems, verbally collaborating across R&D, QARA, and Production to deploy rapid, permanent technical solutions.
  • Identify and implement continuous improvement opportunities across processes, work instructions, product quality, and manufacturing efficiency to maintain statistical control of the production line.
  • Own the entire generator technical lifecycle—from incoming parts and assembly processes through burn-in, clinical reliability, and field-return investigations.
Basic Qualifications

Education:

  • Bachelor's degree in Electrical Engineering (BSEE) or a closely related engineering discipline with a strong academic focus in Power Electronics, Electromagnetic Field Theory, or High-Voltage Physics. An advanced Master's degree in Manufacturing Engineering or related disciplines is a plus.
  • 3+ years of progressive electrical or hardware engineering experience designing, developing, validating, and implementing complex high-power or high-voltage (kV-level) electrical systems, with demonstrated expertise in product development and production readiness.
  • 2+ years of progressive electrical engineering experience with demonstrated manufacturing engineering expertise, including manufacturing process development and new product introduction (NPI), is required, preferably in a medical device industry environment.

Experience:

  • High-Voltage testing & process transition experience in engineering or production test engineering (preferably in the medical/industrial X-ray industry), with a proven track record of implementing sound manufacturing processes and safely configuring high-power test benches operating between 40kV and 150kV
  • Structured failure investigation experience leading structured root-cause analysis and problem-solving techniques to dissect generator breakdowns, electrical arcs, and contamination events from factory burn-in failures through clinical field returns.
  • Cross-Functional technical communication: Demonstrated history of utilizing excellent written and verbal communication skills to bridge the gap between R&D, QARA, and Production—specifically transforming complex engineering requirements into audit-ready documentation and manufacturing work instructions.
Competencies
  • Mastery of specialized high-voltage test equipment, including digital oscilloscopes, high-voltage probes, insulation resistance testers, power analyzers, and partial discharge measurement systems
  • Comprehensive knowledge of high-voltage insulation systems, creepage and clearance design, dielectric breakdown, oil insulation systems, electric field management, and vacuum/altitude effects
  • Deep understanding of tube current regulation, filament and anode operation, dark current, tube aging, and tube vacuum behavior.
  • Strong understanding of switching power supplies, resonant converters, inverters, PWM systems, feedback loops, and high-voltage multipliers.
  • Advanced proficiency in evaluating manufacturing processes to maintain strict control, determine process capabilities, design assembly fixtures, and establish compliant process validation (IQ/OQ/PQ) and acceptance criteria
  • Solid understanding of cleanliness and contamination control during assembly, with specific expertise regarding fluid contamination in oil-filled assemblies
  • Application of structured reliability principles and problem-solving techniques to identify root-cause failures, evaluate field returns, and directly improve production yields.
  • Experience in verifying products that meet regulatory/safety standards, using outside test agencies.
  • Keep abreast of new products, trends, and practices within the field/scope of practice as needed
Working Conditions
  • Majority of the work is performed in a manufacturing and office environment.
  • Typical working hours and days are Monday – Friday 7am – 4pm, however this is subject to change depending on work demands
  • Periodic travel may be required (visit vendors, customers, training activities, etc.).
  • May require PPE and periodic exposure to low dose radiation.

We support a drug free work environment EOE/M/F/Disability/Vet All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.