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Mechanical Engineer Medical Devices Jobs (NOW HIRING)

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Mechanical Engineer Medical Devices information

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$45.5K

$102.9K

$166.5K

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

As of Sep 6, 2026, the average yearly pay for mechanical engineer medical devices 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 in medical devices?

Mechanical engineers in medical devices are professionals who design, develop, and test mechanical components and systems used in medical equipment and devices. They apply engineering principles to ensure devices like implants, diagnostic machines, and surgical instruments are safe, reliable, and effective. Their role often involves working closely with other engineers, medical professionals, and regulatory experts to meet strict safety and performance standards. They also contribute to the improvement and innovation of medical technology to enhance patient care.

What are some common challenges faced by mechanical engineers working in the medical device industry?

Mechanical engineers in the medical device industry often face the challenge of balancing strict regulatory requirements with innovative design. Ensuring that products meet FDA or international standards while maintaining functionality and cost-effectiveness can be complex. Collaboration with cross-functional teams, including regulatory, manufacturing, and clinical experts, is crucial to address technical and compliance issues. Additionally, rapid prototyping and testing are frequently required to iterate designs efficiently while keeping patient safety paramount.

What are the key skills and qualifications needed to thrive as a mechanical engineer in medical devices, and why are they important?

Mechanical Engineers in Medical Devices require expertise in mechanical design, materials science, and a relevant engineering degree, often with experience in biomedical applications. Familiarity with CAD software (such as SolidWorks), regulatory standards (like FDA and ISO 13485), and design control systems is vital. Strong problem-solving, attention to detail, and effective teamwork elevate performance in this highly regulated field. These skills and qualifications ensure the development of safe, innovative, and compliant medical devices that improve patient outcomes.

What is the difference between Mechanical Engineer Medical Devices vs Mechanical Engineer Medical Devices?

AspectMechanical Engineer Medical Devices
CertificationsTypically requires a Bachelor's degree in Mechanical Engineering; certifications like Certified Manufacturing Engineer (CMfgE) are common
Work EnvironmentDesign labs, manufacturing facilities, quality assurance departments
Industry UsageMedical device manufacturing, research, and development
Job FocusDesign, develop, and test medical devices such as surgical tools, implants, and diagnostic equipment

Both roles involve designing and developing medical devices, requiring similar credentials and work environments. The primary difference lies in specific project focus and application areas within the medical device industry.

More about Mechanical Engineer Medical Devices jobs

What cities are hiring for Mechanical Engineer Medical Devices jobs?

Cities with the most Mechanical Engineer Medical Devices job openings:

What states have the most Mechanical Engineer Medical Devices jobs?

States with the most job openings for Mechanical Engineer Medical Devices jobs include:

Infographic showing various Mechanical Engineer Medical Devices 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 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $102,878 per year, or $49.5 per hour.

Principal Mechanical Engineer (Medical Devices)

AA2IT

Raleigh, NC • On-site

$55 - $65/hr

Full-time

This job post has expired today. Applications are no longer accepted.


Job description

Req ID: HCR0003122
Title: Principal Mechanical Engineer (Medical Devices)
Location: 6501 Six Forks Rd. Raleigh, NC 27615
Pay Rate: $55-$65/HR on W2

Overview

The Principal Mechanical Engineer will develop new products, redesign existing products, and conduct research and testing on product concepts related to medical devices. This role is a key member of the driving innovation, development, verification, and transfer to manufacturing in support of Merz business objectives.

The successful candidate must have experience in a medical device company and be fully familiar with regulatory and quality requirements across all stages of the product development lifecycl

Minimum Qualifications

  • Bachelor's degree in Mechanical, Industrial, Electrical Engineering or a related discipline
  • 10+ years design and manufacturing experience in the medical device or component development industry
  • Proven Design Controls experience, including design verification and validation
  • Strong background in manufacturing and assembly process development and validation (IQ/OQ/PQ)

Hands-on experience with prototype development, test method development, and manufacturing scale-up

Responsibilities

1. Technical Lead

  • Provide technical leadership of system features and functions for medical devices.
  • Lead cross-functional engineering groups through collaboration and technical influence.
  • Serve as subject matter expert in mechanical design, test methods, and system-level decisions.
  • 2. Mechanical Engineering & Project Leadership
  • Lead advanced development projects; manage team members to ensure on-time execution.
  • Deliver engineering analyses, feasibility studies, and detailed technical assessments.
  • Provide broad mechanical engineering expertise across concept, design, verification, and transfer-to-manufacturing phases.
  • Oversee design and process V&V activities in accordance with Design Controls.
  • 3. Innovation
  • Develop, design, and test Client concepts and solutions aligned with clinical, patient, and business needs.
  • Collaborate with engineering and marketing teams on technical feasibility.
  • Design and build test setups, fixtures, and prototypes for advanced development initiatives.
  • 4. Documentation
  • Maintain compliant, accurate documentation following GDP and GMP standards.
  • Author product requirements, specifications, and technical documentation.
  • Plan, design, execute, and report system experiments aligned with feature development and the product roadmap.
  • 5. Test Methods
  • Create and execute test plans to prove and refine product designs.
  • Perform performance calculations, design adjustments, and prototype evaluations.
  • Validate test tools, fixtures, and setups per regulatory and quality expectations.

Ensure all testing complies with FDA, ISO, and internal quality system requirements.

Kindly share your resume with answers:
Q1: How many years of exp in design and manufacturing experience in the medical device or component development industry
Q2: How many years of exp in Design Control experience including design and process verification and validation
Q3: How soon you are ready to start and what is your present salary