ZipRecruiter

Log In

1

Medical Device Engineer Jobs (NOW HIRING)

Intel Corporation

Device Engineer

Hillsboro, OR · On-site

$162 - $228/hr

You will work closely with a team of engineers to push the boundaries of device performance, power ... Candidates should never be required to pay recruitment fees, medical examination fees, or any other ...

New

Excel Medical Products

Medical Device Assembly

Wixom, MI · On-site

$16 - $17/hr

Assemble medical devices and components according to engineering drawings, work instructions, and ... Prior experience in medical device assembly, electronics assembly, or precision manufacturing ...

Kellton Tech

Medical Device Assembler

Madison, WI · On-site

$23 - $24/hr

Job Title: Medical Device Assembler Location: Madison, WI (Onsite) Pay Rate: $23-24/hr on W2 ... Engineering group as required. Working Conditions: Clean, temperature controlled environment.

nLIGHT

Device Engineer

Vancouver, WA

$103K - $130K/yr

Device Engineer II: $90,000 - $115,000 * Senior Device Engineer: $103,000 to $130,000 Other ... Medical, Dental and Vision Benefits, including prescription and orthodontia with employee-paid ...

Excel Medical Products

Medical Device Assembly

Wixom, MI · On-site

$16 - $17/hr

Assemble medical devices and components according to engineering drawings, work instructions, and ... Prior experience in medical device assembly, electronics assembly, or precision manufacturing ...

Excel Medical Products

Medical Device Assembly

Wixom, MI · On-site

$16 - $17/hr

Assemble medical devices and components according to engineering drawings, work instructions, and ... Prior experience in medical device assembly, electronics assembly, or precision manufacturing ...

nLIGHT

Device Engineer

Vancouver, WA · On-site

$103K - $130K/yr

Device Engineer II: $90,000 - $115,000 * Senior Device Engineer: $103,000 to $130,000 Other ... Medical, Dental and Vision Benefits, including prescription and orthodontia with employee-paid ...

nLIGHT

Device Engineer

Vancouver, WA

$103K - $130K/yr

Device Engineer II: $90,000 - $115,000 * Senior Device Engineer: $103,000 to $130,000 Other ... Medical, Dental and Vision Benefits, including prescription and orthodontia with employee-paid ...

nLIGHT

Device Engineer

Vancouver, WA

Device Engineer II: $90,000 - $115,000 * Senior Device Engineer: $103,000 to $130,000 Other ... Medical, Dental and Vision Benefits, including prescription and orthodontia with employee-paid ...

previous page

Showing results 41-60

All JobsManufacturing JobsElectronics JobsElectronics Engineer JobsMedical Device Engineer Jobs

Medical Device Engineer information

See salary details

$21

$49

$96

How much do medical device engineer jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for medical device engineer in the United States is $49.84, according to ZipRecruiter salary data. Most workers in this role earn between $35.10 and $59.62 per hour, depending on experience, location, and employer.

What does a medical device engineer do?

A Medical Device Engineer is responsible for designing, developing, testing, and improving medical devices used in healthcare settings. They work closely with doctors, scientists, and regulatory bodies to ensure that devices are safe, effective, and compliant with industry standards. Their work includes creating prototypes, conducting risk assessments, and overseeing the manufacturing process. Medical Device Engineers play a crucial role in bringing innovative technologies to market that help diagnose, treat, or monitor medical conditions.

What does a medical device engineer do?

A medical device engineer is an engineering professional who develops new medical equipment and medical devices. As a medical device engineer, your work will vary depending on your area of expertise and may include biomedical research, material research and sourcing, computer-aided design work, and teaming up with doctors and patients. You also must understand the manufacturing process and ensure the products you design are both useful and cost-effective. You look for innovative solutions to medical problems and design new equipment diagnoses and treatments.

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

To thrive as a Medical Device Engineer, you need a solid background in biomedical, mechanical, or electrical engineering, often supported by a relevant bachelor's or master's degree. Familiarity with CAD software, regulatory standards (such as FDA or ISO 13485), and design validation tools is typically required. Strong problem-solving, communication, and teamwork skills are essential for collaborating on multidisciplinary projects and ensuring product safety. These competencies are crucial for developing innovative, compliant devices that improve patient outcomes and meet rigorous industry standards.

What are some common challenges medical device engineers face when bringing a new product from concept to market?

Medical Device Engineers often encounter challenges such as navigating complex regulatory requirements, ensuring product safety and efficacy, and coordinating with cross-functional teams including design, manufacturing, and quality assurance. Balancing innovation with compliance, managing timelines, and addressing unforeseen technical issues are also typical hurdles. Successful engineers leverage strong project management and communication skills to collaborate effectively and bring devices to market efficiently.

What is the difference between Medical Device Engineer vs Biomedical Engineer?

AspectMedical Device EngineerBiomedical Engineer
CredentialsBachelor's or Master's in Engineering, certifications in medical device designBachelor's or Master's in Biomedical Engineering or related field
Work EnvironmentDesign, develop, test medical devices in labs or manufacturing settingsResearch, develop medical equipment, or work in clinical settings
Industry UsagePrimarily in medical device manufacturing companiesHospitals, research institutions, medical device companies

Medical Device Engineers focus on designing and testing specific medical devices, ensuring compliance and safety. Biomedical Engineers have a broader scope, working on medical equipment, implants, and research. Both roles require similar credentials and often overlap in industry settings, but their primary focus differs.

More about Medical Device Engineer jobs

What cities are hiring for Medical Device Engineer jobs?

Cities with the most Medical Device Engineer job openings:

What are the most commonly searched types of Medical Device Engineer jobs?

The most popular types of Medical Device Engineer jobs are:

Who are the top companies hiring for Medical Device Engineer jobs?

The top employers for Medical Device Engineer jobs are:

What states have the most Medical Device Engineer jobs?

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

What job categories do people searching Medical Device Engineer jobs look for?

The top searched job categories for Medical Device Engineer jobs are:

What are popular job titles related to Medical Device Engineer jobs?

For Medical Device Engineer jobs, the most frequently searched job titles are:

Medical Device Engineer jobs near you
Infographic showing various Medical Device Engineer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, and 6% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $103,662 per year, or $49.8 per hour.

Device Engineer - GMP Manufacturing Support & Mechanical Testing (JP15754)

3 Key Consulting

New Albany, OH

$31 - $35/hr

Full-time

Posted 9 days ago

Job description

Job Title:   Device Engineer – GMP Manufacturing Support & Mechanical Testing (JP15754)
Location: New Albany, OH 43054
Employment Type: Contract
Business Unit: Commercial Drug Product
Duration: 1+ year (with likely extensions and/or conversion to permanent)
Posting Date: 08/20/2026
Pay Rate: $31 - $35/hour W2
Notes: Only qualified candidates need apply.  Fully Onsite (5 Days per Week) standard hours.  Potential overtime.
3 Key Consulting is hiring a  Device Engineer – GMP Manufacturing Support & Mechanical Testing for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Our ideal candidate:
  • Hands-on experience in engineering environments, particularly with tools like Instron systems and optical measurement methods
  • Proficiency in technical documentation and teamwork.
  • Hands-on experience working within a GMP manufacturing environment is required, including familiarity with GMP documentation practices, manufacturing operations, and quality systems.
  • Experience in regulated industries, preferably biopharma, biomedical, or medical devices, is strongly preferred, though aerospace or mechanical disciplines are acceptable provided the candidate also has relevant GMP manufacturing experience.
  • Proficiency in Microsoft Office is required, and CAD/SolidWorks skills are a plus.
  • Entry-level candidates with practical experience, such as internships within a GMP manufacturing or similarly regulated production environment, are preferred.

The Device Engineer will provide technical engineering support for material and component-related issues associated with commercial drug delivery devices and manufacturing operations. The primary focus of this role will be the triage, testing, investigation, escalation, and documentation of material-related issues identified during manufacturing or through other quality and technical support processes.
The engineer will work closely with Manufacturing, Quality, Engineering, and other cross-functional partners to assess reported issues, determine appropriate testing and investigation strategies, generate and review technical data, and support timely disposition or escalation of issues.
Scope includes mechanical delivery devices and associated components, including prefilled syringe systems. The qualified candidate will be part of a sustaining device engineering team supporting commercial manufacturing and product lifecycle activities. This position requires strong attention to detail, hands-on technical capabilities, and the ability to accurately document work within a GMP-regulated environment.
Why is the Position Open?
Supplement additional workload on team
Top Must Have Skills:
  • Strong Communication
  • Experience in a GMP Manufacturing Environment
  • Strong Technical Writing
  • Soft skills that need to be screened for: Looking for a self starter, someone who is ambitious

Day to Day Responsibilities:
  • Collaborate Cross-Functionally with the Various SMEs at the FDP Manufacturing Sites to Identify Device Issues and Root Causes
  • Expanding Documentation of Site Capability and Control Strategies
  • Ensuring Expedited communication to wider team on risks to device manufacturing
  • Authors and reviews technical documentation including protocols, reports, and technical assessments
  • Analyze and trend generated data by applying relevant statistical techniques to enable senior staff to make informed decisions
  • Coordinates and executes laboratory testing to support characterization, verification, design transfer, and fill-finish efforts
  • Maintains combination product design history files for assigned products
  • Develops characterization test methods through fixture prototyping, reference sample creation, and GR&R analysis
  • Provides functional subject matter expertise to actively participate in cross-functional activities including system level root cause analysis, design changes, and change control assessments
  • Provide general laboratory support including inventory management, sample shipments, and cleanup.
  • Works with Scientists and Engineers, to assess and develop appropriate design and manufacturing specifications
  • Individual contributor with Leadership attributes to effectively represent device engineer within a large network/matrix organization

Basic Qualifications:
  • Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experience
  • At a minimum familiar with the following standards and regulations:
    • Quality System Regulation – 21CFR820
    • Risk Management – ISO 14971
    • EU Medical Device requirements – Council Directive 93/42/EEC
  • Demonstrates experience working in a GMP manufacturing environment and adheres to strict GMP documentation and compliance practices
  • Fully competent engineer in all conventional aspects of the subject matter, functional area, and assignments, plans and conduct work requiring judgment in the independent evaluation, selection, and substantial adaptation and modification of standard techniques, procedures and criteria and devises new approaches to problems encountered.

Preferred Qualifications:
  • Bachelor’s Degree or higher in relevant engineering or scientific field (Mechanical, Biomedical, Bioengineering)
  • Minimum 2 years of scientific or engineering experience working in a GMP regulated manufacturing environment
  • Demonstrated understanding of GMP manufacturing operations, documentation practices, deviations/change controls, and working within an established quality system
  • Statistical Analysis software (Minitab or JMP)
  • Strong technical writing skills
  • CAD fixturing software (SolidWorks)
  • Tolerance Stack-Ups (2D, 3D, RSS)
  • Instron force tester using BlueHill Universal
  • CT-Scanning
  • Deviations and CAPAs
  • Experience with design controls; including (but not limited to) verification and design transfer
  • Understanding of risk assessments including hazard and probability analysis
  • Background in medical device development, commercialization and knowledge of manufacturing processes (fill-finish)
  • Ability to work independently and dynamically across functional teams
  • Excellent written and verbal communication skills
  • Ability to support complex workstreams under demanding timelines

Employee Value Proposition:
Unique industry opportunity, industry experience
Red Flags:
  • No Cross-Functional Experience
  • No Practical Work Experience

Interview process:
Initial 1:1 Phone Interview with Hiring Manager
Group Interview with CORE SMEs
We invite qualified candidates to send your resume to resumes@3keyconsulting.com.  If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.