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Medical Device Development Engineer Jobs (NOW HIRING)

TIDI Products

Product Development Engineer

Lincolnshire, IL · On-site +1

$80K - $95K/yr

The Product Development Engineer is responsible for product development within TIDI Products ... Experience in medical device under FDA 21 CFR 820.30 Design Controls, ISO 13485 and ISO 14971 Risk ...

Spyglass Pharma

Senior Engineer, R&D

Aliso Viejo, CA · On-site

$110.60K - $151.80K/yr

Maintain up-to-date knowledge of relevant industry trends, engineering tools, and best practices in medical device development. Qualifications Required For Position: * 4-5 years of engineering ...

Spyglass Pharma

Senior Engineer, R&D

Aliso Viejo, CA

$110.60K - $151.80K/yr

Maintain up-to-date knowledge of relevant industry trends, engineering tools, and best practices in medical device development. Qualifications Required For Position: * 4-5 years of engineering ...

Spyglass Pharma

Senior Engineer, R&D

Aliso Viejo, CA · On-site

$120K - $140K/yr

Maintain up-to-date knowledge of relevant industry trends, engineering tools, and best practices in medical device development. Qualifications Required For Position: * 4-5 years of engineering ...

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Medical Device Development Engineer information

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

As of May 29, 2026, the average yearly pay for medical device development engineer in the United States is $96,155.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,500.00 and $106,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Medical Device Development Engineer, and why are they important?

To thrive as a Medical Device Development Engineer, you need a solid background in biomedical, mechanical, or electrical engineering, often with a relevant degree and experience in product development. Familiarity with CAD software, regulatory standards (like ISO 13485 and FDA requirements), and prototyping tools is typically required. Strong problem-solving abilities, attention to detail, and effective teamwork and communication skills help you excel in multidisciplinary environments. These competencies are vital to ensure medical devices are safe, effective, and compliant with industry regulations.

How do Medical Device Development Engineers typically collaborate with cross-functional teams during the product development process?

Medical Device Development Engineers frequently work alongside professionals from regulatory, quality assurance, manufacturing, and clinical teams to bring products from concept to market. This collaboration ensures that devices are designed for manufacturability, meet regulatory requirements, and address user needs. Regular meetings, design reviews, and documentation exchanges are common, making strong communication and teamwork skills essential for success in the role.

What does a Medical Device Development Engineer do?

A Medical Device Development Engineer is responsible for designing, developing, and testing medical devices used in healthcare settings. They work closely with doctors, regulatory agencies, and manufacturing teams to ensure devices are safe, effective, and compliant with regulations. Their tasks often include creating prototypes, running experiments, analyzing data, and preparing documentation for regulatory approval. This role requires a strong background in engineering, biology, or materials science, as well as knowledge of medical industry standards.

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

AspectMedical Device Development EngineerBiomedical Engineer
CredentialsBachelor's or Master's in Engineering, certifications in medical device regulationsBachelor's or Master's in Biomedical Engineering or related field
Work EnvironmentDesign labs, R&D departments, manufacturing settingsHospitals, research labs, medical device companies
Industry UsageFocuses on designing and developing medical devicesBroader scope including medical equipment, implants, and healthcare technology

Medical Device Development Engineers primarily focus on designing and developing medical devices, working closely with engineering and regulatory teams. Biomedical Engineers have a broader role, often involved in research, testing, and improving medical equipment and healthcare technologies. While both roles require engineering credentials and may work in similar environments, their specific responsibilities and focus areas differ.

More about Medical Device Development Engineer jobs
What states have the most Medical Device Development Engineer jobs? States with the most job openings for Medical Device Development Engineer jobs include:
What job categories do people searching Medical Device Development Engineer jobs look for? The top searched job categories for Medical Device Development Engineer jobs are:
Medical Device Development Engineer jobs near you
Infographic showing various Medical Device Development Engineer job openings in the United States as of May 2026, with employment types broken down into 1% Internship, 2% As Needed, 12% Full Time, 76% Part Time, 1% Temporary, and 8% Contract. Highlights an 36% Physical, 9% Hybrid, and 55% Remote job distribution, with an average salary of $96,155 per year, or $46.2 per hour.
Engineer Senior, Drug Delivery Medical Device - (JP9675)

Engineer Senior, Drug Delivery Medical Device - (JP9675)

3 Key Consulting

Thousand Oaks, CA

$110.60K - $151.90K/yr

Other

Posted 7 days ago

Job description

Job Title: Engineer Senior, Drug Delivery Medical Device - (JP9675)
Location: Thousand Oaks, CA.
Employment Type: Contract
Business Unit: Mechanical Autoinjectors Platform
Duration: 1+ years (with likely extensions and/or conversion to permanent)
Posting Date: 1/13/2022
Notes:
3 Key Consulting is hiring an Engineer Senior for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Support the teams in the development of drug delivery devices. Scope includes a wide range of devices, such as; needle protection systems, fluid transfer devices, pen injectors, automatic pen injectors, and micro-infuser delivery pump systems. The qualified candidate will support technical teams to ensure successful device development of these mechanical and electro-mechanical medical devices. The Sr. Engineer will work closely with device Subject Matter Expert (SME) to support develop detailed engineering specifications, device design & development, support verification, validation, and regulatory submissions of these devices. The role of the Sr. Engineer is to work within a cross-functional organization to utilize technologies and methodologies that support short-cycle robust device development. Responsibilities include:
  • Work cross-functionally with individuals and project teams in Quality, Operations, and Development.
  • Create and assess product requirements to determine technical coverage and proper integration different subsystems.
  • Execute to project plans and schedules.
  • Develop, execute, and review architecture documents, design documents, specifications, development plans, characterization plan, verification and validation plans and other related product development documents for assigned projects.
  • Provide technical assistance for junior engineers.

Why is the Position Open?
Supplement additional workload on team
Top Must Have Skills:
1. 5 years min experience in device engineering end to end configuration control management
2. Design characterization, verification execution.
3. Device design experience(design for six sigma experience a +)
Day to Day Responsibilities:
Support and manage day to day commercial advancement operation to ensure deliverables and deadlines are met. Coordinate activities and provide guidance to jr. engineers
Basic Qualifications:
  • BS in Engineering and previous experience in a medical device industry.
  • 10 years current experience with engineering processes and procedures.
  • Strong background in engineering and commercialization of electro-mechanical medical devices.
  • Experience with material & test specs generation, protocol & report writing, process & test development, prototyping, design verification, DOE/SPC process optimization & validation (IQ, OQ, PQ), FMEA.
  • Product design/development (design control).
  • Experience in drug/device combination product design and development.
  • Familiar with the following standards:
    • Quality System Regulation 21CFR820 - Risk Management; ISO 14971 - EU Medical Device requirements; Council Directive 93/42/EEC - Medical Electrical Equipment; EN 60601 - Small scale device assembly experience.
  • Ability to read, analyze, and interpret general technical procedures, or governmental regulations.
  • Strong problem solving, risk assessment, and risk management skills.
  • Must be capable of working on multiple projects in a deadline driven environment.
  • VERY IMPORTANT NOTE: Qualified candidates with either a strong Electrical Engineering, Mechanical Engineering, OR Systems Engineering background need apply and will be considered!!!

Employee Value Proposition:
Great biotech/pharma to work for.
Red Flags:
Applicants without 5 years of experience with one company.
Interview process:
Video Skype Panel Interview
We invite qualified candidates to sendyour resume toresumes@3keyconsulting.com. Ifyou decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our websitewww.3keyconsulting.com/careers. You are also welcome to sharethis opportunity withanyone you think might be interested in applying for this role.

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