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Medical Device Development Engineer Jobs in Massachusetts

Conflux Systems

Medical Device Test Engineer

Newton, MA · On-site

... Engineering . * 5+ years of experience in medical device testing , preferably with medical or ... Strong knowledge of verification strategy development , test method validation , and requirements ...

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Medical Device Development Engineer information

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

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 does a medical device development engineer 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 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.

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

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

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

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

Medical Device Development Engineer jobs near you
Infographic showing various Medical Device Development Engineer job openings in Massachusetts as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 12% Part Time, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution.

Product Engineer - Spinal Implant Development - Newton, MA

Michael Page USA

Newton, MA • On-site

Other

Posted 10 days ago

Job description

This role offers the opportunity to shape next‑generation spinal implant and instrument systems by translating surgeon feedback into meaningful design improvements. You will work closely with clinicians, engineers, and manufacturing partners to refine products throughout their lifecycle. Client Details My client is a growing medical device organization focused on developing advanced spinal implant technologies and surgical instrumentation. Known for its collaborative culture, the business works closely with clinical partners and leverages modern manufacturing techniques to bring innovative solutions to market, offering engineers the chance to make a tangible clinical impact. Description Reporting into the Chief Technology Officer, you will be responsible for the following: Gather, document, and organize surgeon feedback from evaluations, labs, and clinical use of spinal implants and instruments Analyze feedback to identify opportunities for design, usability, and workflow improvements Convert clinical insights into clear engineering requirements for design and R&D teams Collaborate with surgeons, internal engineers, and external manufacturing partners to assess prototypes and production tools Track design iterations and maintain detailed feedback and change documentation Support verification, validation, and usability testing activities Contribute to the development of surgical technique guides and training materials Assist with regulatory documentation, risk assessments, and design control processes Participate in cross‑functional reviews to ensure clinical input is embedded throughout development Profile Bachelor's Degree in Mechanical Engineering, Biomedical Engineering, or a related discipline At least three years' experience in medical device development within spinal products Strong understanding of surgical workflows Comfortable engaging with surgeons and multidisciplinary teams Working knowledge of CAD tools such as SolidWorks and technical documentation Familiarity with design controls, usability engineering, and risk management Exposure to additive manufacturing and FDA Class II/ISO‑regulated environments would be advantageous Proactive, detail‑oriented, and able to translate complex feedback into practical design solutions Job Offer A varied and technically engaging engineering role with real clinical exposure Opportunity to work on cutting‑edge spinal implant and instrument technologies High level of cross‑functional collaboration and visibility within the product lifecycle Professional development through hands‑on involvement in design, testing, and validation Supportive team culture within an innovative medical device organization MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.

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