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Medical Device Product Development Engineer Jobs in Massachusetts

Cardinal Health, Inc.

$73.20 - $94.23/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

This entry-level positionis responsible forplanning, developing, executing, and documenting engineering tests in support of medical device product development and sustaining engineering efforts. The ...

New

Jobtailor

Director, Product Manager Type 2

Acton, MA · On-site

$150 - $190/hr

Medical Device * Class II+ Medical Device * Product Development Lifecycle * Regulatory Compliance * Human Factors Engineering Tools & Technologies * Agile Tools * User-Experience Research Tools

New

SharkNinja

Senior Medical Device Compliance Engineer

Needham, MA · On-site

$113K - $156K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

This role is hands-on and central to ensuring medical device products are developed and sustained ... Bachelor's or Master's degree in Engineering (Mechanical, Electrical, Biomedical), Quality, or a ...

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Showing results 1-20

All JobsMedical Device Product Development Engineer JobsMedical Device Product Development Engineer Jobs in Massachusetts

Medical Device Product Development Engineer information

See Massachusetts salary details

$43.1K

$96K

$144.7K

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

As of Aug 19, 2026, the average yearly pay for medical device product development engineer in Massachusetts is $95,980.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,600.00 and $109,200.00 per year, depending on experience, location, and employer.

What does a medical device product development engineer do?

A Medical Device Product Development Engineer is responsible for designing, developing, and testing medical devices to ensure they are safe, effective, and compliant with regulatory standards. They work closely with cross-functional teams, including quality assurance, regulatory affairs, and manufacturing, to take products from concept through to production. Their tasks often include prototyping, risk assessment, documentation, and troubleshooting any issues that arise during the development process. Additionally, they must stay updated on industry standards and regulations to ensure that products meet all necessary requirements for market approval.

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

To thrive as a Medical Device Product Development Engineer, you need a strong background in biomedical, mechanical, or electrical engineering, along with knowledge of FDA regulations and product development processes. Familiarity with CAD software, prototyping tools, risk management systems, and regulatory standards such as ISO 13485 is typically required. Creativity, problem-solving, and effective teamwork are essential soft skills that drive innovation and ensure project success. These skills and qualifications are crucial for developing safe, effective medical devices that meet strict regulatory requirements and address real-world healthcare needs.

What are some common challenges medical device product development engineers face when working on new product designs?

Medical Device Product Development Engineers often navigate strict regulatory requirements and rigorous testing protocols to ensure product safety and compliance. Balancing innovative design with manufacturability and cost constraints can be challenging, as can coordinating input from cross-functional teams such as clinical, regulatory, and manufacturing. Additionally, managing project timelines while accommodating iterative design changes based on feedback or testing results requires strong organizational and communication skills.

What is the difference between Medical Device Product Development Engineer vs Quality Assurance Engineer?

AspectMedical Device Product Development EngineerQuality Assurance Engineer
CredentialsEngineering degree, certifications like PMP or Six Sigma often preferredEngineering or science degree, certifications like CQE or ISO auditor training
Work EnvironmentDesign labs, R&D departments, cross-functional teamsManufacturing facilities, quality control labs, compliance departments
Industry UsageInvolved in designing and developing new medical devicesEnsures products meet quality standards and regulatory requirements

While both roles are essential in the medical device industry, the Medical Device Product Development Engineer focuses on creating and improving devices, whereas the Quality Assurance Engineer ensures these devices meet safety and quality standards. Understanding these differences helps in choosing the right career path or job search focus.

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

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

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

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

What cities in Massachusetts are hiring for Medical Device Product Development Engineer jobs?

Cities in Massachusetts with the most Medical Device Product Development Engineer job openings:

Medical Device Product Development Engineer jobs near you
Infographic showing various Medical Device Product 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, with an average salary of $95,980 per year, or $46.1 per hour.

Interventional Device Development Engineer

Theragenics Corp

Attleboro Falls, MA • On-site

$105K - $165K/yr

Full-time

Re-posted 25 days ago

Job description

Compensation:

  • 2–5 years of experience: Starting at $105,000
  • 6–9 years of experience: Progressively higher based on experience, skills, and performance
  • 10+ years of experience: Up to $165,000


Be part of a mission that matters—join Arrotek, a Theragenics company, as a Senior Interventional Device Development Engineer and help bring innovative medical technologies from concept to commercialization. In this critical role, you'll lead the design, development, optimization, and transfer of advanced interventional medical devices, including catheter and guidewire technologies that improve patient outcomes worldwide.

Working alongside multidisciplinary engineering teams, manufacturing experts, and global clients, you'll play a key role in developing life-changing solutions that enable physicians to perform safer, less invasive procedures. If you're passionate about innovation, technical excellence, and making a meaningful impact in healthcare, this is your opportunity to help shape the future of medical technology.

Company Overview

At Theragenics, we're passionate about transforming healthcare and enhancing patient outcomes. Our commitment to innovation drives us to push the boundaries of what's possible, ensuring a brighter future for patients everywhere.

Theragenics is a leader in developing medical devices focused on minimally invasive treatments for cancer, vascular interventions, and surgical applications. Headquartered in Atlanta, Georgia, the company operates facilities in Costa Rica, Texas, and Massachusetts.

Theragenics proudly operates Arrotek, a leading medical device design and development consultancy with locations in the United States and Ireland. Arrotek specializes in pioneering minimally invasive technologies that improve lives through innovative engineering, product development, and manufacturing solutions.

Role Summary

As a Senior Interventional Device Development Engineer, you will apply advanced engineering expertise to lead the development of innovative interventional medical devices from concept through commercialization. You will serve as a technical leader across development programs, mentor junior engineers, collaborate directly with clients, and drive the successful execution of complex product and process development projects in a highly regulated environment.

Key Responsibilities
  • Lead the design and development of interventional medical devices, including catheters, guidewires, and electromechanical systems.
  • Generate innovative concepts and evaluate designs through engineering analysis, prototyping, testing, and design reviews.
  • Develop, optimize, and validate manufacturing and assembly processes, including extrusion, reflow, tipping, bonding, laser processing, and precision assembly.
  • Execute and lead Design of Experiments (DOE), feasibility studies, verification, and validation activities.
  • Conduct risk assessments, FMEA activities, and design control reviews throughout the product lifecycle.
  • Develop and maintain technical documentation including DHFs, DMRs, BOMs, drawings, protocols, and engineering reports.
  • Lead technical workstreams and support project planning, scheduling, budget management, and deliverable execution.
  • Interface directly with customers to communicate project status, technical recommendations, and development strategies.
  • Mentor and provide technical guidance to junior engineers and project team members.
  • Collaborate with Quality, Regulatory, Manufacturing, Supply Chain, and external partners to ensure successful product development and commercialization.
  • Support manufacturing transfer, process scale-up, root cause investigations, and continuous improvement initiatives.
  • Ensure compliance with FDA, ISO 13485, ISO 14971, MDR, and applicable regulatory requirements.
Qualifications & SkillsRequired Qualifications
  • Bachelor's degree in Biomedical, Mechanical, Manufacturing, Plastics, Polymer Engineering, or a related engineering discipline.
  • 5–10 years of experience in medical device product development, preferably focused on catheter, guidewire, or minimally invasive technologies.
  • Demonstrated experience leading technical development activities within a regulated medical device environment.
  • Strong knowledge of design controls, risk management, verification and validation, and product lifecycle management.
  • Experience developing and optimizing manufacturing processes for medical devices.
  • Excellent technical communication, project leadership, and problem-solving skills.
Preferred Qualifications
  • Master's degree in Engineering or related technical field.
  • Experience within a contract design and manufacturing organization (CDMO) environment.
  • Expertise in catheter or guidewire development technologies.
  • Experience with customer-facing engineering and project leadership.
  • Strong knowledge of FDA, ISO 13485, and MDR requirements.
Core CompetenciesTechnical Competencies
  • Medical Device Product Development
  • Catheter & Guidewire Engineering
  • Design Controls & Product Lifecycle Management
  • Design for Manufacturability (DFM)
  • Design of Experiments (DOE)
  • Verification & Validation (V&V)
  • Risk Management & FMEA
  • Process Development & Optimization
  • Manufacturing Transfer & Scale-Up
  • Prototype Development & Testing
  • Statistical Analysis & Data Interpretation
  • Root Cause Analysis & Problem Solving
  • Technical Documentation
  • FDA & ISO 13485 Compliance
Leadership Competencies
  • Technical Leadership
  • Coaching & Mentoring
  • Stakeholder Management
  • Influencing Without Authority
  • Cross-Functional Collaboration
  • Strategic Thinking
  • Customer Focus
  • Innovation & Continuous Improvement
  • Program Awareness
  • Results Orientation
Why Join Us?
  • Lead cutting-edge medical device development programs that directly impact patient care.
  • Collaborate with industry-leading engineers, clinicians, and global customers.
  • Work on innovative catheter and guidewire technologies from concept through commercialization.
  • Expand your technical leadership and career growth opportunities.
  • Be part of a highly collaborative and mission-driven culture.
  • Receive competitive compensation and comprehensive benefits.

“We don’t just develop devices; we create solutions that help clinicians improve and extend lives.”

Apply