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Medical Device Product Development Engineer Jobs

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Medical Device Product Development Engineer information

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$39.5K

$87.9K

$132.5K

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

As of Aug 15, 2026, the average yearly pay for medical device product development engineer in the United States is $87,884.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,000.00 and $100,000.00 per year, depending on experience, location, and employer.

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 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 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.

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

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

What states have the most Medical Device Product Development Engineer jobs?

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

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

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

Infographic showing various Medical Device Product Development Engineer 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 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $87,884 per year, or $42.3 per hour.

Senior NPI Process Development Engineer

Neptune Medical

Burlingame, CA โ€ข On-site

$140K - $175K/yr

Full-time

Retirement

Re-posted 6 days ago


Job description

Neptune Medical, is an innovative, venture capital funded medical device startup headquartered in Burlingame, CA. We have already commercialized novel medical devices using our technology. Now the team at Neptune is building something truly unique: a fully flexible medical robot that enables doctors to reach deep into human anatomy. Triton Robotic Endoscopy will disrupt flexible endoscopy and set a new standard in outcomes forย decades to come.

TITLE:ย ย Senior NPI Process Development Engineer

POSITION SUMMARY:

The Senior NPI Process Development Engineer will focus on further developing our product and then transferring it into a manufacturing setting. The successful candidate will possess a passion for medical device engineering and a record of successful process, tooling and equipment design.ย  This role will engage in cross-functional collaboration to accelerate the product development process, reduce cost of goods, and enable more complex designs through manufacturing improvements.

The ideal candidate will act with passion and intensity in a medical device start-up that is fast paced and collaborative and will display the ability to perform to the requirements outlined below. For the right person, this position will be a tremendously exciting and career-defining opportunity, making core contributions to a genuinely new type of medical robotic platform.

ROLES AND RESPONSIBILITIES:

  • Work with product development to design and prototype novel manufacturing processes and equipment
  • Develop new processes to manufacture our products to meet device performance and cost targets.
  • Design and prototype novel manufacturing equipment and fixturing
  • Create and maintain necessary Manufacturing Process Instructions (MPI's), test methods, product drawings, and component specifications
  • Upgrade our manufacturing processes to ensure proper DFM and maximum scalability of our medical devices
  • Initiate and implement programs to continuously improve quality, cost and cycle time
  • Prototype fixtures using 3-D printers, lathe, drill press, band saw, etc.
  • Provides technical support and performing failure analysis for non-conforming components, assemblies, and process defects
  • Build the assembly line for our clinical launches
  • Specify, support and maintain the proper CER space to manufacture our medical devices under defined environmental quality controls.
  • Manage the flow of WIP through Lean practices including Kanban and 5S.
  • Maintain relationships with key vendors and suppliers and support supplier validations and supplier management best practices.
  • Emphasize quality and utilize a risk-driven approach to ensure compliance to risk management policies and practices and ensure GMP.
  • Support company goals and objectives, policies and procedures that comply with FDA Quality System Regulations (QSR), ISO 13485, and any other applicable domestic regulations including Cal FDB, OSHA and Cal-OSHA.

ย REQUIRED QUALIFICATIONS:

  • B.S. or M.S. in Mechanical or Related Engineering
  • 4+ years of work experience
  • Demonstrated experience working with cross functional teams.
  • Proven track record of generating and managing manufacturing documentation from concept to commercialization for medical device product (MPIs, LHRs, BOM, flowcharts, etc.)
  • Capable with CAD modeling, engineering drawing generation, DFM, tolerance analysis and tooling design
  • Possess knowledge of process validation, GMP, and state-of-the-art manufacturing processes
  • A driven outlook and with a strong desire to succeed as an engineer, as a team, and as a company.
  • Solid understanding of design controls
  • Demonstrated success developing catheter manufacturing processes including braiding, coil winding, extruding, lamination, adhesive joining, die bonding, and laser welding.

PREFERRED QUALIFICATIONS:

  • Experience with catheter or similar manufacturing (lamination, bonding, dip coating, ultrasonic welding, etc)
  • Experience with disposables/consumables
  • Experience managing lab technicians and assemblers.
  • Developed products from invention to market release.
  • Experience in a start-up environment.
  • Proficient with SolidWorks.
  • Experience creating and managing schedules, budgets, and plans.
  • Experience with packaging and shipping validations

Neptune Medical is located in Burlingame, CA, near the Millbrae Caltrain and BART station.ย ย 

Our job titles may span more than one career level. The starting base salary for this role is between $140,000 and $175,000 depending on experience. The actual base pay is dependent upon many factors, such as: education, training, transferable skills, work experience, business needs, and location. The base pay range is subject to change and may be modified in the future. This role may also be eligible for equity, benefits and 401(K) with matching.

Neptune Medical provides equal employment opportunities to all applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.