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Medical Device Product Development Engineer Jobs in California

Product Development Engineer II

Irvine, CA · On-site

$71K - $97K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Bachelor's Degree in Engineering (or equivalent) required. * 3-5 years of related experience in medical device product development. * Proficiency with CAD software (e.g., SolidWorks). * Demonstrated ...

Product Development Engineer II

Irvine, CA

$71K - $97K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Bachelor's Degree in Engineering (or equivalent) required. * 3-5 years of related experience in medical device product development. * Proficiency with CAD software (e.g., SolidWorks). * Demonstrated ...

Product Development Engineer

Milpitas, CA · On-site

$117K - $200K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Virtually every electronic device in the world is produced using our technologies. No laptop ... medical, dental, vision, life, and other voluntary benefits, 401(K) including company matching ...

Product Development Engineer

Thousand Oaks, CA · On-site

$98K - $120K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

Minimum 2 years' experience in product development; medical device or another highly regulated industry is highly preferred * Proficient in 3D CAD modeling and Engineering Drawings (SolidWorks or ...

Showing results 21-40

Medical Device Product Development Engineer information

See California salary details

$39K

$86.7K

$130.8K

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

As of Aug 17, 2026, the average yearly pay for medical device product development engineer in California is $86,733.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,100.00 and $98,700.00 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 California?

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

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

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

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

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

Infographic showing various Medical Device Product Development Engineer job openings in California 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 $86,733 per year, or $41.7 per hour.

Senior Product Development Engineer I

Integra LifeSciences

Irvine, CA • On-site, Remote

$81K - $112K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 19 days ago


Integra LifeSciences rating

9.4

Company rating: 9.4 out of 10

Based on 9 frontline employees who took The Breakroom Quiz


Job description

Changing lives. Building Careers.

Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what's possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.

The Senior Product Development Engineer I will play a critical leadership role in the full lifecycle development of innovative ENT (Ear, Nose, and Throat) medical devices at Integra - from concept through commercial release. This position leads technical aspects of projects while supporting cross-functional teams in design, design for manufacturability (DFM), test method development, verification, validation, and usability testing. The ideal candidate is a hands-on technical leader with strong business acumen who can drive complex projects and mentor team members in a regulated medical device environment.

Key Responsibilities

  • Design and develop ENT medical devices and related accessories (e.g., cables, sheaths, suctions, balloons).
  • Interface with external vendors to develop and procure components; proactively resolve design challenges related to materials, specifications, tolerances, service requirements, manufacturing processes, and cost.
  • Develop tools, jigs, and fixtures to support prototyping, manufacturing, and testing activities.
  • Create preliminary sketches and detailed design concepts; perform measurements, analyses, and produce engineering prototypes.
  • Develop and execute engineering tests (benchtop, verification & validation (V&V), pre-clinical, and usability); author detailed protocols and comprehensive reports.
  • Gather Voice of the Customer (VOC) input from physicians and end-users to inform product requirements and improvements.
  • Lead technical reviews, including design reviews and technical assessments.
  • Recommend, design, and/or purchase equipment needed for development and testing.
  • Communicate project status, risks, business-related issues, and opportunities effectively to the next level of management.
  • Ensure compliance with all applicable federal, state, and local regulations, as well as company policies related to Health, Safety, and Environmental practices.
  • Perform other duties as assigned.

Qualifications & Requirements

  • Bachelor's degree in engineering (or equivalent) required.
  • At least 4 years of related experience in medical device product development.
  • Proficiency with CAD software (e.g., SolidWorks).
  • Demonstrated ability to lead technical teams.
  • Strong verbal and written communication skills, with solid experience in project management methodology, problem-solving, and presentations.
  • Strong business acumen and the ability to collaborate effectively with all levels of management in a cross-functional team environment.
  • Proficiency in Microsoft Office applications (Word, Excel, PowerPoint).
  • Mechanical Engineering degree preferred.
  • Working knowledge of design controls, risk management (ISO 14971), production and process controls, and relevant regulatory standards (ISO 13485, FDA Quality System Regulation).
  • Experience with statistical analysis software (e.g., Minitab), process mapping (Visio), and project management tools (Microsoft Project).
  • Travel: Up to 25%.
  • Work Environment: Office, Remote, or Hybrid.

    Salary Pay Range:

    $81,650.00 - $112,700.00 USD Salary

    Our salary ranges are determined by role, level, and location. Individual pay is determined by several factors including job-related skills, experience, and relevant education or training. In addition to base pay, employees may be eligible for bonus, commission, equity or other variable compensation. Your recruiter can share more about the specific salary range for your preferred location during the hiring process.

    Additional Description for Pay Transparency:

    Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance, and savings plan (401(k)).

    Subject to the terms of their respective policies and date of hire, Employees are eligible for the following Total Rewards | Integra LifeSciences

    Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status.
    This site is governed solely by applicable U.S. laws and governmental regulations. If you'd like more information on your rights under the law, please see the following notices:
    EEO Is the Law | EOE including Disability/Protected Veterans
    Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA. If you have difficulty using our online system due to a disability and need an accommodation, please email us at careers@integralife.com.

    Unsolicited Agency Submission

    Integra LifeSciences does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. A formal written agreement is required before engaging any agency, and it must be executed and authorized by the Vice President, Talent Acquisition. Where agency agreements are in place, introductions (the initial sharing of a candidate's name, resume, or background) are position-specific and may only occur within the scope of that approved agreement. Please, no phone calls or emails.

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