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Medical Device Designer Jobs in California (NOW HIRING)

Sr Medical Device Engineer

San Diego, CA ยท On-site

$110K - $152K/yr

Hands-on experience designing and optimizing manufacturing equipment and fixtures, including use of ... Medical device manufacturing experience strongly preferred. Additional Skills & Qualifications

Sr Medical Device Engineer

San Diego, CA ยท On-site

$110K - $152K/yr

Hands-on experience designing and optimizing manufacturing equipment and fixtures, including use of ... Medical device manufacturing experience strongly preferred. Additional Skills & Qualifications

Be Seen First

Senior Mechanical Engineer - Medical Device San Diego, CA (Onsite) 130,000-180,000 DOE Join a ... You'll take designs and features from concept through production, balancing new development with ...

This is a high-impact, full-time role where you'll shape the future of a product designed to ... Familiarity with medical device standards (ISO 13485, IEC 62304) Why This Role You'll join a highly ...

Graphic Designer

Santa Rosa, CA ยท On-site

$40 - $45/hr

Medical Device Manufacturing Company Duration: 12 Months (possible extension) Location: Santa Rosa, CA 95403 Shift: 1st Shift Top Requirements * Graphic design experience * Medical device/pharma ...

... medical device development projects starting from technology exploration, product definition, to ... Support cross-functional Design Transfer process to ensure product designs manufacturable ...

Develops global medical device labeling components, including carton artwork, technical information ... Designs may integrate typographic, photographic, illustrative, and graphic elements. * Works with ...

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Showing results 1-20

Medical Device Designer information

See California salary details

$74.5K

$126.6K

$185.5K

How much do medical device designer jobs pay per year?

As of Sep 2, 2026, the average yearly pay for medical device designer in California is $126,577.00, according to ZipRecruiter salary data. Most workers in this role earn between $108,600.00 and $142,100.00 per year, depending on experience, location, and employer.

What does a medical device designer do?

A Medical Device Designer is responsible for creating and developing medical devices and equipment used in healthcare settings. They combine knowledge of engineering, biology, and design principles to ensure products are safe, effective, and user-friendly. Their role involves working closely with healthcare professionals, conducting research, prototyping, and adhering to regulatory standards throughout the design and development process. Medical Device Designers help bring innovative medical solutions to market that improve patient care and outcomes.

What are the key skills and qualifications needed to thrive as a medical device designer?

To thrive as a Medical Device Designer, you need a strong background in biomedical engineering, product design, and knowledge of regulatory standards, typically supported by a relevant engineering degree. Proficiency with CAD software, rapid prototyping tools, and familiarity with FDA or ISO regulatory systems is essential. Creativity, problem-solving, collaboration, and attention to detail are vital soft skills for innovating and ensuring safety in device development. These skills and qualities are crucial for creating effective, compliant, and user-friendly medical devices that improve patient outcomes and meet industry standards.

What are some common challenges faced by medical device designers when balancing innovation with regulatory compliance?

Medical device designers often face the challenge of creating innovative, user-friendly products while ensuring strict adherence to regulatory standards such as FDA or ISO requirements. Balancing creativity with compliance can be demanding, as any design change may necessitate additional documentation, testing, and validation. Designers must closely collaborate with regulatory specialists, engineers, and clinicians to ensure their solutions are both safe and effective. Staying up-to-date with changing regulations and incorporating feedback from multidisciplinary teams are key aspects of overcoming these challenges.

What are popular job titles related to Medical Device Designer jobs in California?

For Medical Device Designer jobs in California, the most frequently searched job titles are:

What job categories do people searching Medical Device Designer jobs in California look for?

The top searched job categories for Medical Device Designer jobs in California are:

Infographic showing various Medical Device Designer job openings in California as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, and 5% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $126,577 per year, or $60.9 per hour.

Sr Medical Device Engineer

Actalent

San Diego, CA โ€ข On-site

$110K - $152K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post hasย expired 1 day ago.ย Applications are no longer accepted.


Job description

Job Title: Senior Medical Device Engineer

Job Description

The Senior Medical Device Engineer supports the development and scale-up of innovative medical device manufacturing processes and equipment from concept through pilot manufacturing and into full-scale production. In this role, you design and optimize equipment, fixtures, assembly processes, and operating procedures within a regulated quality system, ensuring robust, scalable, and compliant manufacturing solutions. You work closely with R&D and Pilot Manufacturing teams to implement new technologies and processes that directly influence how future wearable medical devices are built.

Responsibilities

  • Lead process development activities from early concept through pilot manufacturing and production scale-up.
  • Design and optimize manufacturing equipment, fixtures, assembly processes, and operating procedures within a regulated quality system.
  • Perform process characterization and execute design of experiments (DOE) to understand and optimize critical process parameters.
  • Conduct material qualification activities to ensure materials meet performance and regulatory requirements.
  • Lead root cause investigations to resolve process and equipment issues and implement effective corrective actions.
  • Provide technical oversight of pilot production builds, ensuring processes, equipment, and documentation are properly implemented.
  • Drive risk mitigation efforts related to new equipment, processes, and manufacturing technologies.
  • Validate equipment performance and support process validation activities for medical device manufacturing.
  • Manage engineering projects and timelines independently, ensuring milestones and deliverables are met.
  • Transfer technologies from development to manufacturing, including R&D, pilot manufacturing, and production scale-up activities.
  • Release equipment specifications and engineering drawings to support manufacturing and maintenance teams.
  • Develop calibration and preventative maintenance programs for manufacturing equipment and fixtures.
  • Train operators, technicians, and manufacturing personnel on new equipment, processes, and procedures.
  • Turn ambiguous manufacturing challenges into structured, well-defined processes and documentation.
  • Support high-volume manufacturing processes and continuous process improvements as needed.
  • Collaborate cross-functionally with process engineers, mechanical engineers, technicians, and operators in a fast-paced environment.
  • Mentor and support manufacturing personnel, fostering strong technical understanding and adherence to best practices.
  • Perform testing, data analysis, and capability analysis to monitor process performance and drive optimization.
  • Contribute to a high-visibility R&D engineering team focused on next-generation manufacturing technologies for wearable medical devices.

Essential Skills

  • Bachelor’s degree in Engineering or a related technical discipline.
  • 5–8 years of engineering experience, preferably in process or equipment development.
  • Hands-on experience designing and optimizing manufacturing equipment and fixtures, including use of SolidWorks.
  • Demonstrated experience executing design of experiments (DOE) and validating equipment performance.
  • Proven ability to perform root cause investigations and implement process improvements.
  • Experience moving products from R&D through pilot manufacturing and into production scale-up.
  • Ability to independently manage engineering projects, priorities, and timelines.
  • Experience working in regulated development environments, ideally medical device.
  • Strong technical problem-solving and troubleshooting skills in manufacturing and process development settings.
  • Ability to work effectively in ambiguous and fast-paced environments while maintaining high quality standards.
  • Experience transferring technologies from development to manufacturing and supporting scale-up activities.
  • Excellent verbal and written communication skills for cross-functional collaboration and training.
  • Strong attention to detail and organizational skills in documentation and execution.
  • Demonstrated hands-on engineering experience in equipment, process, or manufacturing development.
  • Experience supporting high-volume manufacturing processes.
  • Experience releasing equipment specifications and engineering drawings.
  • Experience developing calibration and preventative maintenance programs for manufacturing equipment.
  • Experience training operators and manufacturing personnel on new processes and equipment.
  • Ability to translate ambiguous manufacturing challenges into structured, repeatable processes.
  • Experience supporting R&D, pilot manufacturing, and production scale-up activities.
  • Medical device manufacturing experience strongly preferred.

Additional Skills & Qualifications

  • Mechanical Engineering, Biomedical Engineering, or Biomechanical Engineering degree preferred.
  • Experience with SolidWorks for equipment and fixture design.
  • Experience with statistical tools such as JMP and Minitab for DOE, capability analysis, and data interpretation.
  • Material characterization and process validation in a regulated environment.
  • Familiarity with capability analysis and other statistical methods for monitoring and improving process performance.
  • Comfort working in ambiguous environments and defining structure where processes are still evolving.
  • Strong collaboration skills for working with engineers, operators, and technicians across R&D and manufacturing.
  • Interest in next-generation manufacturing technologies for wearable medical devices.
  • Motivation to work in a high-visibility R&D engineering team with contract-to-hire potential.

Work Environment

This is a fully onsite role at an R&D and pilot manufacturing campus in San Diego, working standard business hours (8:30 AM–5:30 PM) with occasional overtime based on business needs. You operate in a regulated medical device development and manufacturing environment, with a combination of laboratory work, pilot production activities, equipment development, testing, and data analysis. The role is highly hands-on, supporting process development, equipment development, and manufacturing scale-up activities. You collaborate daily with a growing team of approximately 4–5 engineers, as well as process engineers, mechanical engineers, technicians, and operators. The environment emphasizes cross-functional teamwork, mentorship, and training of manufacturing personnel, providing broad exposure to product development from concept through pilot manufacturing and into full-scale production.

Job Type & Location

This is a Contract position based out of San Diego, CA.

Pay and Benefits

The pay range for this position is $55.00 - $65.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in San Diego,CA.

Application Deadline

This position is anticipated to close on Sep 4, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law.

If you would like to request a reasonable accommodation, such as the modification oradjustment of the job application process or interviewing process due to a disability,please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance:Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in thecity and county of San Francisco, we will consider for employment qualified applicantswith arrest and conviction records.

Massachusetts Lie Detector:It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):We may use Artificial Intelligence (AI) to support parts of our hiring process,including sourcing, screening, and evaluating candidates. AI helps assess applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.


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About Actalent

Sourced by ZipRecruiter

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

Industry

Business management consulting

Company size

5,001 - 10,000 Employees

Headquarters location

Hanover, MD, US

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