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Medical Device Development Jobs in California (NOW HIRING)

Medical Device Engineer Support the development, validation, and optimization of electrochemical test methods used for next-generation medical monitoring technologies. Partner with engineers to ...

Pay Rate Low: 22 | Pay Rate High: 25 Medical Device Assembler Santa Rosa, CA | 4/10 Schedule | $22 ... Strong training program with significant investment in employee development * Access to employee ...

Johnson & Johnson is rapidly expanding and is immediately hiring qualified Medical Device Assemblers to support production demand and new product development. Position Summary: As a Medical Device ...

Johnson & Johnson is rapidly expanding and is immediately hiring qualified Medical Device Assemblers to support production demand and new product development. Position Summary: As a Medical Device ...

Medical Device Rep

Santa Barbara, CA · On-site

$82K - $113K/yr

We are a fully integrated company with internal resources dedicated to the development and promotion of medical supplies and device products. We believe that our proven products and customer focused ...

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Showing results 1-20

Medical Device Development information

See California salary details

$28.6K

$52.7K

$79.9K

How much do medical device development jobs pay per year?

As of Jul 15, 2026, the average yearly pay for medical device development in California is $52,718.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,900.00 and $59,200.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in Medical Device Development, and why are they important?

To thrive in Medical Device Development, you need expertise in engineering or life sciences, a solid understanding of regulatory requirements, and often an advanced degree such as a master's or Ph.D. in a relevant field. Familiarity with CAD software, prototyping tools, and knowledge of FDA or ISO regulatory standards is typically required. Strong problem-solving abilities, collaboration, and effective communication distinguish top professionals in this field. These skills ensure the development of safe, innovative, and compliant medical devices that meet both user needs and regulatory standards.

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

AspectMedical Device DevelopmentMedical Device Quality Assurance
CredentialsEngineering degrees, certifications like RAPS or regulatory trainingQuality certifications, ISO 13485, regulatory compliance training
Work EnvironmentDesign labs, R&D teams, product development settingsManufacturing sites, quality control labs, compliance departments
Industry UsageDesigning and creating new medical devicesEnsuring devices meet quality and regulatory standards

Medical Device Development focuses on designing and creating new medical devices, involving engineering and product innovation. Medical Device Quality Assurance ensures these devices meet safety, quality, and regulatory standards through testing and compliance processes. Both roles are essential in the medical device industry but serve different functions in the product lifecycle.

What are some common challenges faced by professionals in medical device development, and how can they be addressed?

Professionals in medical device development frequently encounter challenges such as navigating complex regulatory requirements, ensuring product safety and efficacy, and managing cross-functional collaboration between engineering, clinical, and regulatory teams. Addressing these challenges requires staying updated on evolving regulations, fostering open communication among diverse team members, and implementing robust quality control processes. Proactively engaging with regulatory bodies and regularly reviewing project milestones can help streamline development and reduce the risk of costly delays.

What is medical device development?

Medical device development is the process of designing, creating, testing, and bringing medical devices to market. This process involves multiple stages, including concept development, prototyping, preclinical and clinical testing, regulatory approval, and manufacturing. The goal is to ensure that new devices are safe, effective, and meet regulatory standards before they are used by healthcare professionals or patients. Teams in medical device development often include engineers, scientists, regulatory specialists, and quality assurance professionals.
What are popular job titles related to Medical Device Development jobs in California? For Medical Device Development jobs in California, the most frequently searched job titles are:
What cities in California are hiring for Medical Device Development jobs? Cities in California with the most Medical Device Development job openings:
Infographic showing various Medical Device Development job openings in California as of July 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, 1% Temporary, and 2% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $52,718 per year, or $25.3 per hour.
Medical Device Engineer

Medical Device Engineer

Actalent

San Diego, CA

$50/hr

Contractor

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 days ago


Job description

Job Title: Medical Device Engineer

Job Description

Support the development, validation, and optimization of electrochemical test methods used for next-generation medical monitoring technologies. Partner with engineers to execute validation activities, perform laboratory testing, analyze data, and generate technical documentation supporting test method development and equipment qualification efforts.

Responsibilities

  • Draft validation protocols and reports.
  • Conduct test method validations.
  • Support equipment qualification activities.
  • Troubleshoot laboratory systems.
  • Execute test scripts.
  • Maintain calibration and qualification records.
  • Analyze experimental data.
  • Support engineering change control processes.

Essential Skills

  • Experience in test method validation and testing.
  • R&D experience executing test methods and supporting validation activities.
  • Skill in drafting validation protocols, reports, work instructions, and technical documentation.
  • Ability to analyze experimental data and draw statistically supported conclusions.
  • Experience in a regulated laboratory, medical device, biotech, or engineering environment.
  • Strong communication skills for collaboration across engineering teams.
  • Knowledge of electrochemistry, IQ, OQ, GMP, change controls, JMP, SolidWorks, and equipment qualification.

Additional Skills & Qualifications

  • Bachelor's degree in Engineering, Biomedical Engineering, Chemical Engineering, Mechanical Engineering, Materials Engineering, or a related technical discipline preferred.
  • Minimum 2 years of experience in laboratory testing, validation, engineering support, or medical device development.
  • Experience executing and documenting test method validations.
  • Technical writing experience supporting engineering or quality documentation.
  • Ability to perform statistical analysis and interpret engineering test data.
  • Experience with MSA/Gage R&R studies preferred.
  • Experience supporting IQ/OQ activities preferred.
  • Familiarity with equipment qualification, calibration, and validation documentation.
  • Medical device industry experience preferred.
  • Experience with electrochemical test systems is highly desirable.
  • Proficiency with Excel required; JMP and SolidWorks preferred.

Work Environment

R&D environment supporting product development and test method validation. Cross-functional collaboration with engineers, scientists, and technicians. Mix of laboratory testing, data analysis, technical writing, and validation activities. Standard business hours with hands-on laboratory work in a highly regulated medical device development setting.

Job Type & Location

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

Pay and Benefits

The pay range for this position is $50.00 - $50.00/hr.

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 Jul 24, 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 without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment 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 the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall 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 applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.


Actalent logo

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.

Company size

5,001 - 10,000 Employees

Headquarters location

Hanover, MD, US

Year founded

1983

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