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Medical Device Internship Jobs in California (NOW HIRING)

Entry Level Biologist

Irvine, CA · On-site

$20 - $23/hr

... medical device, biotech, pharmaceutical, or regulated lab environment (internships welcome)  Strong attention to detail and organizational skills  Proficiency in Microsoft Excel, Word, and ...

Entry Level Biologist

Irvine, CA · On-site

$20 - $23/hr

... medical device, biotech, pharmaceutical, or regulated lab environment (internships welcome)  Strong attention to detail and organizational skills  Proficiency in Microsoft Excel, Word, and ...

Entry Level Biologist

Irvine, CA · On-site

$20 - $23/hr

... medical device, biotech, pharmaceutical, or regulated lab environment (internships welcome)  Strong attention to detail and organizational skills  Proficiency in Microsoft Excel, Word, and ...

Engineer II, R&D

Aliso Viejo, CA · On-site

$75K - $99K/yr

Knowledge of medical device and technical development. * Working knowledge of materials used in the medical device industry. * Experience from Engineering internship or rotation program preferred.

Engineer II, R&D

Aliso Viejo, CA · On-site

$75K - $99K/yr

Knowledge of medical device and technical development. * Working knowledge of materials used in the medical device industry. * Experience from Engineering internship or rotation program preferred.

Engineer II, R&D

Aliso Viejo, CA · On-site

$75K - $99K/yr

Knowledge of medical device and technical development. * Working knowledge of materials used in the medical device industry. * Experience from Engineering internship or rotation program preferred.

Engineer II, R&D

Aliso Viejo, CA · On-site

$75K - $99K/yr

Knowledge of medical device and technical development. * Working knowledge of materials used in the medical device industry. * Experience from Engineering internship or rotation program preferred.

Engineer II, R&D

Aliso Viejo, CA · On-site

$75K - $99K/yr

Knowledge of medical device and technical development. * Working knowledge of materials used in the medical device industry. * Experience from Engineering internship or rotation program preferred.

Engineer II, R&D

Aliso Viejo, CA · On-site

$80K - $94K/yr

Knowledge of medical device and technical development. * Working knowledge of materials used in the medical device industry. * Experience from Engineering internship or rotation program preferred.

Engineer II, R&D

Aliso Viejo, CA · On-site

$79K - $83K/yr

... medical device industry 7. Experience from Engineering internship or rotation program preferred 8. One (1) year of Manufacturing experience preferred EEO We are an equal employment opportunity ...

Engineer II, R&D

Aliso Viejo, CA · On-site

$80K - $94K/yr

Knowledge of medical device and technical development. * Working knowledge of materials used in the medical device industry. * Experience from Engineering internship or rotation program preferred.

Knowledge of medical device and technical development. * Working knowledge of materials used in the medical device industry. * Experience from Engineering internship or rotation program preferred.

Engineer II, R&D

Aliso Viejo, CA · On-site

$80K - $94K/yr

Knowledge of medical device and technical development. * Working knowledge of materials used in the medical device industry. * Experience from Engineering internship or rotation program preferred.

... internship, co-op, or project-based experience in regulated environments will be considered ... Exposure to medical device, healthcare technology, embedded systems, or regulated software ...

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Medical Device Internship information

See California salary details

$10

$19

$29

How much do medical device internship jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for medical device internship in California is $19.06, according to ZipRecruiter salary data. Most workers in this role earn between $15.91 and $20.62 per hour, depending on experience, location, and employer.

What is a medical device internship?

A Medical Device Internship is a short-term position, typically for students or recent graduates, that provides hands-on experience in the medical device industry. Interns may work in various areas such as research and development, quality assurance, regulatory affairs, or engineering. The goal is to give participants practical exposure to how medical devices are designed, manufactured, tested, and brought to market while working alongside professionals in the field. This experience can help interns build valuable skills, network with industry experts, and improve their chances of securing a full-time role after graduation.

What types of projects and responsibilities can I expect during a medical device internship?

As a Medical Device Intern, you will typically be involved in a variety of hands-on projects that support product development, testing, or regulatory compliance. Interns often assist with tasks such as prototyping, data analysis, documentation for regulatory submissions, and collaborating with engineers or quality assurance teams. You may also participate in cross-functional meetings, learn about industry standards, and contribute to process improvements. This experience provides valuable exposure to both technical and regulatory aspects of the medical device industry, helping you build a strong foundation for a future career.

What are the key skills and qualifications needed to thrive as a medical device intern, and why are they important?

To thrive as a Medical Device Intern, you need a background in biomedical engineering or a related field, strong analytical skills, and a basic understanding of medical device regulations. Familiarity with CAD software, laboratory equipment, and regulatory standards such as FDA or ISO is often required. Strong communication, teamwork, and problem-solving abilities help interns contribute effectively to multidisciplinary projects. These skills ensure that interns can support innovation, comply with industry standards, and work efficiently within development teams.

What is the difference between Medical Device Internship vs Medical Device Technician?

AspectMedical Device InternshipMedical Device Technician
Required CredentialsTypically pursuing or recent graduate in biomedical, mechanical, or related fieldsPost-secondary certification or associate degree in biomedical technology or related field
Work EnvironmentOffice, laboratory, or manufacturing settings; focus on learning and trainingClinical, hospital, or repair facilities; hands-on device maintenance and troubleshooting
Employer & Industry UsageMedical device companies, hospitals, research institutions; internship programsMedical device manufacturing, healthcare facilities, repair services
Common Search & Comparison IntentEntry-level learning experience, career explorationTechnical repair, device maintenance, troubleshooting skills

The main difference between a Medical Device Internship and a Medical Device Technician is that internships are training roles for students or recent graduates focusing on learning about medical devices, while technicians are trained professionals responsible for maintaining, repairing, and troubleshooting medical devices in clinical or manufacturing settings.

What are the most commonly searched types of Medical Device jobs in California?

The most popular types of Medical Device jobs in California are:

What cities in California are hiring for Medical Device Internship jobs?

Cities in California with the most Medical Device Internship job openings:

Infographic showing various Medical Device Internship 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 $39,648 per year, or $19.1 per hour.

Complaint Evaluation Engineer

Applied Medical

Rancho Santa Margarita, CA • On-site

$72K/yr

Full-time

Medical, Life, Retirement, PTO

Re-posted 10 days ago


Applied Medical rating

8.0

Company rating: 8.0 out of 10

Based on 23 frontline employees who took The Breakroom Quiz


Job description

Applied Medical is a new-generation medical device company with a proven business model and commitment to innovation fueled by rapid business growth and expansion. Our company has been developing and manufacturing advanced surgical technologies for over 35 years and has earned a strong reputation for excellence in the healthcare field. Our unique business model, combined with our dedication to delivering the highest quality products, enables team members to contribute to a larger capacity than is possible in typical positions.
Position Description
Position Overview: The Complaint Evaluation Engineer plays a critical role in Applied Medical's post-market quality and patient safety efforts by investigating returned medical devices and evaluating real-world product performance. This hands-on, laboratory-based engineering role focuses on device teardown, functional and mechanical testing, and recreation of reported product issues to determine root cause and support continuous improvement. Working closely with cross-functional engineering and quality teams, the complaint evaluation engineer contributes to regulatory compliance, technical documentation, and post-market surveillance activities in alignment with Food and Drug Administration standards, International Organization for Standardization (ISO) 13485 requirements, and Medical Device Reporting expectations. This position is well-suited for engineering professionals seeking experience in medical device investigation, failure analysis, and post-market quality engineering.
Key Responsibilities
  • Perform complaint evaluations and investigations by conducting visual, mechanical, and functional assessments of returned medical devices to evaluate real-world product performance.
  • Execute root cause analysis activities by disassembling devices, recreating reported issues, and applying structured problem-solving methodologies to identify underlying causes.
  • Conduct hands-on laboratory testing and troubleshooting using test fixtures, measurement tools, and simulated clinical-use conditions to validate investigative findings.
  • Prepare technical documentation and reports that clearly summarize test methods, results, conclusions, and recommendations in accordance with FDA, ISO 13485, and Medical Device Reporting requirements.
  • Collaborate cross-functionally with research and development, manufacturing, quality, and clinical development teams to communicate findings and support post-market regulatory activities.
  • Support continuous improvement initiatives by contributing to enhancements in test methods, investigative processes, and documentation practices.
  • Participate in training and professional development to apply feedback constructively and strengthen technical and analytical capabilities.
  • Success in This Role Looks Like
  • Delivering accurate and thorough investigations that identify root cause and support patient safety and product quality.
  • Producing clear, compliant technical reports that meet post-market regulatory and quality system expectations.
  • Effectively collaborating with cross-functional engineering teams to communicate findings and escalate product concerns.
  • Consistently applying structured problem-solving approaches to complex medical device performance issues.
  • Contributing to process improvements that enhance complaint evaluation efficiency, consistency, and technical rigor.

Success in This Role Looks Like:
  • Delivering accurate and thorough investigations that identify root cause and support patient safety and product quality.
  • Producing clear, compliant technical reports that meet post-market regulatory and quality system expectations.
  • Effectively collaborating with cross-functional engineering teams to communicate findings and escalate product concerns.
  • Consistently applying structured problem-solving approaches to complex medical device performance issues.
  • Contributing to process improvements that enhance complaint evaluation efficiency, consistency, and technical rigor.

Position Requirements
The following skills and attributes are required:
  • Work onsite in a highly collaborative engineering and laboratory environment
  • Bachelor's degree in Mechanical Engineering, Biomedical Engineering, Electrical Engineering, or a related field
  • Minimum of one year of experience in a regulated industry, such as medical device, pharmaceutical, laboratory, aerospace, or strong internship and lab experience
  • Demonstrate strong problem-solving abilities, critical thinking, and a root-cause-focused mindset
  • Ability to take and apply feedback constructively
  • Effective written and verbal communication skills
  • Proficient with spreadsheets, word processing, and technical documentation tools
  • Strong organizational skills and the ability to manage multiple investigations simultaneously
  • Comfortable performing hands-on testing, troubleshooting, and mechanical/electrical evaluation of devices
  • Comfortable handling, inspecting, and testing returned medical devices that have been used in clinical and surgical environments, in accordance with safety and biohazard handling procedures

Preferred
The following skills and attributes are preferred:
  • Experience with failure analysis, complaint investigations, or reliability testing in a regulated environment.
  • Familiarity with post-market regulatory systems, including Medical Device Reporting, corrective and preventive action processes, and quality management system requirements.
  • Understanding of laboratory testing protocols and test equipment used in mechanical or electrical evaluation.
  • Comfortable handling, inspecting, and testing returned medical devices that have been used in clinical and surgical environments, in accordance with safety and biohazard handling procedures.
  • Experience working in an FDA-regulated or ISO 13485-certified organization.
  • Technical writing experience, including preparation of engineering reports or regulatory documentation.
  • Strong analytical capability with an ability to understand integrated mechanical and electrical systems.

Benefits
  • Competitive compensation range: $71000 - $80000 / year (California).
  • Comprehensive benefits package.
  • Training and mentorship opportunities.
  • On-campus wellness activities.
  • Education reimbursement program.
  • 401(k) program with discretionary employer match.
  • Generous vacation accrual and paid holiday schedule.

Please note that the compensation range may be adjusted in the future, and bonus and incentive compensation plans may apply.
Our total reward package reflects our commitment to employee growth and well-being, as we invest in your development and offer a range of benefits designed to enhance your career and life.
All compensation and benefits are subject to plan documents and written agreements.
Equal Opportunity Employer
Applied Medical is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, disability (mental and physical), exercising the right to family care and medical leave, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, political affiliation, race, religious creed, sex (including pregnancy, childbirth, breastfeeding and related medical conditions), or sexual orientation, or any other status protected by federal, state or local laws in the locations where Applied Medical operates.

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