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Internship Medical Device Intern Jobs in Riverside, CA

Cordis

Quality Engineer I - Medical Device

Irvine, CA ยท On-site

$68K - $84K/yr

Bachelor's degree in mechanical engineering, Biomedical or Industrial Engineering, or other related engineering fields. * 2+ years in medical device production or previous internship or co-op ...

Danaher

Software Engineer Internships

Pomona, CA ยท On-site

By submitting your interest, you'll be among the first to know when internship opportunities open ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

BRIDGEMED SOLUTIONS INC

Entry Level Biologist

Irvine, CA ยท On-site

$20 - $23/hr

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

BRIDGEMED SOLUTIONS INC

Entry Level Biologist

Irvine, CA ยท On-site

$20 - $23/hr

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

BRIDGEMED SOLUTIONS INC

Entry Level Biologist

Irvine, CA ยท On-site

$20 - $23/hr

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

SpaceX

Fall 2026 Engineering Internship/Co-op

Irvine, CA ยท On-site

$30/hr

As an intern, you will work closely with your mentor and other employees who will help you apply ... medical coverage and a 401(k) retirement plan. Students joining SpaceX through our internship ...

Masimo

Cybersecurity Quality Engineer

Irvine, CA

$85K - $105K/yr

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

Masimo

Cybersecurity Quality Engineer

Irvine, CA ยท On-site

$85K - $105K/yr

... 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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Internship Medical Device Intern information

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How much do internship medical device intern jobs pay per hour?

As of Jul 25, 2026, the average hourly pay for internship medical device intern in Riverside, CA is $20.15, according to ZipRecruiter salary data. Most workers in this role earn between $16.78 and $21.83 per hour, depending on experience, location, and employer.

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 typically need a background in biomedical engineering, life sciences, or a related field, along with solid analytical and problem-solving skills. Familiarity with CAD software, laboratory equipment, and quality management systems, as well as knowledge of relevant regulatory standards, is often required. Strong teamwork, adaptability, and effective communication are essential soft skills for collaborating on cross-functional projects and presenting findings. These competencies ensure interns can contribute meaningfully to device development, comply with industry standards, and support innovation in a regulated environment.

What types of projects and responsibilities can I expect as a Medical Device Intern?

As a Medical Device Intern, you can expect to support ongoing projects in areas such as product development, testing, quality assurance, or regulatory affairs. Typical responsibilities may include assisting with laboratory experiments, documenting results, preparing technical reports, and collaborating with cross-functional teams like engineering, clinical, or manufacturing. Interns often gain exposure to the medical device lifecycle and learn about regulatory standards, making this role an excellent opportunity for hands-on learning and professional growth. You'll also have the chance to participate in team meetings and contribute ideas to improve product safety and effectiveness.

What does a Medical Device Intern do?

A Medical Device Intern typically assists in the development, testing, and documentation of medical devices under the supervision of experienced engineers or scientists. Their responsibilities may include conducting research, supporting design and prototyping, running laboratory tests, collecting and analyzing data, and ensuring compliance with regulatory standards. The internship provides hands-on experience and exposure to the medical device industry, helping students or recent graduates gain valuable skills and knowledge in the field.
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Internship Medical Device Intern jobs near you
Infographic showing various Internship Medical Device Intern job openings in Riverside, CA as of July 2026, with employment types broken down into 82% Full Time, 11% Part Time, and 7% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $41,913 per year, or $20.2 per hour.
Quality Engineer I - Medical Device

Quality Engineer I - Medical Device

Cordis

Irvine, CA โ€ข On-site

$68K - $84K/yr

Full-time

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

Job description

Overview
Selution, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease. Our mission is to revolutionize healthcare by creating next-generation solutions that address unmet and critical medical needs.
Responsibilities
The Quality Engineer I will be responsible for ensuring that our medical devices meet the highest quality standards throughout the process. The QE I will be responsible for supporting the team through production scale up and associated quality deliverables. The primary focus will be ensuring that our processes and products meet established quality standards through developing, implementing, and continuously improving quality management systems, ensuring compliance with regulations, standards, and customer requirements. The position will collaborate with cross-functional teams to help identify quality issues, drive process improvements, and champion a culture of quality excellence.
  • Quality Control: Monitor and implement quality control measures (including verification of materials, components, and finished products) at every stage of the process, ensuring compliance with regulatory standards and internal quality requirements.
  • Process Improvement: Continuously identify and implement process improvements to enhance product quality, reduce waste, and optimize efficiency.
  • Design control: Work closely with R&D engineers to ensure design control is followed.
  • Risk Assessment: Prepare risk assessment documentation related to processes and identify potential areas for risk mitigation to ensure the safety and efficacy of medical devices.
  • Regulatory Compliance: Stay up to date with regulatory requirements, standards, and guidelines relevant to the medical device industry and ensure that processes adhere to these regulations.
  • Root Cause Analysis: Participate in root cause analysis for quality issues and recommend / implement corrective actions.
  • Documentation: Assist in maintaining accurate and complete documentation of quality-related processes, inspections, and testing, ensuring compliance with company standards.
  • Data Analysis: Analyze process data and quality metrics to identify trends and areas for improvement.

Strategic Impact
  • Quality support to sustaining current process.
  • Quality leads to support and implementation of revised QS

Key Interactions
  • Report on Quality Engineering.
  • Potential to interact with all functions including suppliers and customers depending on the topic/project being led or supported.

Qualifications
Required Skills and Experience
  • Bachelor's degree in mechanical engineering, Biomedical or Industrial Engineering, or other related engineering fields.
  • 2+ years in medical device production or previous internship or co-op experience in quality assurance or is a plus.
  • Previous experience working in a clean room environment [preferred]
  • Strong engineering background
  • Strong analytical and problem-solving skills.
  • Strong communication skills.
  • Excellent attention to detail and organizational skills.
  • Ability to work collaboratively in a team environment.
  • Fluent in English

Physical Requirements
  • Light office work and telecommuting capability.
  • Available to travel 20% of the time, as required domestic and international.
  • Must be able to lift and carry up to 50 lbs.

Pay / Compensation
The expected pre-tax pay rate for this position is $68,200 - $84,700. Actual pay may fluctuate outside of the listed range depending on skills, education, experience, job-related knowledge and location.
US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa.
Preferred Qualifications
Cordis is proud to be an equal opportunity employer and is committed to providing equal opportunity for all teammates and applicants. At Cordis, our teammates all bring different strengths, experiences, and backgrounds, who share a passion for improving people's lives. Diversity not only includes race and gender identity, but also age, disability status, veteran status, sexual orientation, religion, and many other parts of one's identity. All our teammates' points of view are key to our success, and we believe inclusion is everyone's responsibility. Together, we strive to create and maintain working and learning environments that are inclusive, equitable and welcoming.

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