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Internship Abbott Biomedical Engineering Jobs in Riverside, CA

Masimo

Cybersecurity Quality Engineer

Irvine, CA · On-site

$85K - $105K/yr

Bachelor's degree in Computer Engineering, Computer Science, Electrical Engineering, Biomedical ... internship, co-op, or project-based experience in regulated environments will be considered.

Masimo

Cybersecurity Quality Engineer

Irvine, CA

$85K - $105K/yr

Bachelor's degree in Computer Engineering, Computer Science, Electrical Engineering, Biomedical ... internship, co-op, or project-based experience in regulated environments will be considered.

PHS Bio-Medical Services

Area Manager

Chino, CA · On-site

$71K - $100K/yr

Leads the team of Account Managers, Account Coordinators, Biomedical Technicians and Biomed Support/Interns in the Biomedical engineering department for the allocated area. The individual is ...

Prime Healthcare

Area Manager

Chino, CA · On-site

$71K - $100K/yr

Leads the team of Account Managers, Account Coordinators, Biomedical Technicians and Biomed Support/Interns in the Biomedical engineering department for the allocated area. The individual is ...

PHS Bio-Medical Services

Area Manager

Chino, CA · On-site

Leads the team of Account Managers, Account Coordinators, Biomedical Technicians and Biomed Support/Interns in the Biomedical engineering department for the allocated area. The individual is ...

Bright Uro

RD Internship Medical Device Company

Irvine, CA · On-site

$18 - $23.25/hr

We are seeking several motivated interns to join our small, fast-moving team and contribute to ... Working toward a degree in Engineering (Electrical, Software, Mechanical, or Biomedical), Computer ...

Cordis

Quality Manufacturing Engineer

Irvine, CA · 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 ...

Cordis

Quality Manufacturing Engineer

Irvine, CA

$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 ...

PHS Bio-Medical Services

Business Analyst I

Ontario, CA

$66K - $95K/yr

Master's degree in business analytics, engineering, mathematics, computer science, or related field ... Pay Transparency BioMedical Services, Inc. offers competitive compensation and a comprehensive ...

PHS Bio-Medical Services

Business Analyst I

Ontario, CA · On-site

$70K - $99K/yr

Master's degree in business analytics, engineering, mathematics, computer science, or related field ... Pay Transparency BioMedical Services, Inc. offers competitive compensation and a comprehensive ...

Prime Healthcare

Business Analyst I

Ontario, CA · On-site

$70K - $99K/yr

Master's degree in business analytics, engineering, mathematics, computer science, or related field ... BioMedical Services, Inc. offers competitive compensation and a comprehensive benefits package that ...

All JobsAbbott Biomedical Engineering JobsInternship Abbott Biomedical Engineering JobsInternship Abbott Biomedical Engineering Jobs in Riverside, CA

Internship Abbott Biomedical Engineering information

See Riverside, CA salary details

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How much do internship abbott biomedical engineering jobs pay per hour?

As of Aug 28, 2026, the average hourly pay for internship abbott biomedical engineering 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 is an internship at Abbott in biomedical engineering?

An Internship at Abbott in Biomedical Engineering is a temporary position designed for students or recent graduates to gain hands-on experience in the biomedical engineering field within a leading healthcare company. Interns typically work on real-world projects related to medical devices, diagnostics, or research and development. The program offers mentorship, professional networking opportunities, and insight into Abbott's innovative technologies and workplace culture. It helps interns develop technical and soft skills valuable for future careers in biomedical engineering. Internships usually last for a few months and may lead to full-time opportunities after graduation.

What types of projects can an intern expect to work on during an Abbott biomedical engineering internship?

As an intern in Abbott's Biomedical Engineering program, you can expect to be involved in hands-on projects that support the development, testing, and improvement of medical devices and technologies. Typical responsibilities may include assisting in laboratory experiments, analyzing data, supporting design validation activities, or collaborating with cross-functional teams such as quality assurance and regulatory affairs. This experience not only helps you gain technical skills but also exposes you to the project lifecycle in a real-world healthcare setting, preparing you for future roles in the industry.

What are the key skills and qualifications needed to thrive as an intern in Abbott biomedical engineering, and why are they important?

To thrive as an Abbott Biomedical Engineering intern, you typically need a strong academic background in biomedical engineering or a related field, with coursework in biology, engineering principles, and mathematics. Familiarity with CAD software, laboratory instrumentation, and data analysis tools, as well as experience with regulatory standards, is highly valued. Strong problem-solving skills, effective teamwork, and clear communication help interns stand out in collaborative project environments. These skills and qualifications are important for contributing to innovative healthcare solutions while ensuring safety, compliance, and cross-functional collaboration.

What is the difference between Internship Abbott Biomedical Engineering vs Biomedical Engineering Intern?

AspectInternship Abbott Biomedical EngineeringBiomedical Engineering Intern
Required CredentialsEnrolled in or recent graduate of biomedical engineering or related fieldEnrolled in or recent graduate of biomedical engineering or related field
Work EnvironmentCorporate, manufacturing, and R&D settings within AbbottResearch labs, hospitals, or academic settings
Employer & Industry UsageAbbott, medical device and healthcare industryVarious companies, hospitals, academic institutions

Both roles typically require similar educational backgrounds and certifications. The main difference lies in the work environment: Abbott internships focus on corporate and industry-specific projects, while biomedical engineering internships may be in academic or research settings. The Abbott internship offers industry-specific experience within a leading healthcare company, whereas general biomedical engineering internships provide broader exposure to research and clinical environments.

What are popular job titles related to Internship Abbott Biomedical Engineering jobs in Riverside, CA?

For Internship Abbott Biomedical Engineering jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Internship Abbott Biomedical Engineering jobs in Riverside, CA look for?

The top searched job categories for Internship Abbott Biomedical Engineering jobs in Riverside, CA are:

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Internship Abbott Biomedical Engineering jobs near you
Infographic showing various Internship Abbott Biomedical Engineering job openings in Riverside, CA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $41,913 per year, or $20.2 per hour.

Cybersecurity Quality Engineer

Irvine, CA • On-site

Masimo
Medical Equipment and Supplies Manufacturing • 1 - 5K employees
Learn more about Masimoexternal

$85K - $105K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 28 days ago

Job description


Job Summary:
The Cybersecurity Quality Engineer supports the integration of cybersecurity requirements into the product development lifecycle and quality management system for Masimo medical device products. Working under the guidance of senior quality, software, and cybersecurity team members, this role assists in ensuring cybersecurity-related activities are documented, traceable, and executed in accordance with applicable regulatory requirements, quality system procedures, and internal standards. This is an early-career engineering role suited for an individual seeking to develop specialized experience at the intersection of quality systems, design controls, software quality, and medical device cybersecurity.
Duties & Responsibilities:
  • Support execution of cybersecurity quality activities across assigned product development programs, including documentation review, milestone tracking, and quality record maintenance.
  • Assist in the preparation, review, and maintenance of cybersecurity-related design control documentation, including threat modeling records, vulnerability assessments, security risk analyses, cybersecurity protocols, and test reports.
  • Maintain traceability between cybersecurity requirements, software design outputs, mitigation activities, and verification/validation records within the Design History File (DHF).
  • Support authoring, review, and periodic updates of cybersecurity-related quality system procedures, work instructions, templates, and documentation standards.
  • Assist in cybersecurity vulnerability monitoring and post-market surveillance activities, including tracking disclosed vulnerabilities, supporting impact assessments, and documenting remediation activities.
  • Support management of cybersecurity-related nonconformances, CAPAs, deviations, and engineering changes through the quality management system, ensuring accurate documentation and timely follow-up.
  • Participate in cross-functional design reviews, cybersecurity risk reviews, and project meetings, supporting quality representation for cybersecurity-related topics.
  • Collaborate with R&D, Software Engineering, Regulatory Affairs, Product Security, and Quality teams to support consistent application of cybersecurity quality requirements across development activities.
  • Support preparation of cybersecurity documentation required for audits, regulatory submissions, inspections, and internal quality reviews.
  • Assist in evaluation of third-party software components, open-source software dependencies, and Software Bill of Materials (SBOM) documentation to support cybersecurity traceability and risk awareness.
  • Support internal audits, readiness activities, and documentation reviews related to cybersecurity quality and design control compliance.
  • Stay current with evolving regulatory guidance, industry standards, and cybersecurity best practices relevant to medical device development.

Minimum & Preferred Qualifications and Experience:
Minimum Qualifications:
  • Bachelor's degree in Computer Engineering, Computer Science, Electrical Engineering, Biomedical Engineering, Software Engineering, or related technical discipline.
  • 0-3 years of experience in quality engineering, software quality, cybersecurity, product security, or related engineering field; relevant internship, co-op, or project-based experience in regulated environments will be considered.
  • Foundational understanding of cybersecurity concepts including vulnerability management, threat modeling, software security, network security, and secure development principles.
  • Familiarity with quality systems, design controls, software lifecycle documentation, or regulated engineering processes.
  • Strong attention to detail and ability to manage documentation accurately.
  • Effective written and verbal communication skills.
  • Ability to manage multiple tasks and priorities in a dynamic, cross-functional environment.

Preferred Qualifications:
  • Exposure to medical device, healthcare technology, embedded systems, or regulated software environments.
  • Familiarity with FDA 21 CFR Part 820, ISO 13485, ISO 14971, FDA cybersecurity guidance, or related regulatory expectations.
  • Awareness of standards such as AAMI TIR57, IEC 62304, IEC 81001-5-1, or NIST cybersecurity frameworks.
  • Exposure to Software Bill of Materials (SBOM), software traceability, or software quality documentation practices.
  • Foundational knowledge of software validation, software quality assurance, or secure SDLC practices.
  • Security+, ISC2 CC, or similar entry-level cybersecurity certification is a plus.

Education:
Bachelor's degree in Computer Engineering, Computer Science, Electrical Engineering, Biomedical Engineering, Software Engineering, or related technical discipline, or equivalent combination of education and experience.
Compensation: The anticipated salary range for this position is $85,000 -$105,000. Actual placement within the range is dependent on multiple factors, including but not limited to skills, experience and internal equity. This position also qualifies for up to 10% annual bonus based on Company, department, and individual performance.
  • Masimo offers benefits such as Medical, Dental, Vision, Life/AD&D, Disability Insurance, 401(k), Vacation, Sick, Holiday, Paid Maternity Leave, Flexible Spending Accounts, voluntary Accident, Critical Illness, Hospital, Long-Term Care, Employee Assistance Program, Pet Insurance, on-site Wellness Clinic, Fitness Center, Café. All benefits are subject to eligibility requirements.

Language requirements
  • Ability to read, write, and communicate effectively in English.
  • Ability to interpret technical documents, engineering data, schematics, and written procedures.
  • Ability to clearly document technical findings and effectively communicate across cross-functional teams.
Physical requirements/Work Environment
  • This position primarily works in an office environment and requires frequent sitting, standing, and walking. Daily use of a computer and other digital devices is required. This role may require standing for extended periods when facilitating meetings, supporting laboratory activities, or walking through facilities.
  • Must be able to move throughout office, laboratory, and light manufacturing environments as needed to support design reviews, product inspections, audits, and cross-functional collaboration.
  • Occasional lifting and carrying of materials or equipment up to 25 lbs. may be required.
  • Domestic and international travel up to 20-25% may be required to support supplier visits, audits, customer activities, or program-related meetings.
  • The physical demands of the position described herein are essential functions of the job and employees must be able to successfully perform these tasks for extended periods. Reasonable accommodations may be made for those individuals with real or perceived disabilities to perform the essential functions of the job described.

Masimo is proud to be an EEOE/, M/F/D/V, and we are committed to Diversity at the corporate level.
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About Masimo

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Irvine, CA, US

Year founded

1989

Social media

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