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Biomedical Engineer Jobs in Riverside, CA (NOW HIRING)

Software Quality Engineer II

Irvine, CA · On-site

$75K - $100K/yr

Bachelor's degree in Computer Science, Software Engineering, Electrical Engineering, Biomedical Engineering, or related technical discipline. * Minimum 3 years of experience in Quality Engineering ...

S (Mechanical, Electrical, Biomedical Engineering, or equivalent) with industry experience. M.S. (Mechanical, Electrical, Biomedical Engineering, or equivalent) or higher education is a plus.

Software Quality Engineer II

Irvine, CA · On-site

$75K - $100K/yr

Bachelor's degree in Computer Science, Software Engineering, Electrical Engineering, Biomedical Engineering, or related technical discipline. * Minimum 3 years of experience in Quality Engineering ...

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Field Service Engineer performs on-site and shop technical service on a wide range of respiratory equipment devices including preventative maintenance, repairs and evaluations. Communicating with ...

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Field Service Engineer performs on-site and shop technical service on a wide range of respiratory equipment devices including preventative maintenance, repairs and evaluations. Communicating with ...

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Students graduating in 2026 or later with a Bachelor's degree in Computer Science, Software Engineering, Biomedical Engineering (with computational focus), or related field * Preference for students ...

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Biomedical Engineer information

See Riverside, CA salary details

$42.8K

$98.9K

$146.1K

How much do biomedical engineer jobs pay per year?

As of Jul 17, 2026, the average yearly pay for biomedical engineer in Riverside, CA is $98,909.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,700.00 and $121,000.00 per year, depending on experience, location, and employer.

What engineers make $500,000?

Highly experienced biomedical engineers working in senior roles, management, or specialized fields such as medical device development can earn salaries approaching or exceeding $500,000 annually, especially with bonuses and stock options. Achieving this level typically requires advanced degrees, extensive experience, and leadership responsibilities within the industry.

What jobs does biomedical engineering get you?

Biomedical engineering graduates can pursue careers as biomedical engineers, designing medical devices, equipment, and software. They may work in hospitals, research labs, or manufacturing companies, often requiring knowledge of biology, engineering principles, and regulatory standards.

What type of jobs do biomedical engineers do?

Biomedical engineers design and develop medical devices, equipment, and software used in healthcare, such as imaging systems, prosthetics, and diagnostic tools. They often work in research labs, hospitals, or manufacturing environments, applying engineering principles to improve patient care and medical technology. Strong knowledge of biology, engineering, and computer skills are essential for these roles.

What are biomedical engineers?

Biomedical engineers are professionals who apply principles of engineering and biological sciences to design, develop, and maintain equipment, devices, computer systems, and software used in healthcare. They work to improve the quality and effectiveness of patient care by creating technologies such as artificial organs, medical imaging devices, and prosthetics. Biomedical engineers often collaborate with doctors, researchers, and other engineers to solve clinical problems and advance medical technology. Their work can be found in hospitals, research facilities, manufacturing companies, and regulatory agencies.

What Do Biomedical Engineers Do?

A Biomedical Engineer is an expert in the fields of medicine and biological sciences. They use their extensive knowledge base to develop different kinds of equipment and devices with the end goal of improving the effectiveness of patient care. Biomedical Engineers are critical thinkers and analysts. Their time is spent brainstorming solutions to medical problems and designing new devices, such as diagnostic machinery and even equipment for artificial body part generation. It is the job of a Biomedical Engineer to maintain the equipment they develop and to train other clinicians on proper usage and upkeep. In addition to the hands-on aspect of this career, Biomedical Engineers also dedicate time to researching medical dilemmas, studying up on biological discoveries, and assisting in the development of new scientific advances.

What are some common challenges biomedical engineers face when working on interdisciplinary teams?

Biomedical engineers frequently collaborate with professionals from diverse backgrounds, including clinicians, software developers, and regulatory specialists. One common challenge is effectively communicating technical concepts to non-engineers and aligning project goals across disciplines. Navigating differing priorities and timelines can also require strong project management and interpersonal skills. Emphasizing clear communication and a willingness to learn from other fields helps biomedical engineers successfully contribute to innovative healthcare solutions.

What is the difference between Biomedical Engineer vs Mechanical Engineer?

AspectBiomedical EngineerMechanical Engineer
Required CredentialsBachelor's in Biomedical Engineering or related field; often licensed or certifiedBachelor's in Mechanical Engineering; licensure varies by role
Work EnvironmentHospitals, medical device companies, research labsManufacturing, automotive, aerospace, research facilities
Industry UsageHealthcare, medical device development, biotechAutomotive, aerospace, energy, manufacturing

Biomedical Engineers focus on designing and improving medical devices and healthcare solutions, working mainly in healthcare settings. Mechanical Engineers have a broader scope, working on machinery, systems, and products across various industries. While both roles require engineering degrees, their work environments and industry applications differ significantly.

What exactly do biomedical engineers do?

Biomedical engineers design, develop, and test medical devices, equipment, and software used in healthcare. They often work in laboratories or clinical settings, applying principles of engineering and biology to improve patient care and medical technology. Skills in electronics, materials science, and computer programming are commonly used in this field.

What are the key skills and qualifications needed to thrive as a Biomedical Engineer, and why are they important?

To thrive as a Biomedical Engineer, you need a solid background in biology, engineering principles, mathematics, and often at least a bachelor's degree in biomedical engineering or a related field. Familiarity with CAD software, medical imaging systems, and regulatory standards such as FDA guidelines is typically required. Strong problem-solving, communication, and teamwork skills help you collaborate with healthcare professionals and translate technical solutions into clinical practice. These competencies are crucial for developing safe, effective medical devices and technologies that improve patient outcomes.
What are the most commonly searched types of Biomedical Engineer jobs in Riverside, CA? The most popular types of Biomedical Engineer jobs in Riverside, CA are:
What are popular job titles related to Biomedical Engineer jobs in Riverside, CA? For Biomedical Engineer jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Biomedical Engineer jobs in Riverside, CA look for? The top searched job categories for Biomedical Engineer jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Biomedical Engineer jobs? Cities near Riverside, CA with the most Biomedical Engineer job openings:
Infographic showing various Biomedical Engineer job openings in Riverside, CA as of July 2026, with employment types broken down into 2% Internship, 80% Full Time, 2% Part Time, and 16% Contract. Highlights an 94% In-person, 2% Hybrid, and 4% Remote job distribution, with an average salary of $98,909 per year, or $47.6 per hour.
Software Quality Engineer II

Software Quality Engineer II

Masimo

Irvine, CA • On-site

$75K - $100K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 26 days ago


Job description


Job Summary
The Software Quality Engineer II supports the development and lifecycle management of software used in medical devices by ensuring quality, compliance, and effective risk management throughout the product lifecycle. This role partners closely with Software Engineering, Systems Engineering, Regulatory Affairs, and Product Development teams to provide quality oversight from concept through commercialization.
The Software Quality Engineer II is responsible for reviewing software design and development deliverables, supporting verification and validation activities, assessing software changes, and ensuring compliance with applicable domestic and international regulations and standards. This position also contributes to continuous improvement initiatives, complaint investigations, CAPA activities, and post-market quality processes.
Success in this role requires strong knowledge of software quality principles, medical device regulations, software development processes, and the ability to collaborate effectively in a fast-paced cross-functional environment.
Duties & Responsibilities
  • Partner with software development and cross-functional teams to ensure quality is integrated throughout the software development lifecycle.
  • Review and approve software development deliverables including requirements, architecture, risk documentation, test protocols, traceability, and validation records.
  • Support design control activities in compliance with applicable regulations and standards, including FDA 21 CFR Part 820, ISO 13485, IEC 62304, ISO 14971, and other applicable global requirements.
  • Participate in design reviews, phase gate reviews, and change control activities for software-based products and systems.
  • Review software verification and validation activities including unit, integration, system, cybersecurity, and user acceptance testing.
  • Support software risk management activities, including hazard analysis, failure mode assessments, and risk control verification.
  • Evaluate software defects, nonconformances, and quality events to determine product impact and required actions.
  • Participate in CAPA, complaint investigations, post-market surveillance, and field issue assessments involving software-related products.
  • Support internal audits, external audits, and regulatory inspections by preparing documentation and providing subject matter expertise.
  • Drive continuous improvement initiatives to strengthen software quality systems, processes, and compliance effectiveness.
  • Assist in the creation, review, and maintenance of Design History Files (DHF), Device Master Records (DMR), and quality records.
  • Mentor junior team members and provide guidance on software quality processes and best practices as needed.
  • Perform other duties or special projects as assigned.

Minimum & Preferred Qualifications and Experience
Minimum Qualifications
  • Bachelor's degree in Computer Science, Software Engineering, Electrical Engineering, Biomedical Engineering, or related technical discipline.
  • Minimum 3 years of experience in Quality Engineering, Quality Assurance, or Software Quality within a regulated industry.
  • Working knowledge of software development lifecycle (SDLC), Agile and/or waterfall development methodologies.
  • Experience supporting software verification and validation activities.
  • Knowledge of medical device regulations and standards such as FDA 21 CFR Part 820, ISO 13485, IEC 62304, and ISO 14971.
  • Experience with change control, nonconformance, CAPA, and complaint handling processes.
  • Strong analytical, problem-solving, and risk assessment skills.
  • Strong written and verbal communication skills with the ability to work cross-functionally.
  • Proficiency with Microsoft Office applications and quality documentation systems.

Preferred Qualifications
  • Experience supporting Software as a Medical Device (SaMD), embedded software, connected devices, or cybersecurity-focused products.
  • Experience with automated test tools, defect tracking systems, or application lifecycle management systems.
  • Certified Quality Engineer (CQE), Certified Software Quality Engineer (CSQE), or equivalent certification.
  • Experience in the medical device industry strongly preferred.
  • Master's degree in a related technical discipline.

Education
Bachelor's degree in Computer Science, Software Engineering, Electrical Engineering, Biomedical Engineering, or related technical discipline required; advanced degree preferred.
Compensation
The anticipated salary range for this position is $75,000 - $100,000 plus benefits. Actual placement within the range is dependent on multiple factors, including but not limited to skills, education, and experience. 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, schematics, and written instructions.
  • Ability to clearly document technical findings and communicate with cross-functional team members.

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 or walking through facilities.
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.

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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

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