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Embedded Software Verification Engineer Jobs in Riverside, CA

Masimo

Software Quality Engineer II

Irvine, CA · On-site

... Review software verification and validation activities including unit, integration, system ... Preferred : • Experience supporting Software as a Medical Device (SaMD), embedded software ...

Masimo

Software Quality Engineer II

Irvine, CA · On-site

$75K - $100K/yr

Review software verification and validation activities including unit, integration, system ... Experience supporting Software as a Medical Device (SaMD), embedded software, connected devices, or ...

Masimo

Software Quality Engineer II

Irvine, CA · On-site

$75K - $100K/yr

Review software verification and validation activities including unit, integration, system ... Experience supporting Software as a Medical Device (SaMD), embedded software, connected devices, or ...

Neon Aerospace

Senior Embedded Platform Engineer

Irvine, CA

$133K - $174K/yr

We're seeking a Senior Platform/Real-Time Embedded Firmware Engineer with strong low-level embedded ... software development processes. * Contribute to requirements, traceability, verification planning ...

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All JobsEmbedded Software Verification Engineer JobsEmbedded Software Verification Engineer Jobs in Riverside, CA

Embedded Software Verification Engineer information

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$73K

$160K

$181.5K

How much do embedded software verification engineer jobs pay per year?

As of Aug 22, 2026, the average yearly pay for embedded software verification engineer in Riverside, CA is $160,020.00, according to ZipRecruiter salary data. Most workers in this role earn between $137,200.00 and $180,500.00 per year, depending on experience, location, and employer.

What does an embedded software verification engineer do?

An Embedded Software Verification Engineer is responsible for ensuring that embedded software systems function correctly and meet design requirements. They create and execute tests, analyze results, and identify software defects in embedded systems such as automotive controllers, medical devices, or consumer electronics. This role typically involves working closely with software developers and hardware engineers to review code, develop test plans, and use debugging tools to validate the software’s functionality, performance, and safety. Their work is crucial for delivering reliable products that operate safely and efficiently in real-world environments.

What are the key skills and qualifications needed to thrive as an embedded software verification engineer?

To thrive as an Embedded Software Verification Engineer, a strong background in embedded systems, programming (C/C++), and software testing methodologies is essential, typically supported by a degree in computer science, electrical engineering, or a related field. Familiarity with tools such as MATLAB/Simulink, debuggers, oscilloscopes, and verification frameworks, as well as certifications like ISTQB, are commonly required. Attention to detail, problem-solving abilities, and effective communication help engineers identify issues and work collaboratively in cross-functional teams. These skills ensure the development of reliable, safe, and high-quality embedded systems in safety-critical industries.

What are some common challenges faced by embedded software verification engineers during the validation process?

Embedded Software Verification Engineers often encounter challenges such as limited hardware availability, rapidly changing requirements, and integration issues with multiple hardware and software components. Debugging in an embedded environment can be more complex due to constrained system resources and limited visibility into the hardware-software interactions. Collaborating closely with both hardware and firmware teams is essential to quickly identify and resolve defects, making strong communication and problem-solving skills crucial for success in this role.

What is the difference between Embedded Software Verification Engineer vs Embedded Software Developer?

AspectEmbedded Software Verification EngineerEmbedded Software Developer
Primary FocusVerifying and validating embedded software to ensure quality and reliabilityDesigning, coding, and implementing embedded software solutions
Skills & CertificationsKnowledge of testing tools, verification processes, embedded systems, certifications like ISTQBProficiency in programming languages (C, C++), embedded systems, software development certifications
Work EnvironmentTesting labs, development teams, quality assurance departmentsDevelopment teams, R&D labs, product engineering

While both roles require embedded systems knowledge and programming skills, the Embedded Software Verification Engineer primarily focuses on testing, validation, and ensuring software quality, whereas the Embedded Software Developer concentrates on creating and implementing embedded software solutions.

What are popular job titles related to Embedded Software Verification Engineer jobs in Riverside, CA?

For Embedded Software Verification Engineer jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Embedded Software Verification Engineer jobs in Riverside, CA look for?

The top searched job categories for Embedded Software Verification Engineer jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Embedded Software Verification Engineer jobs?

Cities near Riverside, CA with the most Embedded Software Verification Engineer job openings:

Embedded Software Verification Engineer jobs near you

Software Quality Engineer II

Masimo

Irvine, CA • On-site

Full-time

Re-posted yesterday

Job description

Job Summary:
Masimo is a company focused on the development and lifecycle management of software for medical devices. The Software Quality Engineer II role involves ensuring quality and compliance throughout the product lifecycle while collaborating with various engineering and regulatory teams.
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.
Qualifications:
Required:
• 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.
• 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.
Preferred:
• 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.
Company:
Masimo is a medical technology company that develops and manufactures noninvasive patient monitoring devices for healthcare settings. It is a sub-organization of Danaher. Founded in 1989, the company is headquartered in Irvine, USA, with a team of 1001-5000 employees. The company is currently Late Stage.
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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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