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Quality Engineer Manager Jobs in Riverside, CA (NOW HIRING)

Support management of cybersecurity-related nonconformances, CAPAs, deviations, and engineering changes through the quality management system, ensuring accurate documentation and timely follow-up. * ...

Senior Quality Engineer

Corona, CA · On-site

$91K - $123K/yr

Provide quality engineering leadership for new product introductions (NPI), manufacturing process ... Coordinate and facilitate risk management activities in accordance with ISO 14971, including hazard ...

Senior Quality Engineer

Corona, CA · On-site

$91K - $123K/yr

Provide quality engineering leadership for new product introductions (NPI), manufacturing process ... Coordinate and facilitate risk management activities in accordance with ISO 14971, including hazard ...

Senior Quality Engineer

Irvine, CA · On-site

$89 - $149/hr

Collaborate with suppliers to address quality concerns, manage supplier corrective actions ... Bachelors degree in a science, engineering or related discipline * Minimum of 2 years of quality ...

The Quality Engineer for our Maritime team is a critical role responsible for ensuring our ... Develop, implement, and sustain a robust Quality Management System (QMS) that is compliant with ...

Quality Engineer, Maritime

Santa Ana, CA · On-site

$74K - $96K/yr

The Quality Engineer for our Maritime team is a critical role responsible for ensuring our ... Develop, implement, and sustain a robust Quality Management System (QMS) that is compliant with ...

Quality Engineer III

Irvine, CA · On-site

$90 - $120/hr

This role plays a critical part in maintaining and improving our Quality Management System ... Partner with Engineering, Manufacturing, and Operations to support product development and ...

Quality Engineer III

Irvine, CA · On-site

$76K - $99K/yr

This role plays a critical part in maintaining and improving our Quality Management System ... Partner with Engineering, Manufacturing, and Operations to support product development and ...

Senior Quality Engineer

Irvine, CA · On-site

$89 - $149/hr

Collaborate with suppliers to address quality concerns, manage supplier corrective actions ... Bachelors degree in a science, engineering or related discipline * Minimum of 2 years of quality ...

Senior Quality Engineer

Irvine, CA · On-site

$89K - $148K/yr

Collaborate with suppliers to address quality concerns, manage supplier corrective actions ... Bachelors degree in a science, engineering or related discipline * Minimum of 2 years of quality ...

Senior Quality Engineer

Irvine, CA · On-site

$89K - $148K/yr

Collaborate with suppliers to address quality concerns, manage supplier corrective actions ... Bachelors degree in a science, engineering or related discipline * Minimum of 2 years of quality ...

... opening for a Supplier Quality Engineer responsible for managing supplier programs for ... Manage supplier related non-conforming material investigations, disposition, and manage supplier ...

... opening for a Supplier Quality Engineer responsible for managing supplier programs for ... Manage supplier related non-conforming material investigations, disposition, and manage supplier ...

Engineer, Quality MQA

Ontario, CA · On-site

$72K - $93K/yr

Job Purpose The Quality Engineer monitors field claim trends and inspects, evaluates, and tests ... Manage the master list for retrieved parts. Claims Improvement Activities - 30% * Identify and ...

Be Seen First

The Supplier Quality Engineer will be responsible for executing various supplier quality ... Project management, time management, problem solving and organization * Ability to work as an ...

Showing results 41-60

Quality Engineer Manager information

See Riverside, CA salary details

$62.6K

$116.5K

$165.4K

How much do quality engineer manager jobs pay per year?

As of Sep 2, 2026, the average yearly pay for quality engineer manager in Riverside, CA is $116,481.00, according to ZipRecruiter salary data. Most workers in this role earn between $96,000.00 and $136,700.00 per year, depending on experience, location, and employer.

What is a quality engineer manager?

Quality Engineer Managers are professionals responsible for overseeing the quality assurance processes within an organization. They lead teams of quality engineers to ensure products and services meet industry standards and customer expectations. Their duties typically include developing quality control policies, conducting audits, analyzing data, and working closely with other departments to implement improvements. By maintaining strict quality standards, they help minimize defects and ensure regulatory compliance. This role requires strong leadership, technical expertise, and effective communication skills.

How does a quality engineer manager typically collaborate with cross-functional teams to drive continuous improvement initiatives?

Quality Engineer Managers work closely with teams from production, engineering, supply chain, and customer service to identify process inefficiencies and quality concerns. They often facilitate root cause analyses, coordinate corrective actions, and lead regular meetings to monitor progress on quality objectives. By fostering open communication and shared accountability, they help ensure that all departments are aligned on quality standards and continuous improvement goals. This collaborative environment not only enhances product quality but also supports professional growth and innovation within the company.

What are the key skills and qualifications needed to thrive as a quality engineer manager, and why are they important?

To thrive as a Quality Engineer Manager, you need strong expertise in quality management systems, process improvement methodologies, and a relevant engineering degree or equivalent experience. Familiarity with tools like Six Sigma, ISO 9001 standards, and statistical analysis software is typically required, along with certifications such as CQE or Six Sigma Black Belt. Leadership, problem-solving, and effective communication are vital soft skills for driving teams and collaborating across departments. These competencies ensure product quality, regulatory compliance, and continuous operational improvement within the organization.

What is the difference between Quality Engineer Manager vs Quality Engineer?

AspectQuality Engineer ManagerQuality Engineer
ResponsibilitiesOversees quality teams, develops quality strategies, manages quality processesPerforms quality inspections, tests products, implements quality procedures
Required SkillsLeadership, project management, quality system knowledgeTechnical skills, attention to detail, testing expertise
CertificationsASQ CQE, Six Sigma Green/Black Belt often preferredASQ CQE, Six Sigma Green/Black Belt beneficial
Work EnvironmentManagement level, team coordination, strategic planningHands-on testing, process improvement, quality assurance

The main difference between a Quality Engineer Manager and a Quality Engineer lies in their scope of responsibilities. The manager oversees quality teams and strategic initiatives, while the engineer focuses on technical testing and process implementation. Both roles often require similar certifications like ASQ CQE and Six Sigma, but the manager's role emphasizes leadership and management skills.

What are the most commonly searched types of Quality Engineer jobs in Riverside, CA?

The most popular types of Quality Engineer jobs in Riverside, CA are:

What are popular job titles related to Quality Engineer Manager jobs in Riverside, CA?

For Quality Engineer Manager jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Quality Engineer Manager jobs in Riverside, CA look for?

The top searched job categories for Quality Engineer Manager jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Quality Engineer Manager jobs?

Cities near Riverside, CA with the most Quality Engineer Manager job openings:

Infographic showing various Quality Engineer Manager job openings in Riverside, CA as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $116,481 per year, or $56 per hour.

Cybersecurity Quality Engineer

Masimo

Irvine, CA • On-site

$85K - $105K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 3 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

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