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Design Quality Engineer Jobs in California (NOW HIRING)

Masimo

Sr Quality Engineer, NPD/NPI

Irvine, CA · On-site

$105K - $135K/yr

The Sr. Quality Engineer, NPD/NPI is responsible for ensuring design quality and regulatory compliance throughout the new product development lifecycle for Masimo products. This position provides ...

Wisk

Quality Engineer

Hollister, CA · On-site

$92K - $113K/yr

Proven ability to interpret and critique design drawings, process specifications, and autoclave ... ASQ Certified Quality Engineer (CQE), Six Sigma Green belt or equivalent. * Experience using the ...

Masimo

Sr Quality Engineer, NPD/NPI

Irvine, CA · On-site

$105K - $135K/yr

The Sr. Quality Engineer, NPD/NPI is responsible for ensuring design quality and regulatory compliance throughout the new product development lifecycle for Masimo products. This position provides ...

Wisk Aero

Quality Engineer

Hollister, CA · On-site

$92K - $113K/yr

Proven ability to interpret and critique design drawings, process specifications, and autoclave ... ASQ Certified Quality Engineer (CQE), Six Sigma Green belt or equivalent. * Experience using the ...

Pivotal

Quality Engineer

Palo Alto, CA · On-site

$101K - $125K/yr

We design, develop, and manufacture light eVTOL aircraft and are renowned for the BlackFly aircraft ... We are seeking a Quality Engineer with a strong background in composites manufacturing and ...

Pivotal

Quality Engineer

Palo Alto, CA · On-site

$101K - $125K/yr

We design, develop, and manufacture light eVTOL aircraft and are renowned for the BlackFly aircraft ... We are seeking a Quality Engineer with a strong background in composites manufacturing and ...

Pivotal

Quality Engineer

Palo Alto, CA · On-site

$101K - $125K/yr

We design, develop, and manufacture light eVTOL aircraft and are renowned for the BlackFly aircraft ... We are seeking a Quality Engineer with a strong background in composites manufacturing and ...

Heartflow

Staff Device Quality Engineer

San Francisco, CA · On-site

$84K - $109K/yr

As a Staff Device Quality Engineer, you will serve as the senior technical authority for software quality and design excellence across multiple product lines and platform initiatives. In this highly ...

Space Kinetic

Quality Engineer

El Segundo, CA · On-site

$76K - $99K/yr

This role serves as a technical partner throughout the product lifecycle, helping engineers design quality into our products rather than inspecting it in after the fact. This role will support the ...

CYNET SYSTEMS

Quality Engineer

Irvine, CA · On-site

$35 - $40/hr

Experience with MS Office Suite and statistical analysis tool, CAD experience preferred ... engineering staff to determine quality and reliability standards. Skills: * Verbal and written ...

Singer Vehicle Design

Supplier Quality Engineer

Carson, CA · On-site

$72K - $156K/yr

Join Our Relentless Pursuit of Excellence At Singer Vehicle Design, we believe Everything is ... The Supplier Quality Engineer shall use their experience and knowledge to help determine the best ...

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All JobsDesign Quality Engineer JobsDesign Quality Engineer Jobs in California

Design Quality Engineer information

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$18

$46

$69

How much do design quality engineer jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for design quality engineer in California is $46.57, according to ZipRecruiter salary data. Most workers in this role earn between $38.17 and $55.77 per hour, depending on experience, location, and employer.

How does a design quality engineer typically collaborate with cross-functional teams during product development?

As a Design Quality Engineer, you work closely with teams such as R&D, manufacturing, regulatory affairs, and supply chain throughout the product development lifecycle. Your primary role is to ensure quality standards are integrated from the initial concept through to product launch. This often involves participating in design reviews, facilitating risk assessments like FMEA, and ensuring compliance with relevant regulations. Effective communication and problem-solving skills are essential, as you'll help bridge gaps between design intent and manufacturability to ensure a smooth transition to production.

What are the key skills and qualifications needed to thrive as a design quality engineer?

To thrive as a Design Quality Engineer, you need a solid background in engineering principles, quality assurance methodologies, and a relevant degree such as mechanical or electrical engineering. Familiarity with standards like ISO 13485 or ISO 9001, proficiency in tools such as FMEA, risk analysis software, and statistical analysis platforms like Minitab are typically required. Strong problem-solving abilities, attention to detail, and effective communication skills help distinguish top performers in this role. These skills ensure that products meet regulatory requirements, maintain high quality standards, and minimize risk throughout the design and development process.

What is a design quality engineer?

Design Quality Engineers are professionals who ensure that products are developed and manufactured according to quality standards and regulatory requirements. They work closely with design, engineering, and manufacturing teams to identify potential risks, implement quality controls, and validate product designs. Their goal is to make sure that products are safe, effective, and meet customer expectations before they are released to the market.

What is the difference between Design Quality Engineer vs Manufacturing Quality Engineer?

AspectDesign Quality EngineerManufacturing Quality Engineer
Primary FocusEnsuring product design meets quality standards and specifications during developmentMonitoring and improving quality in manufacturing processes and final products
Work EnvironmentDesign labs, R&D departments, product development teamsProduction lines, manufacturing plants, quality control departments
Required CredentialsBachelor's in Engineering, Quality certifications (e.g., CQE), knowledge of design standardsBachelor's in Engineering or Manufacturing, Quality certifications, process improvement skills

Design Quality Engineers focus on product design and development to prevent defects early, while Manufacturing Quality Engineers concentrate on maintaining quality during production. Both roles require similar credentials and work within quality assurance but target different stages of the product lifecycle.

Are design quality engineers well paid?

Design quality engineers typically earn competitive salaries that reflect their technical expertise in quality assurance, design review, and engineering standards. Salaries vary based on experience, industry, and location, but they are generally above average compared to other engineering roles. Certifications like Six Sigma or ISO standards can also influence compensation levels.
What are the most commonly searched types of Design Quality Engineer jobs in California? The most popular types of Design Quality Engineer jobs in California are:
What are popular job titles related to Design Quality Engineer jobs in California? For Design Quality Engineer jobs in California, the most frequently searched job titles are:
What job categories do people searching Design Quality Engineer jobs in California look for? The top searched job categories for Design Quality Engineer jobs in California are:
What cities in California are hiring for Design Quality Engineer jobs? Cities in California with the most Design Quality Engineer job openings:
What are popular job titles related to Design Quality Engineer jobs in CA? For Design Quality Engineer jobs in CA, the most frequently searched job titles are:
Design Quality Engineer jobs near you
Infographic showing various Design Quality Engineer job openings in California as of July 2026, with employment types broken down into 88% Full Time, 10% Part Time, and 2% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $96,860 per year, or $46.6 per hour.

Sr Quality Engineer, NPD/NPI

Masimo

Irvine, CA • On-site

$105K - $135K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 16 days ago

Job description


Job Summary:
The Sr. Quality Engineer, NPD/NPI is responsible for ensuring design quality and regulatory compliance throughout the new product development lifecycle for Masimo products. This position provides quality engineering support across cross-functional development teams through design control documentation, process execution, and risk management activities, while coordinating with Sustaining Quality and Regulatory Affairs as required to ensure successful and compliant product launches.
Duties & Responsibilities:
  • Lead quality engineering activities across assigned new product development programs, ensuring compliance with applicable regulatory requirements, quality system procedures, and industry standards throughout the product lifecycle
  • Author, review, and approve quality documentation including design control records, risk management files, test protocols, test reports, and product specifications in support of program milestones and design reviews
  • Serve as the quality representative on cross-functional project teams, providing guidance on design control requirements, regulatory strategy, and quality risk considerations from concept through commercial release
  • Identify, escalate, and drive resolution of quality and compliance issues encountered during product development, applying structured problem-solving methodologies to determine root cause and implement effective corrective actions
  • Plan and support design verification and validation activities, including protocol development, execution oversight, and results review, to ensure products meet defined user needs and intended use requirements
  • Support internal and external audits by preparing documentation, responding to findings, and leading corrective action efforts within areas of responsibility
  • Initiate, track, and manage nonconformances, CAPAs, and engineering changes through the quality management system, ensuring timely closure and effectiveness verification
  • Maintain and improve quality system procedures and work instructions within areas of assigned responsibility, ensuring alignment with current regulatory requirements and best practices
  • Mentor junior quality engineers on design control processes, documentation standards, and quality system requirements, supporting team capability development
  • Collaborate with Regulatory Affairs, R&D, Operations, and Supply Chain to ensure quality requirements are effectively integrated into product and process design decisions
  • Monitor and communicate product and program quality metrics, proactively identifying trends and recommending corrective or preventive actions as appropriate
  • Support post-market quality activities, including complaint investigations, field corrective actions, and design changes, ensuring continuity between development and sustaining quality functions

Minimum & Preferred Qualifications and Experience:
Minimum Qualifications:
  • Bachelor's degree in Engineering, Life Sciences, or related technical discipline, or equivalent combination of education and experience required.
  • Minimum 6-8+ years of quality engineering experience within a regulated medical device or similarly regulated environment.
  • Strong knowledge of FDA 21 CFR Part 820, ISO 13485, ISO 14971, and quality system principles.
  • Demonstrated experience supporting new product development, design transfer, validation, and commercialization activities.
  • Proven experience authoring and managing design control documentation including DHF records, risk files, protocols, reports, and engineering documentation.
  • Experience with quality management systems (QMS), including CAPA, nonconformance management, change control, and document control processes.
  • Strong analytical, problem-solving, and root cause investigation skills.
  • Ability to manage multiple priorities independently in a fast-paced, cross-functional development environment.
  • Strong written and verbal communication skills, with the ability to effectively communicate technical and compliance information across all levels of the organization.

Preferred Qualifications:
  • Experience supporting Class II and/or Class III medical device development.
  • Experience with design transfer, manufacturing readiness, and NPI implementation activities.
  • Familiarity with FDA submission pathways, including 510(k), PMA, or De Novo.
  • Experience supporting FDA inspections, ISO audits, supplier audits, or Notified Body interactions.
  • Familiarity with IEC 60601, IEC 62366, ISO 80601 series, or other applicable product-specific standards.
  • ASQ Certified Quality Engineer (CQE) or equivalent professional certification preferred.
  • Familiarity with Agile, phase-gate, or structured product development methodologies within a regulated environment.

Education:
Bachelor's degree in Engineering, Life Sciences, or related technical discipline, or equivalent work experience.
Compensation
The anticipated salary range for this position is $105,000 - $135,000 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, 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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