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Quality Systems Engineer Jobs in California (NOW HIRING)

MicroVention

Sr. Engineer, Quality Systems

Aliso Viejo, CA · On-site

$100K - $125K/yr

This is a hands-on position in which the Senior Quality Systems Engineer is an active contributor to maintaining and improving quality systems to ensure compliance with global regulatory requirements ...

Teradyne

Senior Systems Quality Engineer

Sunnyvale, CA · On-site

$162 - $259/hr

Senior Systems Quality Engineer (Integrated System Test, Sunnyvale) Date: Aug 11, 2026 Location: Sunnyvale, CA, US We are the global test and automation specialists, powering next-generation ...

BALT Group

Quality System Engineer II

Irvine, CA · On-site

This Quality Engineer will be expected to work directly with different functions while receiving ... Job Responsibilities Knowledge of quality systems for medical device manufacturing and requirements ...

BALT Group

Quality System Engineer II

Irvine, CA · On-site

This Quality Engineer will be expected to work directly with different functions while receiving ... Job Responsibilities Knowledge of quality systems for medical device manufacturing and requirements ...

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How much do quality systems engineer jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for quality systems engineer in California is $49.37, according to ZipRecruiter salary data. Most workers in this role earn between $37.98 and $53.37 per hour, depending on experience, location, and employer.

What is a quality systems engineer?

Quality Systems Engineers are professionals responsible for designing, implementing, and maintaining quality management systems within an organization. They ensure that products or services meet established standards and regulatory requirements by developing processes, conducting audits, and analyzing data to identify areas for improvement. Their role often involves collaborating with other departments, training staff on quality procedures, and ensuring compliance with industry certifications such as ISO 9001. By maintaining effective quality systems, they help organizations deliver consistent, high-quality outcomes and reduce the risk of defects or non-conformance.

What does a quality systems engineer do?

A quality systems engineer conducts frequent and detailed quality checks to make sure the products and processes in a manufacturing setting are consistent and meet both industry and client standards as well as legal demands. In this role, you may monitor processes in various industries, so job duties can vary. However, you always play a role in locating and fixing defects. You check tools and materials, conduct tests, and train employees to meet safety requirements. You also closely document any problems for the engineer, who finds a solution. You follow the entire manufacturing process from beginning to end. In this job, you may work in a lab or an office.

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

To thrive as a Quality Systems Engineer, you need a solid background in quality management principles, process improvement methodologies, and a degree in engineering or a related field. Familiarity with ISO standards, Six Sigma or Lean certifications, and experience with quality management systems (QMS) software are typically required. Strong analytical thinking, attention to detail, and effective communication skills help you excel in cross-functional teams and drive quality initiatives. These competencies ensure compliance, continuous improvement, and the delivery of high-quality products or services.

How does a quality systems engineer typically collaborate with cross-functional teams within an organization?

Quality Systems Engineers often work closely with various departments such as production, engineering, regulatory affairs, and supply chain to ensure that quality management systems are effectively implemented and maintained. They facilitate communication among teams to address compliance issues, resolve process deviations, and implement continuous improvement initiatives. Regular meetings, audits, and training sessions are common ways they collaborate to uphold quality standards and meet regulatory requirements. This collaborative approach helps ensure that quality objectives are integrated throughout all stages of the product lifecycle.

What is the difference between Quality Systems Engineer vs Quality Assurance Engineer?

AspectQuality Systems EngineerQuality Assurance Engineer
CertificationsISO 9001, Six Sigma, ASQ certificationsISO 9001, Six Sigma, ASQ certifications
Work EnvironmentManufacturing, aerospace, automotive, medical devicesManufacturing, software, healthcare, consumer products
ResponsibilitiesDeveloping and maintaining quality management systems, ensuring compliance, process improvementTesting products, identifying defects, ensuring product quality before release

While both roles focus on quality, the Quality Systems Engineer primarily develops and maintains quality management systems and processes, ensuring compliance across the organization. The Quality Assurance Engineer concentrates on testing products and identifying defects to ensure product quality before reaching customers. Both roles often collaborate but serve different stages of the quality management lifecycle.

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For Quality Systems Engineer jobs in California, the most frequently searched job titles are:

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Cities in California with the most Quality Systems Engineer job openings:

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Quality Systems Engineer jobs near you
Infographic showing various Quality Systems Engineer job openings in California as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 10% Part Time, 3% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $102,696 per year, or $49.4 per hour.

Sr. Engineer, Quality Systems

MicroVention

Aliso Viejo, CA • On-site

$100K - $125K/yr

Full-time

Re-posted 9 days ago

Job description


This is a hands-on position in which the Senior Quality Systems Engineer is an active contributor to maintaining and improving quality systems to ensure compliance with global regulatory requirements and ensuring that the quality systems are used effectively to support company quality policy and objectives. Supports the preliminary investigation on CAPA/QAR/audit findings, prepares and analyzes reports/metrics, updates procedures and participates/facilitates Quality Systems related discussion. Drives activities related to Quality System improvements. Job duties:
  • Maintains CAPA process.
  • Partners with the CAPA owners to investigate issues related to audit findings, CAPA and QAR by collaborating with various functions (e.g., R&D, Production, Field Assurance, etc.).
  • Facilitates CAPA Review Board meetings, prepares data to be analyzed for CAPAs, and follows up on actions to drive on-time delivery of committed actions.
  • Leads and supports CAPA owners in understanding and conveying problem statements, conducting thorough root cause investigations and analysis, proposing logical and achievable corrective/preventive actions, and following up to ensure actions are completed on time and effective.
  • Maintains CAPA records to ensure that they are presentable.
  • Supports auditing activities and provides leadership for internal audits conducted by MicroVention associates or consultants.
  • Supports preparation and hosting activities for third party audits including FDA, Notified Body, corporate and international regulatory authorities' audits. Supports follow-up efforts.
  • Prepares and improves quality system metrics, and regularly analyzes trends to drive improvement on overall Quality System program.
  • Partners with associates in other functions to evaluate and analyze the efforts in organizing, documenting and making recommendations to management on quality improvement process.
  • Develops and conducts quality related training, including CAPA process, conducting root cause investigations, and quality improvement processes.
  • Leads the planning and implementation of quality improvement initiatives.
  • Identifies and escalates critical issues that warrant further actions.
  • Creates and/or revises procedures to ensure compliance or drive improvement.
  • Cross-trained as internal auditor to support Internal Audit process.
  • Performs additional responsibilities as assigned.

Qualifications
  1. Bachelor's Degree required or equivalent experience.
  2. A minimum of three (3) to five (5) years of quality assurance/compliance related experience in the medical device industry.
  3. Must be able to handle multiple projects concurrently, have computer experience and have knowledge of FDA Regulations and Application of Good Manufacturing Practices.
  4. Demonstrates understanding of and adherence to Good Documentation Practices.
  5. Demonstrates use of investigation techniques, root cause investigation tools, determining appropriate and effective corrective actions, and how to thoroughly document CAPAs.
  6. Strong interpersonal skills, team player with good problem-solving ability, and good verbal and written communication skills.
  7. Strong analytical and attention to detail skills.
  8. Successful experience working independently and collaboratively, effectively and confidently in a team environment.
  9. Ability to communicate effectively and partner with associates at various levels within the organization.
  10. Proficient with MS Word, Excel, PowerPoint, Visio and Outlook.
Desired Qualifications
  1. Lean Six Sigma, Quality, and/or Project Management related certification, preferred.
  2. Knowledgeable in 21CFR Part 820, ISO13485, ISO14971, EMDR/MDD, MDSAP and CMDCAS regulations.
EEO
We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, national origin, gender, age, religion, disability, sexual orientation, veteran status, marital status or any other characteristics protected by law.
Fair Chance Ordinance
If you are applying to perform work for Terumo Neuro in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Terumo Neuro reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Terumo Neuro will consider for employment qualified job applicants with arrest or conviction records in accordance with the California Fair Chance Act, Los Angeles County Fair Chance Ordinance for Employers, Fair Chance Initiative for Hiring Ordinance, and San Francisco Fair Chance Ordinance.
Salary Range
$100,000 - $125,080 (Financial compensation packages may be higher/lower than listed, & will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs and market demand)

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