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Quality System Engineer Jobs in California (NOW HIRING)

Quality Systems Engineer

Torrance, CA · On-site

$100 - $125/hr

Quality Systems Engineer The Quality Systems Engineer will be responsible for managing Castelion ... Responsibilities Quality Management System (QMS) Oversight * Manage and maintain Castelion's non ...

This is a hands-on position in which the Senior Quality Systems Engineer is an active contributor ... Drives activities related to Quality System improvements. Job duties: * Maintains CAPA process.

System Engineer

Lathrop, CA · On-site

$80 - $100/hr

The System Engineer focuses on troubleshooting, maintaining, and stabilizing complex ... quality, safety and system performance. What you'll do * Monitor and maintain the health of ...

System Engineer Pay Rate: $48 - $68.66/hr. Location: Irvine, CA Area Code: 949 Zip Code: 92618 ... Our overriding goal is to provide quality staffing solutions that help people, organizations, and ...

The System Engineer focuses on troubleshooting, maintaining, and stabilizing complex electro ... quality, safety and system performance.   What you'll do * Monitor and maintain the health of ...

The System Engineer focuses on troubleshooting,maintaining, and stabilizing complex electro ... class quality,safetyand system performance. Whatyou'lldo * Monitor andmaintainthe health of ...

The System Engineer focuses on troubleshooting, maintaining, and stabilizing complex electro ... quality, safety and system performance. What you'll do * Monitor and maintain the health of ...

System Engineer

San Jose, CA · On-site

$84K - $95K/yr

Ensure all system deliverables meet quality, schedule, and performance targets * Collaborate closely with Engineering, Manufacturing, Sales, Component Management, and Lab teams to drive cohesive ...

System Engineer

San Jose, CA · On-site

$84K - $95K/yr

Ensure all system deliverables meet quality, schedule, and performance targets * Collaborate closely with Engineering, Manufacturing, Sales, Component Management, and Lab teams to drive cohesive ...

System Quality Engineer

Sunnyvale, CA · On-site

$125 - $150/hr

System 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 technologies ...

The System Engineer focuses on troubleshooting, maintaining, and stabilizing complex electro ... quality, safety and system performance. What you'll do * Monitor and maintain the health of ...

The System Engineer focuses on troubleshooting, maintaining, and stabilizing complex electro ... quality, safety and system performance.   What you'll do * Monitor and maintain the health of ...

As a Quality Systems Engineer, you will have ownership of policies and procedures that govern the way the entire company functions and operates. This is an extremely influential role for people who ...

Showing results 21-40

Quality System Engineer information

See California salary details

$27

$49

$79

How much do quality system engineer jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for quality system 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 system engineer?

Quality System Engineers are professionals responsible for developing, implementing, and maintaining quality management systems within organizations. They ensure that products and processes meet established quality standards and regulatory requirements. Their duties often include auditing internal processes, analyzing data to identify areas for improvement, and collaborating with various departments to implement corrective actions. Quality System Engineers play a crucial role in ensuring continuous improvement and compliance with industry standards such as ISO 9001.

How does a quality system engineer typically collaborate with cross-functional teams to ensure compliance and continuous improvement?

Quality System Engineers often work closely with teams such as manufacturing, regulatory affairs, R&D, and supply chain to maintain and improve quality management systems. They facilitate audits, coordinate corrective and preventive actions (CAPA), and provide training on quality standards. Regular meetings and process reviews help ensure that all departments are aligned with compliance requirements and best practices. This collaborative approach not only supports regulatory compliance but also drives continuous improvement initiatives across the organization.

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

To thrive as a Quality System Engineer, you need expertise in quality management systems (QMS), process improvement, and a relevant engineering degree or certification such as Six Sigma or ISO 9001 auditor credentials. Familiarity with tools like root cause analysis software, statistical process control (SPC), and document management systems is typically required. Strong analytical thinking, problem-solving, and effective communication skills help you collaborate across departments and drive continuous improvement. These skills ensure compliance with standards, enhance product reliability, and support operational excellence within an organization.

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

AspectQuality System EngineerQuality Assurance Engineer
CertificationsISO 9001 Lead Auditor, ASQ CQEASQ CQE, Six Sigma Green/Black Belt
Work EnvironmentManufacturing, ISO compliance, process improvementProduct testing, process validation, defect prevention
Industry UsageManufacturing, aerospace, automotiveSoftware, electronics, manufacturing

Both roles focus on quality but differ in scope. The Quality System Engineer primarily develops and maintains quality management systems, ensuring compliance with standards like ISO 9001. The Quality Assurance Engineer concentrates on testing products and preventing defects during production. While overlapping in quality principles, their daily tasks and focus areas vary based on organizational needs.

What are popular job titles related to Quality System Engineer jobs in California?

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

What job categories do people searching Quality System Engineer jobs in California look for?

The top searched job categories for Quality System Engineer jobs in California are:

Infographic showing various Quality System 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.

Senior Engineer, Quality Systems

San Jose, CA • On-site

Olympus Corporation of the Americas
Medical Equipment and Supplies Manufacturing • 10K+ employees

$103K - $140K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 4 days ago


Olympus Corporation Of The Americas rating

8.2

Company rating: 8.2 out of 10

Based on 19 frontline employees who took The Breakroom Quiz

137th of 499 rated machine equipment manufacturers


Job description

Working Location: California, San Jose 

Workplace Flexibility: Onsite

For more than 100 years, Olympus has focused on making people’s lives healthier, safer and more fulfilling. ​

Every day, we live by our philosophy, True to Life, by advancing medical technologies and elevating the standard of patient care so people everywhere can fulfill their desires, dreams, and lives.

Our five Core Values empower us to achieve Our Purpose: 

Patient Focus, Integrity, Innovation, Impact and Empathy. 

Learn more about Life at Olympus: https://www.olympusamerica.com/careers.

Job Description

The Quality Systems Engineer will be responsible for the continued development and maintenance of the Quality Assurance systems to ensure compliance with the requirements of 21 CFR Part 820 Quality Management System Regulation (QMSR/QSR), ISO 13485, and other quality standards. This individual contributor role will lead Quality Management System (QMS) compliance initiatives, policy implementation, risk assessments, remediation actions, audit readiness, and cross-functional quality system projects. In addition, this individual contributor will provide technical support to align functions, sites, regions, and business units.

Job Duties
  • Assist with routine and periodic internal and external audits to ensure QMSR / ISO compliance is maintained at all levels of the organization.
  • Review internal audit responses to ensure they are consistent with policy. Support all departments on the successful execution of the internal audit schedule and policy. Provides quality system support during internal audits, external audits and inspections.
  • Support Document and Change Control processes and systems including the ongoing maintenance and improvement of database reports and ancillary systems.
  • Support CAPA and Audit processes and systems including the ongoing maintenance and improvement of database reports and ancillary systems.
  • Serve as the CAPA Coordinator, backup CAPA Lead, and CAPA mentor for CAPA Owners.
  • Support in defining implementation approach, deliverables, governance, risks, success criteria, and escalation pathways.
  • Provides review of QMS changes, procedures, training plans, records, dashboards, and implementation evidence. Provides support and review of Quality Management Reviews (QMRs).
  • Support and take lead (as needed) of cross-functional meetings, align stakeholders, remove barriers, and drive action closure.
  • Drive process standardization, compliance technology adoption, digital workflow improvements, and continuous improvement (or 6-sigma kaizen projects). Maintain and improve QMS processes, procedures, and systems to ensure continued compliance with documented requirements and standards.
  • Support continuous improvement projects related to the development, maintenance, and improvement of Olympus quality management systems. Support quality system data collection and provide regular reports to management on quality system topics such as Audit status, CAPAs, Deviations, Nonconformances, Validations, and Change Controls.
  • Develop curriculum to provide training and support for established quality systems.
  • Perform other duties as required.
Job Qualifications

Required:

  • Bachelor’s degree in Engineering, Life Sciences, Quality, Regulatory Affairs, Compliance, or related discipline.
  • Training in medical device QMS requirements, validations (hardware and software), quality planning, audit support, risk management, project leadership, remediation management, and Good Documentation Practices required.
  • Minimum of 5 years of experience in Quality Systems, Quality Engineering, Compliance, Regulatory, Engineering, Operations, or a related field.
  • Working knowledge of medical device QMS requirements and regulated change implementation.
  • Experience leading quality plans, QMS remediation, policy implementation, regulatory inspection readiness, process standardization, compliance technology implementation (validations).
  • Experience mentoring cross-functional team members on quality concepts and preparing compliance updates to management.
  • Strong technical writing, risk-based thinking, stakeholder management, executive communication, and project leadership skills.
  • Ability to coach and influence cross-functional teams without direct authority.
  • Ability to translate regulatory and procedural requirements into practical implementation plans.
  • In office work environment.
  • Frequent cross-functional engagement across sites and process ownership teams.
  • Work may include time-sensitive deliverables, audit readiness support, inspection response, remediation tracking, and leadership reporting.
  • Requires the ability to manage multiple priorities and support business needs across time zones.

Preferred:

  • Certifications such as ASQ CQA, CQE, CMQ/OE, RAC, Lean Six Sigma, or PMP preferred.

Why join Olympus?

We offer a holistic employee experience supporting personal and professional well-being through meaningful work, equitable offerings, and a connected culture.

Equitable Offerings you can count on:

  • Competitive salaries, annual bonus and 401(k)* with company match

  • Comprehensive medical, dental, vision coverage effective on start date

  • 24/7 Employee Assistance Program

  • Free live and on-demand Wellbeing Programs

  • Generous Paid Vacation and Sick Time

  • Paid Parental Leave and Adoption Assistance*

  • 12 Paid Holidays

  • On-Site Child Daycare, Café, Fitness Center**

Connected Culture you can embrace:

  • Work-life integrated culture that supports an employee centric mindset

  • Offers onsite, hybrid and field work environments

  • Paid volunteering and charitable donation/match programs

  • Employee Resource Groups

  • Dedicated Training Resources and Learning & Development Programs

  • Paid Educational Assistance

*US Only

**Center Valley, PA and Westborough, MA

Are you ready to be a part of our team?

Learn more about our benefits and incentives: https://www.olympusamerica.com/careers/benefits-perks.

The anticipated base pay range for this full-time position in this location is $104,622.00 - $141,240.00 / year, plus potential for annual bonus (subject to plan eligibility and other requirements). 

Olympus considers a variety of factors when determining actual compensation for this position, including level of experience, working location, and relevant education and certifications.

At Olympus, we are committed to Our Purpose of making people’s lives healthier, safer and more fulfilling. As a global medical technology company, we partner with healthcare professionals to provide best-in-class solutions and services for early detection, diagnosis and minimally invasive treatment, aiming to improve patient outcomes by elevating the standard of care in targeted disease states. 

For more than 100 years, Olympus has pursued a goal of contributing to society by producing products designed with the purpose of delivering optimal outcomes for its customers around the world.

Headquartered in Tokyo, Japan, Olympus employs more than 31,000 employees worldwide in nearly 40 countries and regions. Olympus Corporation of the Americas, a wholly owned subsidiary of Olympus Corporation, is headquartered in Center Valley, Pennsylvania, USA, and employs more than 5,200 employees throughout locations in North and South America. For more information, visit www.olympusamerica.com.

You Belong at Olympus

We are deeply committed to fostering a respectful, fair, and welcoming workplace for all individuals, perspectives, and lifestyles. We believe in fostering a non-discriminatory, inclusive work environment where everyone feels a sense of belonging, in full compliance with legal standards. Empathy and unity are core to our company culture, empowering employees to contribute fully and flourish. We warmly encourage all who wish to bring their talents to Olympus to apply.

Applicants Requesting Accommodations: Olympus is committed to the full inclusion of all qualified individuals. As part of this commitment, Olympus will ensure that persons with disabilities are provided reasonable accommodations for the hiring process. If reasonable accommodation is needed, please contact OCAAccommodations@olympus.com. If your disability impairs your ability to email, you may call our HR Compliance Manager at 1-888-Olympus (1-888-659-6787).

Let’s realize your potential, together.

It is the policy of Olympus to extend equal employment and advancement opportunity to all applicants and employees without regard to race, color, national origin (including language use restrictions), citizenship status, religious creed (including dress and grooming practices), age, sex (including pregnancy, childbirth, breastfeeding, medical conditions related to pregnancy, childbirth and/or breastfeeding), gender, gender identity and expression, sexual orientation, marital status, disability (physical or mental) and/or a medical condition, genetic information, ancestry, veteran status or service in the uniformed services, and any other characteristic protected by applicable federal, state or local law.

 

Posting Notes: || United States (US) || California (US-CA) || San Jose || Quality & Regulatory Affairs (QA/RA) 


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