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Capa Engineer Jobs in California (NOW HIRING)

Product Quality Engineer (PQE)

San Jose, CA · On-site

$84K - $109K/yr

Drive root cause analysis (RCA) and corrective action (CAPA) across product engineering, manufacturing, reliability engineering, and test engineering teams * Manage failure analysis (FA) requests and ...

QP Engineer

Santa Clara, CA · On-site

$120K - $140K/yr

Coordinate customer complaints, 8D/CAPA responses, internal/customer/QMS audits, audit findings ... Bachelor's degree in Engineering, Quality, Business Administration, or a related field required.

We are currently looking for a Validation Engineer to work for a leading Greater Los Angeles area ... Familiarity with deviation investigations, CAPA processes, and audit responses. * Basic vendor ...

Sr. Process Engineer

San Diego, CA · On-site

$110K - $142K/yr

Lead Corrective and Preventive Action (CAPA) initiatives to eliminate recurring issues and ... Partner with quality engineering to implement corrective and preventive actions (CAPA)

Manufacturing Engineer

Northridge, CA · On-site

$78K - $101K/yr

Maintain technical documentation and engineering records CAPA, Quality, and Compliance * Support investigations, deviations, and CAPAs. * Complete assigned quality actions by committed due dates.

Manufacturing Engineer

Northridge, CA · On-site

$78K - $101K/yr

Maintain technical documentation and engineering records CAPA, Quality, and Compliance * Support investigations, deviations, and CAPAs. * Complete assigned quality actions by committed due dates.

Quality Engineer

San Francisco, CA · On-site

$150 - $200/hr

Quality Engineer Will be a key contributor to Ouster's mission by driving world‑class quality ... Failure Analysis & Corrective Action (CAPA): * Lead and document Root Cause Analysis (RCA) for ...

Manufacturing Engineer

Northridge, CA · On-site

$78K - $101K/yr

Maintain technical documentation and engineering records CAPA, Quality, and Compliance * Support investigations, deviations, and CAPAs. * Complete assigned quality actions by committed due dates.

Quality Engineer

Anaheim, CA · On-site

$75K - $97K/yr

For more than 20 years, ACT has engineered and manufactured innovative technologies that solve ... Support manufacturing and development teams with process mapping, controls, SOPs, CAPA, inspections ...

Manufacturing Engineer

Northridge, CA · On-site

$78K - $101K/yr

Maintain technical documentation and engineering records CAPA, Quality, and Compliance * Support investigations, deviations, and CAPAs. * Complete assigned quality actions by committed due dates.

Showing results 21-40

Capa Engineer information

See California salary details

$38.5K

$100.4K

$135.7K

How much do capa engineer jobs pay per year?

As of Sep 11, 2026, the average yearly pay for capa engineer in California is $100,420.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,900.00 and $115,000.00 per year, depending on experience, location, and employer.

What is a CAPA engineer?

A CAPA (Corrective and Preventive Action) Engineer is responsible for identifying, investigating, and resolving quality issues in manufacturing or engineering processes. They analyze root causes of defects, implement corrective measures, and develop preventive strategies to ensure compliance with industry regulations. CAPA Engineers work closely with cross-functional teams to improve product quality, streamline processes, and maintain regulatory compliance. They also document findings, track action plans, and support continuous improvement initiatives to reduce future risks.

What are the main daily responsibilities of a CAPA engineer?

A CAPA Engineer's daily responsibilities typically include investigating potential or actual nonconformities, conducting root cause analyses, and developing corrective and preventive action plans to resolve and prevent future issues. They also collaborate closely with cross-functional teams such as manufacturing, quality assurance, and regulatory affairs to ensure solutions are practical and compliant with industry standards. Additionally, CAPA Engineers monitor the progress and effectiveness of implemented actions, prepare documentation for audits, and participate in continuous process improvement initiatives. This role is crucial for maintaining the highest quality standards and ensuring compliance in regulated industries such as medical devices or pharmaceuticals.

What are the key skills and qualifications needed to thrive in the CAPA engineer position, and why are they important?

To thrive as a CAPA Engineer, you need a solid background in quality engineering, root cause analysis, and process improvement, typically supported by a degree in engineering or a related technical field. Familiarity with CAPA management systems, quality standards such as ISO 13485 or ISO 9001, and tools like Six Sigma or FMEA is highly valuable. Strong problem-solving abilities, attention to detail, and effective communication skills distinguish top performers in this role. These competencies ensure effective identification, documentation, and resolution of quality issues, helping organizations maintain regulatory compliance and deliver high-quality products.

What are the most commonly searched types of Capa Engineer jobs in California?

The most popular types of Capa Engineer jobs in California are:

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

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

What cities in California are hiring for Capa Engineer jobs?

Cities in California with the most Capa Engineer job openings:

Infographic showing various Capa Engineer job openings in California as of September 2026, with employment types broken down into 80% Full Time, and 20% Contract. Highlights an 95% In-person, and 5% Hybrid job distribution, with an average salary of $100,420 per year, or $48.3 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 6 days ago


Olympus Corporation Of The Americas rating

8.1

Company rating: 8.1 out of 10

Based on 20 frontline employees who took The Breakroom Quiz


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, Cafe, 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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