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Capa Jobs in California (NOW HIRING)

Develop and provide data and analysis in support of Management Controls / Management Review and CAPA Quality Systems * Identify and implement opportunities for continuous improvement * Identify ...

Develop and provide data and analysis in support of Management Controls / Management Review and CAPA Quality Systems * Identify and implement opportunities for continuous improvement * Identify ...

Develop and provide data and analysis in support of Management Controls / Management Review and CAPA Quality Systems * Identify and implement opportunities for continuous improvement * Identify ...

Company Description Deegit Inc. Project management activities related to CAPAs and other Quality activities that include: • Planning and tracking of project activities. • Ensuring adherence to ...

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Quality Manager

Hawthorne, CA · On-site

$120K - $150K/yr

CAPA, NCR, and Root Cause • Lead structured root‐cause investigations using 5‐Why, Fishbone, DMAIC, or similar tools. • Drive timely and effective CAPA implementation, verification, and ...

Compliance Audit Analyst

Carlsbad, CA · On-site

$97K - $98K/yr

Manage CAPA workstream, CAPA investigations, CAPA & compliance audit trending of quality data streams. 2. Develop & establish continuously improving plans for site CAPA system, quality assurance ...

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Capa information

See California salary details

$14

$41

$68

How much do capa jobs pay per hour?

As of Jul 13, 2026, the average hourly pay for capa in California is $41.29, according to ZipRecruiter salary data. Most workers in this role earn between $31.31 and $48.02 per hour, depending on experience, location, and employer.

What are the typical daily responsibilities of a CAPA specialist?

A CAPA specialist is responsible for investigating quality issues, identifying root causes, and implementing corrective and preventive actions to ensure ongoing compliance and product integrity. Their typical day involves reviewing nonconformance reports, collaborating with cross-functional teams, documenting findings, and tracking the progress of CAPA initiatives using specialized software. CAPA specialists also prepare reports for audits and may facilitate meetings to drive continuous improvement activities. This role often requires balancing multiple projects and deadlines in a regulated environment, making organizational and communication skills crucial for success.

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

To thrive as a CAPA (Corrective and Preventive Action) specialist, you need expertise in quality management systems, root cause analysis, and compliance with industry standards, typically backed by a degree in engineering, life sciences, or a related field. Familiarity with CAPA software, regulatory frameworks (such as ISO 13485 or FDA 21 CFR Part 820), and document control systems is essential. Strong analytical thinking, attention to detail, and effective communication skills are vital soft skills for this role. These skills ensure effective problem-solving and sustained compliance, which are essential for maintaining product quality and meeting regulatory requirements.

What is a CAPA job?

A CAPA (Corrective and Preventive Action) job involves identifying, investigating, and resolving quality issues in industries like manufacturing, healthcare, and pharmaceuticals. CAPA professionals analyze root causes of defects or process failures and implement corrective actions to prevent recurrence. They ensure compliance with regulatory standards, document findings, and improve overall quality management systems. Their role is critical in maintaining product safety, efficiency, and regulatory adherence.

What are the most commonly searched types of Capa jobs in California? The most popular types of Capa jobs in California are:
What job categories do people searching Capa jobs in California look for? The top searched job categories for Capa jobs in California are:
What cities in California are hiring for Capa jobs? Cities in California with the most Capa job openings:
Infographic showing various Capa job openings in California as of July 2026, with employment types broken down into 89% Full Time, 4% Part Time, 2% Temporary, 4% Contract, and 1% Nights. Highlights an 94% Physical, 3% Hybrid, and 3% Remote job distribution, with an average salary of $85,889 per year, or $41.3 per hour.
Sr Quality Analysis - CAPA Mentor

Sr Quality Analysis - CAPA Mentor

Boston Scientific

Valencia, CA • On-site

$89K - $121K/yr

Other

Re-posted 25 days ago


Boston Scientific rating

8.5

Company rating: 8.5 out of 10

Based on 119 frontline employees who took The Breakroom Quiz

34th of 527 rated manufacturers


Job description

Recruiter: Spencer Gregory Hale

Sr Quality Analysis - CAPA Mentor

About the role:

This role provides sitelevel CAPA mentorship, oversight, and approval support across the quality system. The CAPA Mentor partners with CAPA owners, project teams, and Quality leadership to ensure timely, compliant, and effective corrective and preventive actions, while driving continuous improvement and risk reduction.

 

Your responsibilities will include:

Key responsibilities include, but are not limited to, the following:

  • Manage and oversee the CAPA portfolio, including monitoring, tracking, and reporting CAPA health, compliance, and performance metrics to Quality leadership.
  • Serve as a CAPA Mentor by coaching and guiding crossfunctional teams through nonconforming events and the development, implementation, and verification of corrective and preventive actions.
  • Provide subjectmatter expertise on structured problemsolving methodologies and effective execution of the CAPA process across all phases.
  • Partner with CAPA owners to ensure CAPA records are compliant with global and local procedures, clearly written, logically structured, and aligned with the intent of each CAPA activity, including appropriate documentation of rationale and decisionmaking.
  • Collaborate with Quality Assurance, Project Management, and functional leaders to identify systemic quality issues and drive continuous improvement initiatives.
  • Provide CAPA status updates, milestone tracking, and risk assessments to Project Managers and stakeholders for assigned projects.
  • Review and approve CAPA records and phases, as applicable, ensuring compliance with global CAPA requirements and quality system expectations.
  • Participate in Community of Practice meetings for nonconforming events and CAPA as needed.
  • Participate in projects as needed.

What we are looking for in you:

Minimum Qualifications:

  • Bachelor's degree required.
  • Minimum of 5 years of experience supporting nonconforming events and CAPA within a regulated environment.
  • Experience working in regulated industries (e.g., FDA, ISO standards, EU MDR, ISO 13485).
  • Demonstrated experience leading or mentoring crossfunctional teams through nonconforming events and CAPA implementation.
  • Strong written and verbal communication skills with a high level of attention to detail.
  • Proven problemsolving, organizational, and execution skills.

 

Preferred Qualifications:

  • Broad working knowledge of quality systems and processes (e.g., CAPA, NCRs, audits, complaints).
  • Qualityrelated certifications (e.g., ISO 13485, AS9100).
  • Subjectmatter expertise in CAPA regulations and nonconforming event management.

Requisition ID: 625300 

Minimum Salary: $ 89200 

Maximum Salary: $ 169500 

The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) - see www.bscbenefitsconnect.com-will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above.

Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).

For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.

Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.

Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions.  This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement.  The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.  


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