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Capa Manager Jobs in California (NOW HIRING)

Quality Operations Manager

Fremont, CA · On-site

$10K - $163K/yr

... CAPA. * Manages- calibration activities for instrumentation, measurement and test equipment ... resource optimization, and incoming material and outgoing product acceptance activities, resource ...

... CAPA. * Manages- calibration activities for instrumentation, measurement and test equipment ... resource optimization, and incoming material and outgoing product acceptance activities, resource ...

Key Responsibilities: • Supplier Qualification & Evaluation • Supplier Audits & Performance Monitoring • SCAR & CAPA Management • Root Cause Analysis & Corrective Actions • FDA & ISO 13485 ...

Temperature Excursion Management & CAPA * Validated Lanes & Packaging Systems * Pharmaceutical DC Operations * Audit Readiness & Regulatory Inspections * Deviation Documentation & QA Collaboration ...

Project management activities related to CAPAs and other Quality activities that include: • Planning and tracking of project activities. • Ensuring adherence to Design control process in project ...

Temperature Excursion Management & CAPA * Validated Lanes & Packaging Systems * Pharmaceutical DC Operations * Audit Readiness & Regulatory Inspections * Deviation Documentation & QA Collaboration ...

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Capa Manager information

See California salary details

$13

$39

$57

How much do capa manager jobs pay per hour?

As of Jul 13, 2026, the average hourly pay for capa manager in California is $39.35, according to ZipRecruiter salary data. Most workers in this role earn between $29.89 and $46.37 per hour, depending on experience, location, and employer.

What is the role of a Capa specialist?

A CAPA (Corrective and Preventive Action) specialist is responsible for investigating quality issues, implementing corrective actions, and preventing recurrence of problems within a quality management system. They analyze data, ensure compliance with regulations, and often use tools like root cause analysis to improve product and process quality.

What does a CAPA Manager do?

A CAPA (Corrective and Preventive Action) Manager is responsible for overseeing an organization's CAPA process to ensure compliance with quality and regulatory requirements. They investigate quality issues, identify root causes, and implement corrective and preventive measures to prevent recurrence. CAPA Managers work closely with cross-functional teams to improve processes, maintain regulatory compliance, and enhance overall product or service quality.

What is a capa coordinator?

A CAPA (Corrective and Preventive Action) coordinator is responsible for managing and overseeing the CAPA process within a quality management system. They investigate quality issues, implement corrective actions, and ensure compliance with regulatory standards, often using tools like root cause analysis and tracking software. This role requires strong organizational skills and knowledge of quality regulations such as ISO or FDA requirements.

What is the highest paying manager position?

The highest paying manager positions are typically executive roles such as Chief Executive Officer (CEO), Chief Operating Officer (COO), and Chief Financial Officer (CFO), which often have salaries exceeding several hundred thousand dollars annually. In some industries, specialized managerial roles like Vice President or Director of certain departments can also command high compensation, especially with bonuses and stock options included.

What are some common challenges a CAPA Manager faces, and how are they typically addressed?

One common challenge CAPA Managers face is ensuring timely and thorough investigations into quality issues while coordinating input from multiple departments. Balancing the need for fast resolution with the rigor required for regulatory compliance can be demanding, especially in highly regulated industries like pharmaceuticals or medical devices. Successful CAPA Managers often address these challenges through clear process documentation, effective project management, and fostering strong collaboration among stakeholders. By leveraging root cause analysis tools and maintaining open communication, they help create a continuous improvement culture that benefits both the organization and its customers.

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

To thrive as a CAPA Manager (Corrective and Preventive Action Manager), you typically need a background in quality assurance, strong analytical and problem-solving abilities, and experience with regulatory compliance, often supported by a degree in a science or engineering field. Familiarity with quality management systems (QMS), risk management tools, root cause analysis methodologies (such as 5 Whys or Fishbone diagrams), and industry certifications like Six Sigma or ISO 9001 are highly valued. Outstanding candidates demonstrate excellent communication, leadership, and organizational skills to effectively drive cross-functional teams and ensure timely resolution of quality issues. These skills are crucial for identifying, addressing, and preventing compliance gaps or product issues, thereby maintaining high standards and avoiding costly regulatory penalties.

What does a capa manager do?

A CAPA (Corrective and Preventive Action) manager oversees the implementation of processes to identify, investigate, and resolve quality issues within an organization. They analyze root causes, develop action plans, and ensure compliance with regulatory standards, often using quality management systems and tools like CAPA software. The role requires strong problem-solving skills and knowledge of industry regulations such as ISO or FDA standards.
What are popular job titles related to Capa Manager jobs in California? For Capa Manager jobs in California, the most frequently searched job titles are:
What cities in California are hiring for Capa Manager jobs? Cities in California with the most Capa Manager job openings:
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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