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Capa Manager Jobs (NOW HIRING)

CAPA Process Analyst II

Gretna, LA · On-site

$29 - $32/hr

This role focuses on managing CAPA activities, ensuring compliance with QMS procedures, and maintaining audit-ready documentation using EQMS platforms. The analyst will collaborate with cross ...

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Capa Manager information

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How much do capa manager jobs pay per hour?

As of Jun 19, 2026, the average hourly pay for capa manager in the United States is $40.19, according to ZipRecruiter salary data. Most workers in this role earn between $30.53 and $47.36 per hour, depending on experience, location, and employer.

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 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.

More about Capa Manager jobs
What cities are hiring for Capa Manager jobs? Cities with the most Capa Manager job openings:
What states have the most Capa Manager jobs? States with the most job openings for Capa Manager jobs include:
Infographic showing various Capa Manager job openings in the United States as of June 2026, with employment types broken down into 2% Full Time, 90% Part Time, 7% Contract, and 1% Nights. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $83,593 per year, or $40.2 per hour.
Sr Quality Analysis - CAPA Mentor

Sr Quality Analysis - CAPA Mentor

Boston Scientific

Valencia, CA

$89K - $121K/yr

Full-time

Posted 19 hours ago


Boston Scientific rating

8.5

Company rating: 8.5 out of 10

Based on 119 frontline employees who took The Breakroom Quiz

32nd of 518 rated manufacturers


Job description

Recruiter: Spencer Gregory Hale

Sr Quality Analysis - CAPA Mentor

About the role:

This role provides site‑level 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 cross‑functional teams through nonconforming events and the development, implementation, and verification of corrective and preventive actions.
  • Provide subject‑matter expertise on structured problem‑solving 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 decision‑making.
  • 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 cross‑functional teams through nonconforming events and CAPA implementation.
  • Strong written and verbal communication skills with a high level of attention to detail.
  • Proven problem‑solving, organizational, and execution skills.

 

Preferred Qualifications:

  • Broad working knowledge of quality systems and processes (e.g., CAPA, NCRs, audits, complaints).
  • Quality‑related certifications (e.g., ISO 13485, AS9100).
  • Subject‑matter 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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