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Capa Manager Jobs in California (NOW HIRING)

Abbott

Sr. Quality Systems/CAPA Engineer

Pleasanton, CA

$90K - $180K/yr

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 ...

Abbott

Sr. Quality Systems/CAPA Engineer

Pleasanton, CA · On-site

$90K - $180K/yr

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 ...

Ametek

Quality Manager

Goleta, CA · On-site

Lead and maintain compliance to the AS9100-certified Quality Management System, ensuring continuous improvement of quality policies, procedures, process controls, document control, CAPA, risk ...

Ametek

Quality Manager

Goleta, CA · On-site

Lead and maintain compliance to the AS9100-certified Quality Management System, ensuring continuous improvement of quality policies, procedures, process controls, document control, CAPA, risk ...

Balda C Brewer

QA Compliance Supervisor

Ontario, CA · On-site

$100K - $140K/yr

Plan, schedule, host, and lead internal and external quality audits; drive audit findings through to closure via CAPA management. * Governance & Meetings : Lead and govern the Change Control and CAPA ...

Ionis

Director, PV Systems

Carlsbad, CA · On-site +1

Coordinate with the PM Submissions & CAPA Manager to ensure submission infrastructure is aligned with operational timelines and regulatory reporting obligations. * Flag submission configuration risks ...

ProcessHQ, Inc.

QA/QC Director

Glendale, CA · On-site

$100K - $200K/yr

Experience with investigations, CAPA management, and root cause analysis. * Familiarity with validation, qualification, and stability programs. * Strong understanding of data integrity requirements ...

ProcessHQ, Inc.

QA/QC Director

Glendale, CA · On-site

$100K - $200K/yr

Experience with investigations, CAPA management, and root cause analysis. * Familiarity with validation, qualification, and stability programs. * Strong understanding of data integrity requirements ...

Ionis Pharmaceuticals

Director, PV Systems

Carlsbad, CA · On-site +1

Coordinate with the PM Submissions & CAPA Manager to ensure submission infrastructure is aligned with operational timelines and regulatory reporting obligations. * Flag submission configuration risks ...

ProcessHQ, Inc.

QA/QC Director

Glendale, CA · On-site

$100K - $200K/yr

Experience with investigations, CAPA management, and root cause analysis. * Familiarity with validation, qualification, and stability programs. * Strong understanding of data integrity requirements ...

Expleo

CAPA Network Production

Los Angeles, CA

Le Groupe EXPLEO s'appuie sur 19000 collaborateurs hautement qualifiés qui fournissent des solutions à forte valeur ajoutée dans 30 pays. Expleo vous aide à réaliser vos ambitions et à assurer ...

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Capa Manager information

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$13

$39

$57

How much do capa manager jobs pay per hour?

As of Aug 17, 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 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 the key skills and qualifications needed to thrive as a CAPA manager?

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 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.

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Capa Manager jobs near you
Infographic showing various Capa Manager job openings in California as of August 2026, with employment types broken down into 90% Full Time, and 10% Contract. Highlights an 100% In-person job distribution, with an average salary of $81,857 per year, or $39.4 per hour.

Sr. Quality Systems/CAPA Engineer

Abbott

Pleasanton, CA

$90K - $180K/yr

Full-time

Medical, Retirement

Re-posted 22 days ago

Abbott rating

7.8

Company rating: 7.8 out of 10

Based on 138 frontline employees who took The Breakroom Quiz

178th of 540 rated manufacturers

Job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.JOB DESCRIPTION:
Job Description

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to:

  • Career development with an international company where you can grow the career you dream of.

  • Employees can qualify forfree medical coverage in ourHealth Investment Plan (HIP) PPOmedical plan in the next calendar year.

  • An excellent retirement savings plan with a high employer contribution.

  • Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree.

  • A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.

  • A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

The Senior Quality Systems Engineer assures products conform to quality standards and establishes compliance with the quality system. Responsible for maintaining a strong collaborative partnership with cross-functional team members that facilitates organizational success. The position employs an individual skilled in advance quality assurance techniques with an in-depth understanding of the ISO 13485 Quality Standard and US 21 CFR 820 QSR. Areas of focus will include improving quality system infrastructure, performance metrics and ISO, FDA and GMP compliance.

What You'll Work On

  • Assure compliance with corporate and divisional requirements regarding metrics reporting for the Management Controls / Management Review and CAPA quality systems.
  • Assure the collection, compiling, reporting and dissemination of key quality and compliance metrics/data are completed within the requiring timing.
  • Complete trend analysis of data as appropriate to ensure proper actions can be determined or assessed.
  • Perform and assure timely follow-up activities in support of key quality and compliance metric/data goals and policy/procedural requirements
  • 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 opportunities to apply, continuously improve, and redefine quality systems and controls product-related processes in accordance with applicable internal, domestic and international quality regulations, US 21 CFR 820 (QSR), ISO 13485, etc.
  • Represent Quality Systems as required in support of cross-functional projects
  • Assist in company preparations for hosting external audits
  • Participate in external and internal audits
  • Assists management teams to ensure timely closure of audit observations. Lead non-conformance investigation teams to identify root causes and effective CAPAs
  • Lead, coach, and mentor non-exempt and entry level exempt personnel on quality principles and procedures
  • Function as part of risk assessment teams to identify product, quality system and compliance requirements.
  • Function as part of special project teams to identify compliance gaps and develop and execute strategies to close gaps.

Required Qualifications :

  • Bachelor's degree in engineering or Technical Field
  • Minimum 5or more years of Engineering experience and demonstrated use of Quality tools/methodologies
  • knowledge of FDA820, GMP, ISO 13485, and ISO 14971

Preferred Qualifications:

  • Project management and leadership skills, including the demonstrated ability to lead multi-departmental project teams and resolve quality-related issues
  • Internal and External Audit experience
  • MS or higher degree in a technical discipline
  • Advanced computer skills, including statistical/data analysis and report writing skills
  • medical device industry experience
  • ASQ CQE or CQA certification

Apply Now

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott, and on Twitter @AbbottNews.

The base pay for this position is

$90,000.00 - $180,000.00

In specific locations, the pay range may vary from the range posted.

JOB FAMILY:Operations QualityDIVISION:HF Heart FailureLOCATION:United States > Pleasanton : 6101 Stoneridge DrADDITIONAL LOCATIONS:WORK SHIFT:StandardTRAVEL:Yes, 10 % of the TimeMEDICAL SURVEILLANCE:NoSIGNIFICANT WORK ACTIVITIES:Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdfEEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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