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Capa Manager Jobs (NOW HIRING)

At CAPA, we are committed to inspiring and transforming lives through the power of the performing arts. With a rich history and a dynamic vision for the future, we manage iconic theaters, host world ...

At CAPA, we are committed to inspiring and transforming lives through the power of the performing arts. With a rich history and a dynamic vision for the future, we manage iconic theaters, host world ...

CAPA Engineer II

Princeton, NJ

$71.30K - $97.75K/yr

The CAPA Engineer II is expected to manage assigned activities with moderate independence while escalating risks, delays, and quality concerns to the Sr. Manager, CAPA, NC and Metrics. Essential ...

CAPA Engineer II

Princeton, NJ · On-site

$71.30K - $97.75K/yr

The CAPA Engineer II is expected to manage assigned activities with moderate independence while escalating risks, delays, and quality concerns to the Sr. Manager, CAPA, NC and Metrics. Essential ...

Lead GRAIL's CAPA program within the Quality Management System (QMS), including planning and running CAPA Review Board meetings, overseeing program and individual CAPA activities to ensure on-time ...

Capa General Manager Who We Look For: We are looking for an individual who can provide support in Capa, our Spanish-influenced cuisine, rooftop steakhouse and bar who has 2 years' experience working ...

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 ...

Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services ... Investigation & CAPA Specialist Position Summary We are seeking an experienced Investigation and ...

Sr. CAPA Quality Engineer

Alameda, CA

$100.30K - $136K/yr

Consistent and accurate glucose monitoring is the foundation of any diabetes management plan, and ... The position will be responsible for driving CAPA projects through its entire life cycle, mentor ...

Sr. CAPA Quality Engineer

Alameda, CA · On-site

$100.30K - $136K/yr

Consistent and accurate glucose monitoring is the foundation of any diabetes management plan, and ... The position will be responsible for driving CAPA projects through its entire life cycle, mentor ...

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Capa Manager information

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How much do capa manager jobs pay per hour?

As of May 29, 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 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 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 is a CAPA manager?

A CAPA manager oversees the Corrective and Preventive Actions process within an organization to identify, investigate, and resolve quality issues or non-conformities. They ensure compliance with regulatory standards, often using quality management tools, and coordinate cross-functional teams to implement effective solutions.

What job makes $10,000 a month without a degree?

A Capa Manager, or Corrective and Preventive Action Manager, can earn around $10,000 monthly by overseeing quality management systems in manufacturing or healthcare environments. Success in this role depends on experience, industry knowledge, and strong organizational skills, often without requiring a formal degree but emphasizing certifications and practical expertise.
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 May 2026, with employment types broken down into 98% Full Time, and 2% Contract. Highlights an 100% Physical job distribution, with an average salary of $83,593 per year, or $40.2 per hour.
Senior Quality Manager, CAPA & NC

Senior Quality Manager, CAPA & NC

Integra LifeSciences

Princeton, NJ • On-site

$125.35K - $172.50K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 6 days ago


Integra LifeSciences rating

9.3

Company rating: 9.3 out of 10

Based on 7 frontline employees who took The Breakroom Quiz


Job description

Changing lives. Building Careers.
Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what's possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.
SUMMARY
The Senior Quality Manager, CAPA and Nonconformances (NC) has responsibilities to develop and lead the implementation plan of Integra's Global Quality Management System Compliance Processes (CAPA and Nonconformances). Work with process and Quality Operations leadership to drive consistent best practices for CAPA and NC, Management Review and Metrics and establish global oversight. Deploy CAPA and NC processes and digital systems that improve compliance, efficiencies, and overall effectiveness. Responsible for partnering with global quality leaders to develop processes and metrics that result in attaining the company's improvement objectives and growth strategies.
ESSENTIAL DUTIES AND RESPONSIBILITIES
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
  • Establish and maintain the Corporate CAPA board to address company-wide Corrective and Preventive actions. Includes the identification of issues, their investigation, and implementation of actions to address nonconformances and verification of the effectiveness of the actions.
  • Maintain the Global Nonconformance (NC) process to ensure compliance in areas of investigation, effectiveness, timeliness, quality and thoroughness of content. Collaborate with process owners and stakeholders in Corporate, division and site to ensure the program is compliant, executable, and continuously improves.
  • Lead the reporting of quality system performance metrics to be used at all levels of the organization (site, division and corporate), collaborating with process owners and key stakeholders in corporate, division and site. Ensure NC and CAPA metrics are appropriately cascaded through Management Reviews.
  • Work closely with NC and CAPA owners to ensure timelines are met with high quality documentation.
  • Standardize alert and action limits for escalations to senior leaders and other stakeholders
  • Ensure key process indicators of NCs and CAPAs are integrated into Quality Management Reviews.
  • Evaluate new regulations, guidelines and industry standards and their impact on CAPA and NC activities; plan and effectively implement plans across the business to maintain compliance.
  • All other duties and responsibilities as assigned

DESIRED MINIMUM QUALIFICATIONS
The requirements listed below are representative of the knowledge, skill and/or ability required for his position.
Education:
  • Bachelor's degree is required, preferably in a scientific or engineering discipline.
  • 10+ years of demonstrated quality experience in the medical product and device industry with strong concentration in US FDA QMSR and ISO 13485 compliance and quality assurance.
  • Proficient understanding and demonstrated practical application of medical device regulations which include CAPA, NC and Metrics.

Skills/Knowledge:
  • Experience with communicating with domestic and international regulatory bodies.
  • Strong analytical, strategic, decision making, and risk assessment abilities.
  • Ability to effectively collaborate with process owners and stakeholders in corporate, division and site
  • Highly developed technical writing and editing skills.
  • Excellent organizational, leadership, and interpersonal skills.
  • Proficient in the following computer software applications: Microsoft Office, Copilot
  • Exceptional interpersonal skills.
  • Strong organizational and communication skills (written and verbal).
  • Ability to travel domestically and internationally as business required.
  • Experience in FDA regulated environment.
  • Ability to interface with technical and non-technical personnel.
  • Ability to utilize a computer, telephone, smart phone as well as other general office equipment. Strong computer skills are required.

Salary Pay Range:
$125,350.00 - $172,500.00 USD Salary
Our salary ranges are determined by role, level, and location. Individual pay is determined by several factors including job-related skills, experience, and relevant education or trainingIn addition to base pay, employees may be eligible for bonus, commission, equity or other variable compensationYour recruiter can share more about the specific salary range for your preferred location during the hiring process.
Additional Description for Pay Transparency:
Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance, and savings plan (401(k)).
Subject to the terms of their respective policies and date of hire, Employees are eligible for the following https://jobs.integralife.com/total-rewards/
Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status.
This site is governed solely by applicable U.S. laws and governmental regulations. If you'd like more information on your rights under the law, please see the following notices:
EEO Is the Law | EOE including Disability/Protected Veterans
Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA. If you have difficulty using our online system due to a disability and need an accommodation, please email us at careers@integralife.com.
Unsolicited Agency Submission
Integra LifeSciences does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. A formal written agreement is required before engaging any agency, and it must be executed and authorized by the Vice President, Talent Acquisition. Where agency agreements are in place, introductions (the initial sharing of a candidate's name, resume, or background) are position-specific and may only occur within the scope of that approved agreement. Please, no phone calls or emails.
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