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Capa Jobs in Atlanta, GA (NOW HIRING)

Chubb

StreamLabs - QA Manager

Smyrna, GA · On-site

Support corrective and preventive action (CAPA) activities * Collaborate with cross-functional teams (engineering, production, supply chain, etc.) to resolve quality concerns * Prepare and maintain ...

Chubb

StreamLabs - QA Manager

Smyrna, GA · On-site

Support corrective and preventive action (CAPA) activities * Collaborate with cross-functional teams (engineering, production, supply chain, etc.) to resolve quality concerns * Prepare and maintain ...

Carlyle's Catering

Be Seen First

Quality Assurance (QA) Manager / Food Safety Manager

Atlanta, GA · On-site

$55K - $65K/yr

CAPA Reports * Internal Audits Continuous Improvement * Analyze quality trends. * Reduce food waste. * Improve product consistency. * Improve audit scores. * Reduce customer complaints. * Improve ...

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Showing results 21-40

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See Atlanta, GA salary details

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$41

$69

How much do capa jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for capa in Atlanta, GA is $41.75, according to ZipRecruiter salary data. Most workers in this role earn between $31.65 and $48.55 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?

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 Atlanta, GA? The most popular types of Capa jobs in Atlanta, GA are:
What are popular job titles related to Capa jobs in Atlanta, GA? For Capa jobs in Atlanta, GA, the most frequently searched job titles are:
What job categories do people searching Capa jobs in Atlanta, GA look for? The top searched job categories for Capa jobs in Atlanta, GA are:
Capa jobs near you
Infographic showing various Capa job openings in Atlanta, GA as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $86,832 per year, or $41.7 per hour.

Sr. Manager, Quality Systems & Compliance

Werfen

Norcross, GA • On-site

Full-time

Re-posted 13 days ago

Werfen rating

8.7

Company rating: 8.7 out of 10

Based on 27 frontline employees who took The Breakroom Quiz

Job description

Introduction
Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.
Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We're passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care.
Overview
Job Summary
  • Responsible for leading and maintaining the Quality Systems & Compliance function for the Norcross Transfusion site. Provides strategic and operational leadership for the Quality Management System (QMS), ensuring sustainable compliance with applicable FDA Quality System Regulation (QMSR), ISO 13485, IVDR, MDSAP, and other global regulatory requirements.
  • Accountable for Quality Systems governance, document control, training compliance, internal audits, supplier quality oversight, CAPA governance, management review, inspection readiness, quality met-rics, and continuous improvement programs.

Responsibilities
Key Accountabilities
  • Own and maintain the site Quality Management System (QMS).
  • Lead Document Control, Internal Audit, Inspection Readiness, and Management Review programs.
  • Provide governance of Deviations, Nonconformances, CAPA, Change Control, and Risk Management.
  • Lead Supplier Quality governance and supplier audit activities.
  • Develop and report quality metrics and compliance indicators.
  • Drive continuous improvement initiatives utilizing Lean and Six Sigma methodologies.
  • Lead and develop a high-performing Quality Systems & Compliance team by fostering engagement, accountability, collaboration, and continuous professional development to achieve quality, compli-ance, and business objectives.
  • Partner cross-functionally to ensure lifecycle quality integration.

Networking/Key relationships
The purpose of the interactions with the listed departments is to promote quality Quality System, Compliance, and Inspection Readiness. This role interacts with the following departments:
  • Manufacturing Operations
  • Manufacturing Technical Support
  • Laboratory Services
  • Design & Sustaining Quality
  • Regulatory Affairs
  • Post-Market Surveillance
  • Supply Chain
  • Engineering

Qualifications
Minimum Knowledge & Experience required for the position:
  • Bachelor's degree in Engineering, Life Sciences, Quality, Regulatory Affairs, Business, or related discipline.
  • 8+ years (Manager) or 10+ years (Sr. Manager) in Quality Systems, Compliance, QA, or Regulatory Affairs within a regulated environment.
  • Leadership experience required

Management has the discretion of substituting relevant work experience for a degree and/or making exceptions to the years of experience requirement.
Skills & Capabilities:
  • Expert knowledge of FDA QMSR, ISO 13485, IVDR, MDSAP, auditing, CAPA, and quality systems.
  • Strong leadership, coaching, communication, and project management skills.
  • Experience leading inspections and external audits.

Travel requirements:
Travel is required less than 10% of the time.
Closing
If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV.
Werfen is an Equal Opportunity employer and is committed to a diverse workplace. Werfen strictly prohibits unlawful discrimination, harassment or retaliation based upon an individual's race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other protected characteristic as defined by applicable state or federal law. If you have a disability and need an accommodation in relation to the online application process, please contact NAtalentacquisition@werfen.com for assistance.
We operate directly in over 30 countries, and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 7,000 employees around the world comprise our Werfen team.
www.werfen.com

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About Werfen

Sourced by ZipRecruiter

Industry

Health care and social assistance

Company size

1,001 - 5,000 Employees

Headquarters location

L'Hospitalet de Llobregat, Barcelona, ES

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