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Capa Manager Jobs in Georgia (NOW HIRING)

Process Engineer

Norcross, GA · On-site

$75K - $90K/yr

Proven ability in CAPA management and root cause analysis facilitation. * Working knowledge of ERP systems (preferably Odoo). * Ability to influence cross-functional teams and drive quality-focused ...

Proven ability in CAPA management and root cause analysis facilitation. * Working knowledge of ERP systems (preferably Odoo). * Ability to influence cross-functional teams and drive quality-focused ...

The Quality Manager will play a key leadership role in driving product quality, food safety, and ... Why, CAPA, A3, SPC, Lean Six Sigma, and FMEA. * Partner cross-functionally with Operations ...

Be Seen First

CAPA Reports * Internal Audits Continuous Improvement * Analyze quality trends. * Reduce food waste ... HACCP Management* Food Safety Leadership Preferred: * Commissary Operations * Wholesale ...

Support corrective and preventive action (CAPA) activities * Collaborate with cross-functional ... Support supplier quality management and conduct supplier audits or inspections * Participate in ...

Corrective Action / Preventative Action (CAPA) * Safety practices * PHI / PI (Confidentiality) * Provide direction and management oversight for QMS activities including (but not limited to)

Support corrective and preventive action (CAPA) activities * Collaborate with cross-functional ... Support supplier quality management and conduct supplier audits or inspections * Participate in ...

Support execution of CAPA, audit responses, and inventory-related escalations. People Leadership Directly manage and develop ICQA Leads and Associates. Create a culture of accuracy, accountability ...

Support execution of CAPA, audit responses, and inventory-related escalations. People Leadership Directly manage and develop ICQA Leads and Associates. Create a culture of accuracy, accountability ...

Stord manages over $10 billion of commerce annually through its fulfillment, warehousing ... Support execution of CAPA, audit responses, and inventory-related escalations. * Maintain proper ...

Stord manages over $10 billion of commerce annually through its fulfillment, warehousing ... Support execution of CAPA, audit responses, and inventory-related escalations. * Maintain proper ...

Showing results 21-40

Capa Manager information

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 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 popular job titles related to Capa Manager jobs in Georgia? For Capa Manager jobs in Georgia, the most frequently searched job titles are:
What job categories do people searching Capa Manager jobs in Georgia look for? The top searched job categories for Capa Manager jobs in Georgia are:
What cities in Georgia are hiring for Capa Manager jobs? Cities in Georgia with the most Capa Manager job openings:
Infographic showing various Capa Manager job openings in Georgia as of August 2026, with employment types broken down into 90% Full Time, 9% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution.

Sr. Manager, Quality Systems & Compliance

Werfen

Norcross, GA • On-site

Full-time

Re-posted 11 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

Employment Type: FULL_TIME

What Werfen employees say

Pay

Benefits

Hours and flexibility

Workplace

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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