1

Quality Systems Manager Jobs in Georgia (NOW HIRING)

Quality Management Essential Functions: * Serve as Lead Auditor & Trainer for the Quality Management System. * Oversee the maintenance of and adherence to industry, customer, and internal standards.

Quality Management Essential Functions: * Serve as Lead Auditor & Trainer for the Quality Management System. * Oversee the maintenance of and adherence to industry, customer, and internal standards.

The right person for this role has extensive knowledge in Quality Management System (QMS) systems, data analysis, and continuous improvement to help shape our internal systems, tools, procedures and ...

Quality Control Systems Manager Location: Ft. Benning- Columbus, GA Division: Potawatomi Defense Operations ** Position contingent upon contract award Position Summary: This position will provide the ...

The Quality Systems Analyst reports to the Quality Manager. The Quality Systems Analyst must conduct themselves in a professional manner. Apply company policies and procedures to resolve a variety of ...

New

The Quality Systems Analyst reports to the Quality Manager. The Quality Systems Analyst must conduct themselves in a professional manner. Apply company policies and procedures to resolve a variety of ...

New

Manage customer and vendor return processes, while serving as a key point of contact for customer ... Quality Management System (QMS). * Perform internal quality audits and support external audits ...

Showing results 21-40

Quality Systems Manager information

See Georgia salary details

$45.6K

$83.3K

$130K

How much do quality systems manager jobs pay per year?

As of Aug 9, 2026, the average yearly pay for quality systems manager in Georgia is $83,267.00, according to ZipRecruiter salary data. Most workers in this role earn between $63,800.00 and $103,400.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a quality systems manager?

To thrive as a Quality Systems Manager, you need strong expertise in quality management principles, regulatory compliance, and process improvement, typically supported by a degree in engineering or a related field. Familiarity with ISO standards (like ISO 9001), quality management software, and certifications such as Six Sigma or ASQ Certified Manager of Quality/Organizational Excellence are commonly required. Leadership, analytical thinking, and effective communication are crucial soft skills for coordinating teams and driving continuous improvement. These skills and qualifications are essential to ensure consistent product quality, regulatory adherence, and overall organizational efficiency.

What is the difference between Quality Systems Manager vs Quality Assurance Manager?

AspectQuality Systems ManagerQuality Assurance Manager
Primary FocusDeveloping and maintaining quality management systems and processesOverseeing product testing and ensuring quality standards are met during production
CertificationsISO 9001 Lead Auditor, CQEASQ certifications, QA certifications
Work EnvironmentQuality management departments, compliance teamsProduction lines, testing labs
Industry UsageManufacturing, healthcare, aerospaceManufacturing, software, healthcare

While both roles focus on quality, the Quality Systems Manager primarily manages the overall quality management system and compliance, whereas the Quality Assurance Manager concentrates on product testing and ensuring quality during production. Understanding these differences helps in selecting the right career path or hiring the appropriate professional.

What does a quality systems manager do?

As a quality systems manager, your primary responsibilities are monitoring the production processes and ensuring factory machinery/goods are within company and industry requirements. Your duties include weighing, sampling, or testing products for quality and functionality. You may also report the results of quality control tests. You monitor the equipment and people involved, and help with the development and implementation of improved management systems. You are also in charge of creating a standard operating procedure for the specific plant where you work. You check that everything is running at full efficiency and the quality of merchandise is standardized.

How does a quality systems manager typically collaborate with cross-functional teams to drive continuous improvement?

A Quality Systems Manager works closely with departments such as manufacturing, engineering, regulatory, and supply chain to ensure that quality standards are consistently met and improved. They often lead or participate in cross-functional meetings to identify process gaps, analyze data, and develop corrective and preventive action plans. Effective communication and project management skills are essential, as the role involves aligning diverse teams toward common quality objectives and facilitating training or audits to support compliance and improvement initiatives.
What are popular job titles related to Quality Systems Manager jobs in Georgia? For Quality Systems Manager jobs in Georgia, the most frequently searched job titles are:
What cities in Georgia are hiring for Quality Systems Manager jobs? Cities in Georgia with the most Quality Systems Manager job openings:
Infographic showing various Quality Systems Manager job openings in Georgia as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $83,267 per year, or $40 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

What Werfen employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


Werfen logo

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