1

Quality Control Auditor Jobs in Georgia (NOW HIRING)

Auditing experience . * Experience representing a functional area on network or cross-functional ... Microbiology experience in quality control within a biotech , pharmaceutical , or biopharmaceutical ...

QA/QC Assistant

Atlanta, GA · On-site

$18 - $19/hr

Minimum of two years of relevant work experience in quality assurance, auditing, compliance, data ... The QA/QC Assistant supports the QA/QC Manager in maintaining and improving quality assurance ...

Quality Control Technician

Atlanta, GA · On-site

$18 - $23/hr

Job Title: Quality Control Technician Location: Atlanta, GA 30313 Duration: 12 Months Work ... Internal Auditing * Attention to Detail * Documentation & Record Management Computer Skills

$24 - $27/hr

The Quality Assurance Auditor will analyze, document, and report on results to business ... Three (3) years of experience in quality assurance/quality control, compliance monitoring ...

The Quality Control Electrician is responsible for delivery of quality control services including coordination and implementation of the Quality Control Plan, job site Quality auditing, conducting on ...

The Quality Control Electrician is responsible for delivery of quality control services including coordination and implementation of the Quality Control Plan, job site Quality auditing, conducting on ...

The Quality Control Electrician is responsible for delivery of quality control services including coordination and implementation of the Quality Control Plan, job site Quality auditing, conducting on ...

The Quality Control Electrician is responsible for delivery of quality control services including coordination and implementation of the Quality Control Plan, job site Quality auditing, conducting on ...

Quality Auditor Job Location: Stone Mountain, GA Reports To: Safety & Quality Supervisor Job ... Assists and audits production lines in accordance with established Quality Control Procedures and ...

The Quality Auditor provides technical guidance to the Quality Assurance team, within a business ... Maintains and tracks quality for the purposes of analysis, control, and management reports

The Quality Auditor provides technical guidance to the Quality Assurance team, within a business ... Maintains and tracks quality for the purposes of analysis, control, and management reports

The Quality Auditor provides technical guidance to the Quality Assurance team, within a business ... Maintains and tracks quality for the purposes of analysis, control, and management reports

Showing results 21-40

Quality Control Auditor information

See Georgia salary details

$8

$21

$38

How much do quality control auditor jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for quality control auditor in Georgia is $21.35, according to ZipRecruiter salary data. Most workers in this role earn between $15.24 and $25.58 per hour, depending on experience, location, and employer.

What is quality control auditing?

Quality control auditing involves systematically reviewing and evaluating a company's processes and products to ensure they meet specified standards and quality requirements. For a Quality Control Auditor, this includes inspecting materials, documenting findings, and verifying compliance using checklists or testing tools to maintain product quality and safety.

How does a quality control auditor typically interact with production and management teams during the audit process?

Quality Control Auditors regularly collaborate with both production staff and management to ensure products meet company and regulatory standards. During audits, they communicate findings and potential areas for improvement to production teams, providing actionable feedback. They also report major issues or trends to management, helping to drive process improvements and uphold compliance. Effective communication and diplomacy are essential, as auditors often need to balance enforcing standards with fostering a positive team environment.

What is the difference between Quality Control Auditor vs Quality Inspector?

AspectQuality Control AuditorQuality Inspector
Primary RoleReview and analyze quality processes, audit compliance, identify systemic issuesInspect products or materials for defects, ensure quality standards are met
CertificationsISO auditor, Six Sigma, quality management certificationsQuality inspection certifications, OSHA safety training
Work EnvironmentOffice settings, manufacturing plants, warehousesManufacturing lines, warehouses, labs
Employer & IndustryManufacturing, aerospace, automotive, food productionManufacturing, electronics, consumer goods

While both roles focus on quality, a Quality Control Auditor evaluates overall processes and compliance through audits, whereas a Quality Inspector performs hands-on inspections of products to detect defects. The auditor's work is more analytical and process-oriented, while the inspector's role is more product-focused.

What are the key skills and qualifications needed to thrive as a quality control auditor, and why are they important?

To thrive as a Quality Control Auditor, you need a solid understanding of quality assurance standards, attention to detail, and a background in fields such as manufacturing, pharmaceuticals, or food safety, often supported by relevant certifications. Familiarity with statistical process control software, audit management systems, and ISO or GMP compliance tools is common in this role. Strong analytical skills, effective communication, and integrity help auditors objectively assess processes and collaborate with teams. These skills ensure that products and services consistently meet regulatory and organizational standards, minimizing errors and maintaining customer trust.

How do I become a quality control auditor?

To become a quality control auditor, typically a high school diploma or equivalent is required, with many employers preferring candidates with a bachelor's degree in quality assurance, manufacturing, or a related field. Relevant skills include attention to detail, knowledge of quality standards and inspection tools, and sometimes certification such as the Certified Quality Auditor (CQA) from the American Society for Quality (ASQ). Experience in manufacturing or production environments can also be beneficial.

What is a quality control auditor?

Quality Control Auditors are professionals responsible for inspecting and evaluating products, processes, or services to ensure they meet established quality standards and regulatory requirements. They review production procedures, conduct tests or inspections, and document their findings to identify areas for improvement. Their work helps organizations maintain consistent product quality, reduce errors, and comply with industry regulations. Quality Control Auditors often work in manufacturing, pharmaceuticals, food production, and other industries where quality assurance is critical.
What are popular job titles related to Quality Control Auditor jobs in Georgia? For Quality Control Auditor jobs in Georgia, the most frequently searched job titles are:
What are popular job titles related to Quality Control Auditor jobs in GA? For Quality Control Auditor jobs in GA, the most frequently searched job titles are:
Infographic showing various Quality Control Auditor job openings in Georgia as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, 1% Temporary, 4% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $44,402 per year, or $21.3 per hour.

Quality Control Manager

AstraZeneca

Bogart, GA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 7 days ago


AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

22nd of 86 rated pharmaceutical


Job description

Position Summary
The person in charge of QC is responsible for leading all Quality Control activities at the Alexion Georgia Manufacturing Facility in Bogart, including oversight of QC operations, personnel, and budget. The role includes responsibility for microbiological and analytical testing of commercial egg white and related materials, genetic testing for Kanuma LAL-C chickens, and facility and utility monitoring, including management of testing performed by contract laboratories where applicable.
This leader will define and complete the site's QC strategic roadmap to strengthen business continuity, risk mitigation, continuous improvement, compliance, and microbial control.
The role is also accountable for ensuring compliance and inspection readiness across all on-site QC activities in accordance with regulatory and quality requirements, including testing to licensed specifications, oversight of contract testing services, and technical support for new registrations.
In addition, the QC Manager will support development and execution of the Global Lab Systems Strategy, including annual goals and objectives, long-range planning, budget planning, people strategy, and laboratory performance management.
Principal Responsibilities
The successful candidate will:
  • Lead QC operations to ensure laboratory activities are compliant, efficient, and safe, while applying testing, Lean, and safety standards.
  • Handle QC laboratory teams supporting in-process testing, microbiological site support, and CLO testing activities.
  • Oversee laboratory scheduling and performance to meet regulatory, quality, and business requirements.
  • Ensure validation and qualification of test methods and instruments supporting in-process and commercial release testing.
  • Maintain inspection readiness and represent QC during audits, inspections, and regulatory interactions.
  • Lead QC risk assessments and ensure timely implementation of mitigation actions.
  • Direct the environmental monitoring program in partnership with Manufacturing to maintain a robust processing and monitoring strategy.
  • Drive analytical method transfers and CLO insourcing to support the QC transgenic roadmap and improve business continuity and risk mitigation.
  • Lead recruitment, retention, development, and performance management of QC staff to build an agile and flexible organization.
  • Oversee the QC training strategy, including development, delivery, evaluation, and retraining programs as needed.
  • Ensure effective quality control assistance for investigations, including laboratory investigation reports, deviations, and CAPAs, in compliance with Alexion procedures and timelines. Including the completion of LIR and EM trend reports.
  • Lead tiered communication and task prioritization within QC to support commercial operations.
  • Ensure timely completion of testing and data review/approval to support batch disposition.
  • Provide QC support for the APQR process and process monitoring activities.
  • Build continuous improvement capability within QC and apply CI tools to drive performance improvements, with focus on new technologies and appropriate use of AI.

Qualifications
  • Minimum 10 years of experience in a GMP laboratory.
  • Demonstrated ability to build, mentor, and develop high-performing teams.
  • Shown success working in a matrix organization.
  • Comprehensive knowledge of current regulatory requirements related to stability, raw materials, and QC operations in regulated environments.
  • Demonstrated people leadership and experience handling cross-functional teams.
  • Consistent record of implementing Lean laboratory practices, including 5S, visual management, and paperless lab approaches.
  • Strong project management capability.
  • Auditing experience.
  • Experience representing a functional area on network or cross-functional teams.
  • Experience resolving technical issues in a multidisciplinary environment.

Education
  • Candidates must have completed a Bachelor's degree or have comparable experience in biological sciences, chemical sciences, business, or a similar technical field. Experience equivalent to a Bachelor's degree or relevant experience in a regulated industry will also be considered.
  • Microbiology experience in quality control within a biotech, pharmaceutical, or biopharmaceutical manufacturing environment is helpful.
  • Prior supervisory experience is preferred.

Competencies
  • Advanced understanding of the laboratory environment and laboratory techniques used in the analysis of biological drug products.
  • Strong organizational, collaboration, and communication skills.
  • Ability to communicate effectively with senior management and cross-functional collaborators.
  • Strong understanding of cGMP operations, testing concepts, and supporting quality systems.
  • Ability to work effectively across functions, levels, and teams.

The annual base pay for this position ranges from $ 112,604.80 - 168,907.20. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
04-Aug-2026
Closing Date
31-Aug-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

What AstraZeneca employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom