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Assistant Quality Control Manager Jobs in Georgia

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 ...

Work closely with project managers, engineers, and subcontractors to coordinate quality control activities and resolve quality-related issues. * Maintain effective communication with clients and ...

Ryan Companies US, Inc. has an immediate career opportunity for a Quality Control Manager to join our national Mission Critical sector team! Do you bring at last 5 years of successful field quality ...

Ryan Companies US, Inc. has an immediate career opportunity for a Quality Control Manager to join our national Mission Critical sector team! Do you bring at last 5 years of successful field quality ...

Manager, Quality Control We are looking for a Quality Control Manager to join our Peachtree City, GA team! The Quality Manager for our facility oversees the testing, validation, and process control ...

Ryan Companies US, Inc. has an immediate career opportunity for a Quality Control Manager to join our national Mission Critical sector team! Do you bring at last 5 years of successful field quality ...

Manager, Quality Control We are looking for a Quality Control Manager to join our Peachtree City, GA team! The Quality Manager for our facility oversees the testing, validation, and process control ...

SSHO/QC

Savannah, GA · On-site

$77K - $103K/yr

The SSHO/QC Manager position will develop and implement the quality/safety program, QC/Safety plans, enforcing policies, assessing risk, and ensuring compliance with legal guidelines for the Mountain ...

QA/QC Assistant

Atlanta, GA · On-site

$18 - $19/hr

ISO 9001 and/or Quality Management System (QMS) experience is a plus. The QA/QC Assistant supports the QA/QC Manager in maintaining and improving quality assurance processes, policies, and procedures ...

Showing results 21-40

Assistant Quality Control Manager information

See Georgia salary details

$9

$19

$34

How much do assistant quality control manager jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for assistant quality control manager in Georgia is $19.28, according to ZipRecruiter salary data. Most workers in this role earn between $13.80 and $19.47 per hour, depending on experience, location, and employer.

What does an assistant quality control manager do?

An Assistant Quality Control Manager supports the Quality Control Manager in overseeing product quality and ensuring that manufacturing processes comply with company standards and regulatory requirements. They supervise quality control staff, assist in developing and implementing testing procedures, and analyze data to identify areas for improvement. Their role is crucial for maintaining product consistency, safety, and customer satisfaction, while also working to resolve any issues that may arise during production.

What are the key skills and qualifications needed to thrive as an assistant quality control manager?

To thrive as an Assistant Quality Control Manager, you need a solid understanding of quality assurance processes, statistical analysis, and industry-specific regulations, usually supported by a relevant bachelor's degree. Familiarity with quality management systems (QMS), inspection tools, and certifications such as Six Sigma or ISO 9001 is often expected. Strong attention to detail, leadership, and effective communication skills help foster team collaboration and drive process improvements. These competencies ensure consistent product quality, compliance, and operational efficiency within the organization.

What are some common challenges faced by an assistant quality control manager, and how can they be addressed?

Assistant Quality Control Managers often encounter challenges such as maintaining consistent quality standards across multiple shifts, managing tight production schedules, and ensuring compliance with changing regulations. Effective communication with both production staff and senior management is crucial for promptly addressing quality issues. Staying proactive by implementing regular training sessions and fostering a culture of continuous improvement can help mitigate these challenges and ensure smooth operations within the quality control team.

What is the difference between Assistant Quality Control Manager vs Quality Control Technician?

AspectAssistant Quality Control ManagerQuality Control Technician
CredentialsTypically requires a bachelor's degree in quality assurance, engineering, or related field; certifications like ASQ CQE are commonUsually holds a high school diploma or associate degree; certifications like ASQ CQPA may be preferred
Work EnvironmentWorks in office and lab settings, overseeing quality processes and team coordinationPrimarily lab or production floor, performing testing and inspections
Employer & Industry UsageUsed in manufacturing, pharmaceuticals, and food industries for supervisory rolesCommon in manufacturing and production plants for technical testing roles

The Assistant Quality Control Manager focuses on supervising quality assurance processes and managing teams, requiring more advanced education and certifications. In contrast, the Quality Control Technician performs hands-on testing and inspections, often with less formal education. Both roles are essential in maintaining product quality but differ in responsibilities and level of oversight.

What cities in Georgia are hiring for Assistant Quality Control Manager jobs?

Cities in Georgia with the most Assistant Quality Control Manager job openings:

Infographic showing various Assistant Quality Control Manager job openings in Georgia as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 13% Part Time, 8% Contract, and 3% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $40,108 per year, or $19.3 per hour.

Quality Control Manager

AstraZeneca

Bogart, GA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 18 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.

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About AstraZeneca

Sourced by ZipRecruiter

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.

Industry

Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Cambridge, Cambridgeshire, GB