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Quality Control Lab Manager Jobs in Gainesville, GA

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 ...

A 4-year degree in chemistry or related field, Masters Preferred, and 3-4 years of experience in a Quality Control Lab or similar chemistry field. Familiarity with analytical testing concepts ...

Bogart, GA 100% onsite Work type: 100% lab based role Contract duration: 12 months Pay Range: $30 ... Recognizes aberrant test and sample conditions and reports them to the area supervisor / manager ...

... Management System (LIMS). The standard shift is 8:00am-4:30pm, but may occasionally require 2nd ... AGW delivers operational, clinical, lab and professional talent with a strong focus on healthcare ...

Quality Control Technician

Demorest, GA · On-site

$16.25 - $20.75/hr

The Quality Control Technician position entails the testing and inspection of Hot Mix Asphalt (HMA ... management skills are needed. High degree of safety awareness and safety discipline Display a ...

Quality Control Technician

Demorest, GA · On-site

$16.25 - $20.75/hr

The Quality Control Technician position entails the testing and inspection of Hot Mix Asphalt (HMA ... time management skills are needed. • High degree of safety awareness and safety discipline • ...

Uses advanced inspection methods to develop and conduct quality programs. * Works under general ... management systems Work Environment and Physical Requirements: Activity Constantly - 6+ hours

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Quality Control Lab Manager information

See Gainesville, GA salary details

$28.4K

$75.8K

$120.8K

How much do quality control lab manager jobs pay per year?

As of Aug 15, 2026, the average yearly pay for quality control lab manager in Gainesville, GA is $75,830.00, according to ZipRecruiter salary data. Most workers in this role earn between $56,400.00 and $93,200.00 per year, depending on experience, location, and employer.

What does a quality control lab manager do?

A Quality Control Lab Manager oversees the daily operations of a laboratory to ensure that products meet industry and safety standards. They supervise lab staff, develop testing protocols, review test results, and maintain compliance with regulatory guidelines. The manager is also responsible for training employees, troubleshooting equipment, and implementing improvements to lab processes. Their work is crucial in guaranteeing the quality and safety of products before they reach consumers.

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

AspectQuality Control Lab ManagerQuality Control Technician
CredentialsBachelor's degree in science or related field; often certifications in quality managementAssociate's or bachelor's degree; relevant technical certifications
Work EnvironmentLaboratories, overseeing testing processes and staffLaboratories, performing tests and data collection
ResponsibilitiesSupervising testing activities, managing staff, ensuring complianceConducting tests, recording results, maintaining equipment

The main difference between a Quality Control Lab Manager and a Quality Control Technician lies in their responsibilities and level of oversight. The manager oversees testing operations, manages staff, and ensures quality standards, while the technician performs the actual testing and data collection. Both roles require relevant scientific credentials and work in laboratory environments, but the manager holds a broader supervisory role.

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

Quality Control Lab Managers often face challenges such as ensuring compliance with evolving regulatory standards, maintaining the accuracy and reliability of test results, and managing a diverse team of technicians. To address these issues, managers must stay updated on industry regulations, implement rigorous training programs, and foster open communication within the team. Effective use of laboratory information management systems (LIMS) and regular audits can also help maintain high-quality standards and streamline workflows.

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

To thrive as a Quality Control Lab Manager, you need a solid background in chemistry or biology, experience in laboratory operations, and often a relevant degree or certification. Familiarity with laboratory information management systems (LIMS), analytical instrumentation, and quality standards such as ISO or GMP is typically required. Strong leadership, attention to detail, and effective communication are vital soft skills for managing teams and ensuring compliance. These skills and qualities are crucial to maintain product quality, regulatory adherence, and efficient laboratory performance.

What are popular job titles related to Quality Control Lab Manager jobs in Gainesville, GA?

For Quality Control Lab Manager jobs in Gainesville, GA, the most frequently searched job titles are:

What job categories do people searching Quality Control Lab Manager jobs in Gainesville, GA look for?

The top searched job categories for Quality Control Lab Manager jobs in Gainesville, GA are:

What cities near Gainesville, GA are hiring for Quality Control Lab Manager jobs?

Cities near Gainesville, GA with the most Quality Control Lab Manager job openings:

Quality Control Manager

Alexion Pharmaceuticals

Bogart, GA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 12 days ago


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.