Laboratory Manager Jobs in Georgia
Laboratory Manager jobs in Georgia are in strong demand, concentrated in clinical diagnostics, pharmaceutical manufacturing, and research, with openings at every level from bench supervisor to senior laboratory director. Atlanta, Augusta, and Savannah lead hiring activity, anchored by employers such as Emory Healthcare, Piedmont Healthcare, and Gulfstream Aerospace, which maintain significant laboratory operations across the state. Quality control, clinical chemistry, and environmental testing are the specialties drawing the most consistent interest from Georgia employers. Find a role that fits below and apply directly.
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Job Title
Quality Systems & Laboratory Manager
Job Summary
The Quality Manager leads the Quality Management Systems, laboratory operations, testing programs, and incoming product quality functions for the Locust Grove and Wood Dale facilities. As the site quality leader, this position has primary responsibility for the effectiveness, compliance, and continual improvement of the QMS and for maintaining ISO 9001 certification while ensuring customer, regulatory, statutory, and organizational requirements are effectively translated into operational controls.
The position provides leadership and technical oversight for incoming inspection, laboratory and product testing, calibration and measurement systems, test method validation, inspection planning, quality documentation, and certification activities. Working cross-functionally with Corporate Quality, Operations, Engineering, Supply Chain, and Procurement, and directly with suppliers when required, the Quality Engineering Manager ensures appropriate controls are established throughout the receipt, inspection, testing, acceptance, and distribution of product.
The Quality Manager establishes and strengthens the procedures, work instructions, testing protocols, inspection plans, training, and quality controls necessary to support reliable product conformity and operational performance. The role is expected to identify and mitigate quality risks, analyze performance and quality trends, resolve systemic issues, strengthen technical capabilities, and lead continuous improvement initiatives. Equally important, the position develops and reinforces a culture in which quality, compliance, accountability, ethical decision-making, and continuous improvement are integrated into everyday operations
Job Duties
- Lead, develop, maintain, and continually improve the Locust Grove ISO 9001 Quality Management System (QMS), while providing ongoing quality leadership and support for the Wood Dale ISO 9001 QMS to ensure continued certification, compliance, effectiveness, and alignment with organizational requirements.
- Serve as the primary site quality representative and liaison with certification bodies, customers, regulatory agencies, Corporate Quality, and other external parties regarding QMS, product quality, testing, and compliance matters for both sites.
- Develop, implement, maintain, and continually improve quality procedures, work instructions, inspection plans, testing protocols, acceptance criteria, forms, records, and other QMS documentation necessary to ensure effective process and product controls.
- Provide overall leadership and technical oversight of laboratory operations, including testing methodologies, equipment, workflow, staffing, capacity, resource planning, safety, and development of laboratory capabilities.
- Establish, manage, and continually improve incoming inspection and testing programs for products and materials received from domestic and international suppliers, ensuring appropriate verification of conformity prior to acceptance and distribution.
- Develop and maintain risk-based inspection plans, sampling strategies, acceptance criteria, and verification methods based on product requirements, supplier performance, quality history, risk, and applicable customer or technical requirements.
- Lead the administration, technical development, and continual improvement of salt fog, mechanical, dimensional, and other applicable product validation and verification testing programs, ensuring testing is performed consistently and in accordance with defined methods, specifications, standards, and customer requirements.
- Maintain laboratory and testing activities in a state of accreditation readiness, including appropriate control of test methods, equipment, personnel competency, test documentation, reports, records, and supporting objective evidence.
- Lead the site's calibration and metrology program, including measurement standards, equipment qualification, calibration status, traceability, environmental considerations, and controls necessary to ensure the validity and reliability of inspection and test results.
- Establish, validate, and maintain test methods, validation protocols, measurement system controls, and verification techniques to ensure testing and inspection activities produce accurate, repeatable, reproducible, and technically defensible results.
- Ensure effective control, traceability, retention, and accessibility of test reports, certificates of analysis/conformance, product certifications, compliance documentation, calibration records, inspection results, and other quality data and records.
- Coordinate with Corporate Quality to plan and execute the ISO 9001 internal audit program, including audit planning, identification of systemic issues, corrective action follow-up, effectiveness verification, and timely closure of findings.
- Plan, coordinate, and facilitate external certification, surveillance, customer, regulatory, and other third-party audits, ensuring appropriate preparation, response, corrective action, and follow-up.
- Lead the investigation and resolution of product and process nonconformances, inspection or test failures, customer complaints, supplier quality issues, and other quality or compliance concerns, ensuring effective root cause analysis, corrective action, and verification of effectiveness.
- Partner with Operations, Engineering, Supply Chain, Procurement, Corporate Quality, and other facilities to improve product and supplier quality, strengthen process controls, resolve systemic issues, and reduce operational and quality risk.
- Work directly with suppliers, Supply Chain, and Procurement to address supplier performance and product conformity concerns, including corrective actions, improvements to inspection and testing requirements, and verification of sustained improvement.
- Develop, monitor, analyze, and communicate QMS, incoming quality, supplier quality, laboratory, testing, calibration, and audit performance metrics, identifying adverse trends and driving appropriate corrective and improvement actions.
- Develop and maintain appropriate management review inputs, including QMS performance, audit results, customer and supplier performance, nonconformance trends, laboratory performance, risks and opportunities, resource needs, and improvement priorities.
- Provide leadership and oversight of the site's document and record control processes, ensuring procedures, specifications, drawings, standards, engineering documentation, and quality records are appropriately reviewed, approved, controlled, distributed, revised, retained, and protected from unintended use.
- Establish training, qualification, and competency requirements for quality and laboratory personnel and ensure individuals performing inspection, testing, calibration, and other quality-related activities are appropriately trained and competent.
- Provide leadership, coaching, technical guidance, and development for Quality personnel while supporting Operations and other functions in understanding and fulfilling their quality responsibilities.
- Promote a strong quality culture centered on compliance, accountability, ethical behavior, technical discipline, risk-based thinking, customer focus, and continuous improvement.
- Identify and communicate laboratory, metrology, testing, staffing, equipment, and infrastructure needs, and support business justification and capital planning necessary to maintain and expand quality capabilities.
- Support the integration and standardization of quality systems, processes, testing methods, documentation, and best practices between Locust Grove, Wood Dale, Trenton, Corporate Quality, and other facilities where appropriate.
- Travel to the Wood Dale, Illinois facility as required to provide quality management leadership, QMS support, integration, audit support, and continuous improvement, as well as to other company and corporate locations for training, audits, meetings, and other business needs.
- Partner closely with third-party logistics (3PL) providers to investigate and resolve quality nonconformances, customer complaints, product handling concerns, and other quality-related issues, ensuring appropriate corrective actions are implemented and verified for effectiveness.
- Ensure third-party logistics (3PL) operations are appropriately incorporated into the scope and controls of the ISO 9001 Quality Management System, including defined quality requirements, responsibilities, performance monitoring, and adherence to applicable QMS, customer, and product requirements.
Bachelor’s degree in engineering, Quality, or related technical discipline.
Minimum 7–10 years of experience in quality systems, laboratory management, testing, inspection, or manufacturing quality.
Minimum 5 years of leadership experience managing quality systems and technical operations.
Demonstrated experience managing ISO 9001 Quality Management Systems and certification activities and knowledge of ISO 14001.
Experience managing test laboratories, calibration programs, inspection systems, and product testing processes.
Experience supporting incoming quality control, supplier quality, and product verification activities.
Experience with electronic Management Systems (ETQ preferred), calibration management systems, and laboratory data management systems.
Certified ISO 9001 Lead Auditor preferred.
Working knowledge of corrosion testing, environmental testing, salt fog testing, coatings evaluation, or related laboratory validation methods preferred.
Ability to travel approximately 20–30%, primarily to support Quality operations at the Wood Dale, IL facility, with additional travel to other company locations and external events for training, conferences, audits, and other business needs.
Competencies/Skills
- Strong leadership skills with the ability to establish vision, drive accountability, develop teams, and foster a culture of quality, safety, and continuous improvement.
- Ability to influence cross-functional teams and effectively partner with Operations, Supply Chain, Engineering, Procurement, and Corporate Quality leadership.
- Demonstrated success leading quality transformation, compliance initiatives, and organizational change.
- Ability to read and interpret engineering drawings, specifications, and technical requirements, determine appropriate inspection and measurement methods, and select and properly use measurement devices, instruments, and gages.
- Expert knowledge of ISO 9001 requirements, auditing, certification maintenance, and management review processes.
- Experience developing, implementing, and sustaining effective quality and environmental management systems.
- Strong understanding of risk-based thinking, process management, and continuous improvement principles.
- Experience managing laboratory operations, testing programs, test method development, and product validation activities.
- Experience interpreting testing standards, such as ASTM, ANSI, IEC, IEE, etc..
- Understanding of laboratory quality controls, measurement uncertainty, test validation, and data integrity principles.
- Strong knowledge of calibration systems, measurement standards, gauge control, equipment qualification, and metrology principles.
- Ability to ensure traceability, accuracy, and compliance of measurement systems used for inspection and testing.
- Advanced root cause analysis and corrective action skills utilizing 5 Why, Ishikawa, A3, 8D, and risk-based methodologies.
- Proven ability to develop and maintain procedures, work instructions, test methods, inspection plans, specifications, and technical reports.
- Strong document control and records management experience within regulated or certified environments.
Various agencies of the United States Government require employers to maintain information on applicants pertaining to factors such as race, sex, and type of position for which an individual applies. The information requested is voluntary and for compliance with certain record keeping requirements. MacLean Power, LLC has a long-standing commitment to equal employment opportunity for all its associates and applicants for employment. MacLean Power, LLC believes all persons are entitled to equal employment opportunities and does not discriminate against its employees or applicants for employment because of race, color, gender, affectional or sexual orientation, domestic partnership status, ancestry, religion, national origin, citizenship status, marital status, disability, veteran status, age or any other protected group status.
All job offers are conditional, upon successful completion of pre-employment screening, including criminal checks, drug testing, employment, and education verification.
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Where Georgia roles are concentrated, by current openings.
Laboratory Manager Job Market in Georgia
A snapshot from current Georgia openings, updated as new roles post.
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What Georgia Employers Look For
The qualifications that appear most often in laboratory manager jobs across Georgia.
- Bachelor's or master's degree in medical laboratory science, chemistry, biology, or a closely related field
- ASCP Board of Certification or equivalent credential recognized by Georgia employers and clinical partners
- Minimum three to five years of progressively responsible laboratory experience including supervisory duties
- Demonstrated experience managing laboratory accreditation processes such as CAP, CLIA, or ISO standards
- Proficiency with laboratory information systems and quality management software used in Georgia facilities
- Strong regulatory compliance background aligned with Georgia Department of Public Health and federal laboratory standards
Laboratory Manager Jobs in Georgia: Frequently Asked Questions
How do you become a laboratory manager in Georgia?
Most laboratory manager roles in Georgia require a bachelor's degree in medical laboratory science, chemistry, or a related discipline, followed by certification through the ASCP Board of Certification or a comparable credentialing body. Clinical laboratory positions in Georgia are subject to oversight by the Georgia Department of Public Health, which enforces CLIA compliance standards. Candidates typically advance into management after gaining bench experience and completing a supervisory or leadership role within a laboratory setting.
Which companies hire laboratory managers in Georgia?
Employers hiring laboratory managers in Georgia right now include Pratt & Whitney, Emory University, and Quest Diagnostics, based on current listings on Migrate Mate as of November 2026. Georgia's concentration of major hospital systems, contract research organizations, and pharmaceutical manufacturers creates consistent demand for experienced laboratory managers across the state.
Which Georgia cities have the most laboratory manager jobs?
Atlanta, Athens, and Tucker have the most laboratory manager openings in Georgia. Atlanta dominates due to its density of major hospital systems, biotech firms, and corporate headquarters, while Augusta's medical corridor anchors by Wellstar MCG Health and Augusta University drives strong clinical laboratory hiring, and Savannah's industrial and manufacturing base supports quality control and environmental laboratory roles.
Are there remote laboratory manager jobs in Georgia?
Yes, but they're rare. Laboratory manager work is predominantly hands-on and site-dependent, making fully remote positions uncommon in this field. About 50% of laboratory manager openings tied to Georgia are remote or hybrid as of November 2026, and those tend to involve administrative oversight, regulatory compliance review, or multi-site quality management responsibilities that can be handled off-site.
How can I get hired as a laboratory manager in Georgia with little or no experience?
The most realistic entry path is moving into a lead technologist or laboratory supervisor role at a Georgia hospital system or reference laboratory, then building toward management. Emory Healthcare and Piedmont Healthcare both offer structured development pathways for laboratory professionals transitioning into leadership. Earning ASCP certification and gaining experience with CAP or CLIA compliance documentation gives candidates a measurable edge when competing for first-time manager openings.
Where can I find and apply to laboratory manager jobs in Georgia?
You can find and apply to laboratory manager jobs in Georgia on Migrate Mate, which lists current Georgia openings updated regularly. Find roles that match your experience and specialization, then apply directly to the employers posting them.
See All 11 Laboratory Manager Jobs in Georgia
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