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Biotech Quality Control Jobs in Georgia (NOW HIRING)

Alexion Pharmaceuticals

Quality Control Manager

Bogart, GA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Microbiology experience in quality control within a biotech , pharmaceutical , or biopharmaceutical manufacturing environment is helpful. * Prior supervisory experience is preferred. Competencies

Alexion Pharmaceuticals

Quality Control Manager

Bogart, GA

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Microbiology experience in quality control within a biotech , pharmaceutical , or biopharmaceutical manufacturing environment is helpful. * Prior supervisory experience is preferred. Competencies

AstraZeneca

Quality Control Manager

Bogart, GA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Microbiology experience in quality control within a biotech , pharmaceutical , or biopharmaceutical manufacturing environment is helpful. * Prior supervisory experience is preferred. Competencies

Kelly Services

QC Laboratory Technician

Conley, GA

$26.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Previous laboratory experience is required , preferably in QC, pharmaceutical, biotechnology, or manufacturing environments. * Working knowledge of FDA, GLP, and GMP requirements. * Experience with ...

CorDx

Quality Coordinator

Atlanta, GA

  • Medical

  • Retirement

  • PTO

... control measures, monitor performance of our products, and identify opportunities for improvement. The successful candidate will have a strong background in quality assurance in the biotechnology ...

CorDx

Quality Coordinator

Atlanta, GA · On-site

  • Medical

  • Retirement

  • PTO

... control measures, monitor performance of our products, and identify opportunities for improvement. The successful candidate will have a strong background in quality assurance in the biotechnology ...

CorDx

Quality Coordinator

Atlanta, GA · On-site

  • Medical

  • Retirement

  • PTO

... control measures, monitor performance of our products, and identify opportunities for improvement. The successful candidate will have a strong background in quality assurance in the biotechnology ...

GTT, LLC

Quality Control Technician - DHR

Atlanta, GA · On-site

$28.06/hr

  • Medical

  • Dental

  • Vision

  • Retirement

Quality Control Technician - DHR Location: Atlanta, GA Onsite Flexibility: Onsite Contract Details ... biotech, utilities, and retail sectors throughout the U.S. and Canada. Job Number: 26-11493 ...

New

Manus Bio

Quality Technician

Augusta, GA · On-site

$17 - $22.75/hr

... biotechnology today. Manus is seeking a detail-oriented Quality Technician (Contractor) to support day-to-day quality control (QC) testing and quality assurance (QA) plant audit activities at our ...

Manus Bio

Quality Technician

Augusta, GA · On-site

$14.25 - $19/hr

... biotechnology today. Manus is seeking a detail-oriented Quality Technician (Contractor) to support day-to-day quality control (QC) testing and quality assurance (QA) plant audit activities at our ...

Manus

Quality Technician

Augusta, GA · On-site

$14.25 - $19/hr

... biotechnology today. Manus is seeking a detail-oriented Quality Technician (Contractor) to support day-to-day quality control (QC) testing and quality assurance (QA) plant audit activities at our ...

CorDx

Quality Assurance Manager

Alpharetta, GA

  • Medical

  • Retirement

  • PTO

Who is CorDx CorDx a multi-national biotech organization focused on pushing the limits of ... Proficiency in QMS software and documentation control systems . * Strong analytical and problem ...

CorDx

Quality Assurance Manager

Chamblee, GA

  • Medical

  • Retirement

  • PTO

Who is CorDx CorDx a multi-national biotech organization focused on pushing the limits of ... Proficiency in QMS software and documentation control systems . * Strong analytical and problem ...

CorDx

Quality Assurance Manager

Alpharetta, GA · On-site

  • Medical

  • Retirement

  • PTO

Who is CorDx? CorDx a multi-national biotech organization focused on pushing the limits of ... Proficiency in QMS software and documentation control systems . * Strong analytical and problem ...

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All JobsBiotech Quality Control JobsBiotech Quality Control Jobs in Georgia

Biotech Quality Control information

See Georgia salary details

$25.8K

$68.7K

$109.3K

How much do biotech quality control jobs pay per year?

As of Aug 17, 2026, the average yearly pay for biotech quality control in Georgia is $68,668.00, according to ZipRecruiter salary data. Most workers in this role earn between $51,100.00 and $84,400.00 per year, depending on experience, location, and employer.

What is a biotech quality control?

A Biotech Quality Control (QC) job involves ensuring that biological products, processes, and facilities meet regulatory and quality standards. QC professionals conduct testing, analyze data, and document results to verify product safety and efficacy. They work with laboratory techniques such as PCR, HPLC, and microbiological testing. The role is critical in maintaining compliance with industry regulations like GMP and FDA guidelines.

What does a biotech quality control do?

On a daily basis, a Biotech Quality Control professional performs routine testing and analysis of raw materials, intermediates, and finished products to ensure they meet established specifications. This involves preparing samples, operating analytical equipment, maintaining accurate records, and documenting results in compliance with regulatory guidelines. Quality Control staff also collaborate closely with production, quality assurance, and research teams to troubleshoot issues and support process improvements. Regular internal audits and participation in team meetings are common, making communication and teamwork key parts of the job.

What are the key skills and qualifications needed to thrive in biotech quality control?

To excel in Biotech Quality Control, candidates typically need a background in biology, chemistry, or related sciences, with strong knowledge of laboratory techniques and regulatory requirements. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and common analytical instruments such as HPLC or PCR is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for this role. These competencies are vital for ensuring that biotech products consistently meet quality and compliance standards essential for patient safety and regulatory approval.

What are the most commonly searched types of Biotech Quality Control jobs in Georgia?

The most popular types of Biotech Quality Control jobs in Georgia are:

What are popular job titles related to Biotech Quality Control jobs in Georgia?

For Biotech Quality Control jobs in Georgia, the most frequently searched job titles are:

What job categories do people searching Biotech Quality Control jobs in Georgia look for?

The top searched job categories for Biotech Quality Control jobs in Georgia are:

What cities in Georgia are hiring for Biotech Quality Control jobs?

Cities in Georgia with the most Biotech Quality Control job openings:

Biotech Quality Control jobs near you
Infographic showing various Biotech Quality Control job openings in Georgia as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $68,668 per year, or $33 per hour.

Quality Control Manager

Alexion Pharmaceuticals

Bogart, GA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 14 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.

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