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Director Of Risk Control Jobs in Athens, GA (NOW HIRING)

AstraZeneca GmbH

Quality Control Manager

Bogart, GA · On-site

$113 - $169/hr

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 ...

New

AstraZeneca

Quality Control Manager

Bogart, GA · On-site

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 ...

Jj

Exp Anlst Quality Systems

Athens, GA · On-site

... of Risk Management Systems designed to identify, eliminate or reduce, and insure against potential risks to the organization. Assesses and improves quality analysis review process to identify control ...

Johnson & Johnson

Exp Anlst Quality Systems

Athens, GA · On-site

$79 - $128/hr

... of Risk Management Systems designed to identify, eliminate or reduce, and insure against potential risks to the organization. Assesses and improves quality analysis review process to identify control ...

Johnson and Johnson

Exp Anlst Quality Systems

Athens, GA · On-site

... of Risk Management Systems designed to identify, eliminate or reduce, and insure against potential risks to the organization. Assesses and improves quality analysis review process to identify control ...

Johnson & Johnson

Exp Anlst Quality Systems

Athens, GA · On-site

... of Risk Management Systems designed to identify, eliminate or reduce, and insure against potential risks to the organization. Assesses and improves quality analysis review process to identify control ...

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All JobsOf Risk Control JobsDirector Of Risk Control JobsDirector Of Risk Control Jobs in Athens, GA

Director Of Risk Control information

See Athens, GA salary details

$10.6K

$137.1K

How much do director of risk control jobs pay per year?

As of Sep 2, 2026, the average yearly pay for director of risk control in Athens, GA is $136,159.00, according to ZipRecruiter salary data. Most workers in this role earn between $136,100.00 and $136,100.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a director of risk control?

To thrive as a Director Of Risk Control, you need strong expertise in risk management, regulatory compliance, and business operations, often supported by a relevant degree and certifications such as CRM or CPCU. Familiarity with risk assessment software, data analysis tools, and enterprise risk management systems is typically required. Leadership, strategic thinking, and excellent communication skills set outstanding professionals apart in this role. These competencies are critical for effectively identifying, mitigating, and communicating risks to protect organizational assets and ensure regulatory compliance.

How does a director of risk control typically collaborate with other departments to implement effective risk management strategies?

A Director of Risk Control works closely with departments such as operations, legal, compliance, and finance to identify, assess, and mitigate risks across the organization. This role often involves leading cross-functional meetings, developing training programs, and ensuring that risk control policies are integrated into daily business processes. Effective collaboration requires strong communication skills, as the Director must translate complex risk concepts into actionable steps for various teams. Regular reporting and feedback loops help ensure that risk management strategies remain aligned with organizational goals and regulatory requirements.

What is the difference between Director Of Risk Control vs Risk Analyst?

AspectDirector Of Risk ControlRisk Analyst
CredentialsBachelor's degree, often advanced certifications (e.g., ARM, CPCU)Bachelor's degree, often certifications like CRM or FRM
Work EnvironmentStrategic planning, leadership, cross-department collaborationData analysis, risk assessment, report preparation
Employer & IndustryInsurance, finance, large corporationsInsurance, finance, consulting firms
Search & Comparison IntentUnderstanding leadership roles in risk managementAnalyzing risk data and assessments

The main difference is that the Director Of Risk Control oversees risk management strategies and leads teams, while a Risk Analyst focuses on analyzing data to identify and assess risks. The director has broader responsibilities and strategic oversight, whereas the analyst is more involved in data-driven risk evaluation.

What job categories do people searching Director Of Risk Control jobs in Athens, GA look for?

The top searched job categories for Director Of Risk Control jobs in Athens, GA are:

What cities near Athens, GA are hiring for Director Of Risk Control jobs?

Cities near Athens, GA with the most Director Of Risk Control job openings:

Director Of Risk Control jobs near you
Infographic showing various Director Of Risk Control job openings in Athens, GA as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 72% Full Time, 23% Part Time, 2% Contract, and 1% Nights. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $136,159 per year, or $65.5 per hour.

Quality Control Manager

Alexion Pharmaceuticals

Bogart, GA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 29 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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