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Chemical Risk Assessment Jobs in Atlanta, GA (NOW HIRING)

Call Center Specialist Weekends Part Time

Atlanta, GA · On-site

$79K - $79K/yr

... risk assessment, psychiatric diagnoses symptomology, basic chemical dependency, age specific growth and development and crisis and behavior management. EEO Statement All UHS subsidiaries are ...

Conduct regular workplace inspections and risk assessments to identify hazards, specifically ... chemical spill, etc.). * Ensure that emergency equipment (e.g., fire extinguishers, first aid kits ...

Conduct regular workplace inspections and risk assessments to identify hazards, specifically ... chemical spill, etc.). * Ensure that emergency equipment (e.g., fire extinguishers, first aid kits ...

... risk assessment, psychiatric diagnoses symptomology, basic chemical dependency, age specific growth and development and crisis and behavior management. EEO Statement All UHS subsidiaries are ...

... risk assessment, psychiatric diagnoses symptomology, basic chemical dependency, age specific growth and development and crisis and behavior management. EEO Statement All UHS subsidiaries are ...

Conduct feasibility studies, cost analysis, and risk assessments for new processes or equipment ... Bachelor's degree in Chemical Engineering, Mechanical Engineering, Industrial Engineering, or a ...

Conduct feasibility studies, cost analysis, and risk assessments for new processes or equipment ... Bachelor's degree in Chemical Engineering, Mechanical Engineering, Industrial Engineering, or a ...

EHS Manager

Lithia Springs, GA · On-site

$76K - $103K/yr

Risk Assessment -Identifies potential hazards, assesses risks, and implements preventive measures ... and chemical safety. * Ergonomics - Applies ergonomic principles to prevent workplace injuries ...

... Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance ... Lead design reviews, risk assessments, and FMEA to ensure reliability and performance. * Ensure ...

Showing results 21-40

Chemical Risk Assessment information

What is chemical risk assessment?

Chemical risk assessment is the process of evaluating the potential adverse health and environmental effects caused by exposure to chemicals. This involves identifying hazards, assessing how and where people or the environment may be exposed, determining the level of risk, and recommending ways to manage or mitigate those risks. Chemical risk assessment is crucial in regulatory decision-making, workplace safety, and environmental protection. Professionals in this field use scientific data, exposure models, and toxicological information to inform policy and safeguard public health.

What are some typical challenges faced by professionals in chemical risk assessment roles, and how can they be addressed?

Professionals in Chemical Risk Assessment often encounter challenges such as interpreting complex toxicological data, keeping up with evolving regulatory requirements, and effectively communicating risks to both technical and non-technical stakeholders. Addressing these challenges involves continuous learning, close collaboration with regulatory experts and scientists, and developing strong communication skills to present findings clearly. Working in multidisciplinary teams also helps ensure that assessments are comprehensive and aligned with organizational and legal standards.

What are the key skills and qualifications needed to thrive as a chemical risk assessor, and why are they important?

To thrive as a Chemical Risk Assessor, you need a solid background in chemistry, toxicology, and environmental science, typically supported by a relevant degree. Familiarity with risk assessment models, regulatory databases, and statistical analysis software such as EPA’s EPI Suite or OECD tools is essential. Strong analytical thinking, attention to detail, and effective communication skills are vital for interpreting data and conveying complex findings to stakeholders. These skills are crucial to ensure the accurate evaluation of chemical hazards and compliance with safety regulations, ultimately protecting public health and the environment.

What is the difference between Chemical Risk Assessment vs Chemical Safety Specialist?

AspectChemical Risk AssessmentChemical Safety Specialist
Primary FocusEvaluating chemical hazards and risks to health and environmentImplementing safety protocols and ensuring compliance in chemical handling
Required CredentialsDegree in chemistry, toxicology, or related field; risk assessment certificationsSimilar credentials; safety certifications like OSHA or HAZWOPER
Work EnvironmentLaboratories, risk assessment teams, regulatory agenciesIndustrial sites, manufacturing plants, safety departments
Industry UsageRegulatory compliance, environmental agencies, consultingIndustrial companies, chemical plants, safety consulting

While both roles involve chemical safety, Chemical Risk Assessment focuses on analyzing hazards and determining risks, whereas Chemical Safety Specialist emphasizes implementing safety measures and ensuring compliance in workplaces.

What are popular job titles related to Chemical Risk Assessment jobs in Atlanta, GA?

For Chemical Risk Assessment jobs in Atlanta, GA, the most frequently searched job titles are:

What job categories do people searching Chemical Risk Assessment jobs in Atlanta, GA look for?

The top searched job categories for Chemical Risk Assessment jobs in Atlanta, GA are:

Infographic showing various Chemical Risk Assessment job openings in Atlanta, GA as of July 2026, with employment types broken down into 1% As Needed, 86% Full Time, 10% Part Time, and 3% Contract. Highlights an 89% Physical, 4% Hybrid, and 7% Remote job distribution.

CLIA Compliance Analyst II

Chenega Corporation

Atlanta, GA • On-site, Remote

Full-time

Posted 8 days ago


Job description

Overview
Come join a company that strives for Extraordinary People and Exceptional Performance! Chenega Enterprise Systems & Solutions, LLC, a Chenega Professional Services' company, is looking for a CLIA Compliance Analyst II to support the Office of Laboratory Quality (OLQ) which provides strategic guidance and leadership on infectious disease issues, managing the operations of various centers, including the National Center for Emerging and Zoonotic Infectious Diseases (NCEZID), the National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention (NCHHSTP), and the National Center for Immunization and Respiratory Diseases (NCIRD). The purpose of this role is to provide quality management support.
Our company offers employees the opportunity to join a team where there is a robust employee benefits program, management engagement, quality leadership, an atmosphere of teamwork, recognition for performance, and promotion opportunities. We actively strive to channel our highly engaged employee's knowledge, critical thinking, innovative solutions for our clients.
Location: Due to CDC's telework posture, work will be primarily performed in a remote environment for the foreseeable future, with periodic and/or monthly/quarterly in-person meetings, and in-person internal assessments of ID laboratory documents and records. The primary location address is: 1600 Clifton Rd NE, Roybal Campus, Atlanta, GA 30329
Responsibilities
  • Conduct annual ID laboratory audits of each of approximately 25 CDC Atlanta ID laboratory branches for adherence to CLIA regulations and QMS to determine potential areas of vulnerabilities that may pose a risk to the agency.
  • Support CDC ID laboratories through maintaining and improving internal consultation services (e.g., e-mail, Microsoft Form submission), providing actionable feedback to stakeholders (ID laboratory staff, ID laboratory leadership and OLSR/OLQ).
  • Assist with the creation of tools and resources (e.g., procedures, forms, templates) for ID laboratory compliance and the Test Directory (client services menu) that support standardization throughout CDC ID laboratories.
  • Maintain and improve the process for submission, review, and approval of test method validation studies to establish test performance characteristics (e.g., specificity, precision, reproducibility) for clinical and surveillance test systems.
  • Work with task lead to maintain and improve communication processes between OLSR/OLQ, ID laboratory staff and ID laboratory leadership, towards improving overall quality of ID laboratory testing at CDC. The contractor shall develop solutions that improve communication and customer service to testing laboratories.
  • Develop CLIA-related documents and processes, support external inspections, and develop CLIA-related training for laboratory staff.
  • Create tools and resources for compliance to quality standards, and support laboratories with consultations.
  • Conduct coordinated CLIA and quality audits for adherence to CLIA regulations and CDC quality standards, develop and support external reviews and findings, work with ID laboratories on corrective actions.
  • Collaborate with laboratory management to implement corrective actions and continuous improvement initiatives based on audit findings and regulatory changes.
  • Review data and evaluate for test specificity, precision, and reproducibility as well as other performance characteristics to confirm test is fit for purpose. Document review process and approvals of assay development and validation data.
  • Make recommendations where physical ID laboratory processes, system and infrastructure requirements, quality management guidelines, and protocols could be updated to mitigate frequency of non-conforming events surrounding ID laboratory data.
  • Maintain the CDC ID Test Directory (client services menu) housed on externally facing CDC servers, initiate test order updates, provide recommendations and solutions to improve the ID test order directory update process and recurring update cycle.
  • Risk Assessment. Identify potential compliance risks and work with relevant departments to develop mitigation strategies.
  • Contractor shall travel to CDC facilities for the purpose of conducting the 25 annual laboratory audits.
  • Other duties as assigned

Qualifications
  • Minimum Qualifications: (To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.)
    • Bachelor's degree in a relevant field chemical, physical, biological or clinical laboratory science.
    • 4+ years experience in a diagnostic laboratory or other similar regulated environment performing or supervising high complexity microbiology with a minimum of 6 months in subspecialty of service.
    • Previous auditing experience preferred. At least 3-5 years of experience in a compliance or regulatory role within a clinical laboratory or healthcare setting, with a strong understanding of CLIA regulations.
    • ASCP, AMT, or AAB Board Certification preferred.

    Knowledge, Skills and Abilities:
    • Manage laboratory accreditations and certifications.
    • Able to understand and apply new regulations.
    • Experience with or knowledge of Quality Assurance procedures.
    • Must be attentive to detail and organized, especially related to documentation and record-keeping.
    • Familiarity with CLIA regulations and standards.
    • Ability and judgment to interact and communicate appropriately with other employees, clients, and management.
    • Excellent interpersonal, verbal, and written communication skills. Proven track record and experience in building and cultivating strong relationships.
    • Ability to organize data and generate reports.

Teleworking Permitted?
Yes
Teleworking Details
Due to CDC's telework posture, work will be primarily performed in a remote environment for the foreseeable future, with periodic and/or monthly/quarterly in-person meetings, and in-person internal assessments of ID laboratory documents and records.
Estimated Salary/Wage
USD $73,000.00/Yr. Up to USD $75,000.00/Yr.