... • Supports FDA inspections, IND/IDE application reviews, stem cell reviews and other research regulatory assistance as needed MINIMUM QUALIFICATIONS: * Bachelor's degree and five years of ...
... • Supports FDA inspections, IND/IDE application reviews, stem cell reviews and other research regulatory assistance as needed MINIMUM QUALIFICATIONS: * Bachelor's degree and five years of ...
Supports FDA inspections, IND/IDE application reviews, stem cell reviews and other research regulatory assistance as needed MINIMUM QUALIFICATIONS: * Bachelor's degree and five years of experience in ...
Supports FDA inspections, IND/IDE application reviews, stem cell reviews and other research regulatory assistance as needed MINIMUM QUALIFICATIONS: * Bachelor's degree and five years of experience in ...
... • Supports FDA inspections, IND/IDE application reviews, stem cell reviews and other research regulatory assistance as needed MINIMUM QUALIFICATIONS: * Bachelor's degree and five years of ...
... • Supports FDA inspections, IND/IDE application reviews, stem cell reviews and other research regulatory assistance as needed MINIMUM QUALIFICATIONS: * Bachelor's degree and five years of ...
... FDA QMSR, ISO 13485, IVDR, MDSAP, auditing, CAPA, and quality systems. * Strong leadership, coaching, communication, and project management skills. * Experience leading inspections and external ...
... FDA QMSR, ISO 13485, IVDR, MDSAP, auditing, CAPA, and quality systems. * Strong leadership, coaching, communication, and project management skills. * Experience leading inspections and external ...
Ensure compliance with FDA 21 CFR Part 11, EU Annex 11, GAMP 5, ALCOA+ Data Integrity principles ... Support regulatory inspections, customer audits, and internal compliance reviews, including ...
Ensure compliance with FDA 21 CFR Part 11, EU Annex 11, GAMP 5, ALCOA+ Data Integrity principles ... Support regulatory inspections, customer audits, and internal compliance reviews, including ...
Computer Systems Validation (CSV) IT Engineer (IT Support Specialist)
Tucker, GA · On-site
$96K - $115K/yr
Ensure compliance with FDA 21 CFR Part 11, EU Annex 11, GAMP 5, ALCOA+ Data Integrity principles ... Support regulatory inspections, customer audits, and internal compliance reviews, including ...
Computer Systems Validation (CSV) IT Engineer (IT Support Specialist)
Tucker, GA · On-site
$96K - $115K/yr
Ensure compliance with FDA 21 CFR Part 11, EU Annex 11, GAMP 5, ALCOA+ Data Integrity principles ... Support regulatory inspections, customer audits, and internal compliance reviews, including ...
Ensure compliance with FDA 21 CFR Part 11, EU Annex 11, GAMP 5, ALCOA+ Data Integrity principles ... Support regulatory inspections, customer audits, and internal compliance reviews, including ...
Ensure compliance with FDA 21 CFR Part 11, EU Annex 11, GAMP 5, ALCOA+ Data Integrity principles ... Support regulatory inspections, customer audits, and internal compliance reviews, including ...
Ensure data integrity and compliance with GCP, FDA, MDR/IVDR, and other applicable regulatory ... Support audit readiness and participate in regulatory inspections when required. * Mentor junior ...
Ensure data integrity and compliance with GCP, FDA, MDR/IVDR, and other applicable regulatory ... Support audit readiness and participate in regulatory inspections when required. * Mentor junior ...
Ensure compliance with FDA 21 CFR Part 11, EU Annex 11, GAMP 5, ALCOA+ Data Integrity principles ... Support regulatory inspections, customer audits, and internal compliance reviews, including ...
Ensure compliance with FDA 21 CFR Part 11, EU Annex 11, GAMP 5, ALCOA+ Data Integrity principles ... Support regulatory inspections, customer audits, and internal compliance reviews, including ...
... FDA QMSR, ISO 13485, IVDR, MDSAP, auditing, CAPA, and quality systems. * Strong leadership, coaching, communication, and project management skills. * Experience leading inspections and external ...
... FDA QMSR, ISO 13485, IVDR, MDSAP, auditing, CAPA, and quality systems. * Strong leadership, coaching, communication, and project management skills. * Experience leading inspections and external ...
... FDA QMSR, ISO 13485, IVDR, MDSAP, auditing, CAPA, and quality systems. * Strong leadership, coaching, communication, and project management skills. * Experience leading inspections and external ...
... FDA QMSR, ISO 13485, IVDR, MDSAP, auditing, CAPA, and quality systems. * Strong leadership, coaching, communication, and project management skills. * Experience leading inspections and external ...
... FDA QMSR, ISO 13485, IVDR, MDSAP, auditing, CAPA, and quality systems. * Strong leadership, coaching, communication, and project management skills. * Experience leading inspections and external ...
... FDA QMSR, ISO 13485, IVDR, MDSAP, auditing, CAPA, and quality systems. * Strong leadership, coaching, communication, and project management skills. * Experience leading inspections and external ...
... FDA QMSR, ISO 13485, IVDR, MDSAP, auditing, CAPA, and quality systems. * Strong leadership, coaching, communication, and project management skills. * Experience leading inspections and external ...
... FDA QMSR, ISO 13485, IVDR, MDSAP, auditing, CAPA, and quality systems. * Strong leadership, coaching, communication, and project management skills. * Experience leading inspections and external ...
Be Seen First
Bottle Making Supervisor
White, GA · On-site
$75K/yr
Maintain high sanitation and workplace safety standards in compliance with SQF,HACCP,FDA requirements and OSHA regulations to ensure readiness for third-party audits and regulatory inspections.
Quick apply
Be Seen First
Bottle Making Supervisor
White, GA · On-site
$75K/yr
Maintain high sanitation and workplace safety standards in compliance with SQF,HACCP,FDA requirements and OSHA regulations to ensure readiness for third-party audits and regulatory inspections.
Factory Facility Supervisor
White, GA · On-site
$75K/yr
Maintain high sanitation and workplace safety standards in compliance with SQF, HACCP, FDA requirements and OSHA regulations to ensure readiness for third-party audits and regulatory inspections.
Quick apply
Factory Facility Supervisor
White, GA · On-site
$75K/yr
Maintain high sanitation and workplace safety standards in compliance with SQF, HACCP, FDA requirements and OSHA regulations to ensure readiness for third-party audits and regulatory inspections.
Be Seen First
Production Supervisor
White, GA · On-site
$75K/yr
Maintain high sanitation and workplace safety standards in compliance with SQF,HACCP,FDA requirements and OSHA regulations to ensure readiness for third-party audits and regulatory inspections.
Quick apply
Be Seen First
Production Supervisor
White, GA · On-site
$75K/yr
Maintain high sanitation and workplace safety standards in compliance with SQF,HACCP,FDA requirements and OSHA regulations to ensure readiness for third-party audits and regulatory inspections.
Be Seen First
Filling and Packaging Supervisor
White, GA · On-site
$75K/yr
Maintain high sanitation and workplace safety standards in compliance with SQF,HACCP,FDA requirements and OSHA regulations to ensure readiness for third-party audits and regulatory inspections.
Quick apply
Be Seen First
Filling and Packaging Supervisor
White, GA · On-site
$75K/yr
Maintain high sanitation and workplace safety standards in compliance with SQF,HACCP,FDA requirements and OSHA regulations to ensure readiness for third-party audits and regulatory inspections.
Sr. Clinical Data Manager
Kennesaw, GA · On-site
Ensure data integrity and compliance with GCP, FDA, MDR/IVDR, and other applicable regulatory ... Support audit readiness and participate in regulatory inspections when required. * Mentor junior ...
Sr. Clinical Data Manager
Kennesaw, GA · On-site
Ensure data integrity and compliance with GCP, FDA, MDR/IVDR, and other applicable regulatory ... Support audit readiness and participate in regulatory inspections when required. * Mentor junior ...
Maintain high sanitation and workplace safety standards in compliance with SQF, HACCP, FDA requirements and OSHA regulations to ensure readiness for third-party audits and regulatory inspections.
Quick apply
Maintain high sanitation and workplace safety standards in compliance with SQF, HACCP, FDA requirements and OSHA regulations to ensure readiness for third-party audits and regulatory inspections.
US Operator
Alpharetta, GA · On-site
$24.04/hr
The technician will perform assembly, inspection, packaging, and documentation tasks in accordance with GMP, ISO 13485, and FDA regulations. This role is critical to ensuring product quality ...
US Operator
Alpharetta, GA · On-site
$24.04/hr
The technician will perform assembly, inspection, packaging, and documentation tasks in accordance with GMP, ISO 13485, and FDA regulations. This role is critical to ensuring product quality ...
Fda Inspector information
See Atlanta, GA salary details
$23.6K - $30.1K
3% of jobs
$30.1K - $36.6K
16% of jobs
$38.2K is the 25th percentile. Wages below this are outliers.
$36.6K - $43.1K
23% of jobs
The median wage is $45.1K / yr.
$43.1K - $49.6K
27% of jobs
$53.8K is the 75th percentile. Wages above this are outliers.
$49.6K - $56.1K
10% of jobs
$56.1K - $62.6K
4% of jobs
$62.6K - $69.2K
5% of jobs
$69.2K - $75.7K
2% of jobs
$75.7K - $82.2K
2% of jobs
$82.2K - $88.7K
2% of jobs
$88.7K - $95.2K
5% of jobs
$23.6K
$52.8K
$95.2K
How much do fda inspector jobs pay per year?
How much do FDA drug investigators make?
What types of facilities or products do FDA Inspectors typically review, and what does a typical inspection process involve?
FDA Inspectors routinely examine a variety of facilities, such as food processing plants, pharmaceutical manufacturers, medical device companies, and cosmetic production sites, to ensure compliance with federal safety and quality regulations. A typical inspection involves reviewing operational procedures, examining production environments, sampling products, and interviewing staff to identify potential violations or risks. Inspectors often work onsite, sometimes with travel required to cover multiple locations within their region, and collaborate closely with facility management to explain findings and recommend corrective actions. This role offers the opportunity to make a significant impact on public health and provides clear advancement pathways into specialized inspection or supervisory roles within regulatory agencies.
What are the key skills and qualifications needed to thrive in the Fda Inspector position, and why are they important?
To thrive as an FDA Inspector, you need a solid background in science or public health, attention to detail, and thorough knowledge of regulatory standards, often supported by a relevant degree. Familiarity with inspection protocols, laboratory testing equipment, and digital reporting systems is commonly required, along with potential USDA or FDA certifications. Strong analytical thinking, effective communication, and integrity are important soft skills for this role. These competencies ensure accurate inspections, compliance with safety regulations, and clear reporting essential to public health and organizational accountability.
What type of inspector gets paid the most?
Is it hard to get a job at FDA?
How do you become an FDA inspector?
What does an FDA Inspector do?
An FDA Inspector is responsible for ensuring that companies comply with federal regulations related to food, drugs, medical devices, and other products overseen by the U.S. Food and Drug Administration. They conduct inspections, review records, collect samples, and assess manufacturing practices to ensure public health and safety. Inspectors may also investigate complaints, issue compliance notices, and recommend enforcement actions if violations are found.

Full-time
Posted 18 days ago
Emory Healthcare rating
7.7
Based on 212 frontline employees who took The Breakroom Quiz
159th of 888 rated healthcare providers
Job description
Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future. We welcome candidates who can contribute to the excellence of our academic community.
Description
JOB DESCRIPTION:
- The Senior Research Compliance Specialist ensures institutional compliance with federal, state, sponsor, and university research regulations and policies.
- This role conducts compliance reviews and risk assessments, supports investigations and issue resolution, provides training and guidance, and contributes to the development and continuous improvement of research compliance programs.
- The position partners closely with faculty, research staff, and central administration to promote a strong culture of compliance and responsible research conduct.
- Senior Research Compliance Specialists may be assigned one or more regulatory specializations based on institutional needs.
- These specializations define the primary regulatory focus and required subject-matter expertise for the role, such as research integrity, controlled substances, research cybersecurity, or research security.
- Conducts risk-based reviews, audits, and monitoring of research activities to assess compliance with applicable regulations, sponsor requirements, and institutional policies.
- Supports and manages investigations and issue resolution related to research compliance, including documentation, analysis, reporting, and corrective and preventive actions.
- Develops, implements, and maintains research compliance policies, procedures, guidance, and operational tools.
- Provides training, education, and consultative support to faculty, research staff, and administrators on research compliance requirements.
- Prepares reports, metrics, and documentation to support compliance monitoring, program evaluation, and leadership reporting.
- Maintains accurate and secure program records and ensures the integrity and confidentiality of sensitive information.
- Collaborates with departments, committees, central offices, and external partners (e.g., IT, vendors) to support research compliance programs and enterprise systems.
- Contributes to continuous improvement of research compliance programs and promotes a positive culture of compliance and responsible research conduct.
- Performs related responsibilities as required.
Regulatory Specialization:
The Senior Research Compliance Specialist may be assigned one or more regulatory specializations based on institutional needs. Regulatory specializations define the primary regulatory domain and subject-matter expertise required for the role and do not change the underlying job classification.
Research Integrity
• Supports intake, assessment, and review of research misconduct allegations.
• Assists with research integrity investigations, including evidence review, interviews, documentation, and reporting.
• Provides guidance on research integrity policies, procedures, and responsible conduct of research requirements.
• Supports FDA inspections, IND/IDE application reviews, stem cell reviews and other research regulatory assistance as needed
MINIMUM QUALIFICATIONS:
- Bachelor's degree and five years of experience in research administration, research compliance, internal audit, legal, audit, or a related field.
- Experience in a university or research environment involving heavily regulated industries preferred.
- Juris Doctorate or master's degree and Certified Compliance and Ethics Professional (CCEP), Certified in Healthcare Research Compliance (CHRC), or similar certification preferred.
NOTE: This role will be granted the opportunity to work from home regularly but must be able to commute to Emory University on a flexible weekly schedule based upon business needs. Schedule is based on agreed upon guidelines of department. This role requires residency in the state of GA. Emory reserves the right to change remote work status with notice to employee.
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Additional Details
Emory is an equal opportunity employer, and qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by state or federal law. Emory University does not discriminate in admissions, educational programs, or employment, including recruitment, hiring, promotions, transfers, discipline, terminations, wage and salary administration, benefits, and training. Students, faculty, and staff are assured of participation in university programs and in the use of facilities without such discrimination. Emory University complies with Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veteran's Readjustment Assistance Act, and applicable executive orders, federal and state regulations regarding nondiscrimination, equal opportunity, and affirmative action (for protected veterans and individuals with disabilities). Inquiries regarding this policy should be directed to the Emory University Department of Equity and Civil Rights Compliance, 201 Dowman Drive, Administration Building, Atlanta, GA 30322. Telephone: 404-727-9867 (V) | 404-712-2049 (TDD).
Emory University is committed to ensuring equal access and providing reasonable accommodations to qualified individuals with disabilities upon request. To request this document in an alternate format or to seek a reasonable accommodation, please contact the Department of Accessibility Services at accessibility@emory.edu or call 404-727-9877 (Voice) | 404-712-2049 (TDD). We kindly ask that requests be made at least seven business days in advance to allow adequate time for coordination.
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About Emory Health
Sourced by ZipRecruiter
Industry
Hospitals
Company size
10,000+ Employees
Headquarters location
NE Atlanta, GA, US
Year founded
1905