Medical Device Quality Systems & FDA Inspection Readiness Consultant Location: Atlanta/Duluth, Georgia area Work Arrangement: Onsite Duration: Immediate start through November 2026, with potential ...
Quick apply
Medical Device Quality Systems & FDA Inspection Readiness Consultant Location: Atlanta/Duluth, Georgia area Work Arrangement: Onsite Duration: Immediate start through November 2026, with potential ...
Quick apply
Medical Device Quality Systems & FDA Inspection Readiness Consultant Location: Atlanta/Duluth, Georgia area Work Arrangement: Onsite Duration: Immediate start through November 2026, with potential ...
Atlanta, GA · On-site
$100 - $125/hr
Manage inspection readiness and draft responses to FDA 483s. * Draft high‑level regulatory analyses and strategic client guidance memos. * Manage promotional and labeling review for FDA and FTC ...
Atlanta, GA · On-site
$100 - $125/hr
Manage inspection readiness and draft responses to FDA 483s. * Draft high‑level regulatory analyses and strategic client guidance memos. * Manage promotional and labeling review for FDA and FTC ...
Conley, GA · On-site
... FDA inspections and customer audits from preparation through resolution Drive strategic quality initiatives using systems thinking and cross-functional collaboration Partner with operations ...
Conley, GA · On-site
... FDA inspections and customer audits from preparation through resolution Drive strategic quality initiatives using systems thinking and cross-functional collaboration Partner with operations ...
Conley, GA · On-site
Lead USDA-FSIS/FDA inspections and customer audits from preparation through resolution * Drive strategic quality initiatives using systems thinking and cross-functional collaboration * Partner with ...
Quick apply
Conley, GA · On-site
Lead USDA-FSIS/FDA inspections and customer audits from preparation through resolution * Drive strategic quality initiatives using systems thinking and cross-functional collaboration * Partner with ...
Conley, GA · On-site
Proven experience leading USDA-FSIS/FDA inspections and customer audits * HACCP Certification, Seafood HACCP Certification (or obtain within 60 days), and PCQI Certification required * SQF ...
Conley, GA · On-site
Proven experience leading USDA-FSIS/FDA inspections and customer audits * HACCP Certification, Seafood HACCP Certification (or obtain within 60 days), and PCQI Certification required * SQF ...
Conley, GA · On-site
Proven experience leading USDA-FSIS/FDA inspections and customer audits * HACCP Certification, Seafood HACCP Certification (or obtain within 60 days), and PCQI Certification required * SQF ...
Conley, GA · On-site
Proven experience leading USDA-FSIS/FDA inspections and customer audits * HACCP Certification, Seafood HACCP Certification (or obtain within 60 days), and PCQI Certification required * SQF ...
Norcross, GA · On-site
$150 - $200/hr
Represent Supplier Quality during FDA inspections, ISO 13485/MDSAP audits, customer audits, and internal audits. * Present supplier quality performance, risks, trends, and improvement initiatives ...
Norcross, GA · On-site
$150 - $200/hr
Represent Supplier Quality during FDA inspections, ISO 13485/MDSAP audits, customer audits, and internal audits. * Present supplier quality performance, risks, trends, and improvement initiatives ...
Support FDA inspections, audits, and regulatory inquiries related to complaint handling * Ensure timely reporting of adverse events, product quality complaints, and potential reportable events (e.g ...
Support FDA inspections, audits, and regulatory inquiries related to complaint handling * Ensure timely reporting of adverse events, product quality complaints, and potential reportable events (e.g ...
Performs analysis of product quality inspection of parts, raw materials, and/or packaging ... ISO/FDA/GMP compliance. Skills: Qualifications Education: Additional Information For more ...
Performs analysis of product quality inspection of parts, raw materials, and/or packaging ... ISO/FDA/GMP compliance. Skills: Qualifications Education: Additional Information For more ...
Audit and Inspection Support * Assist in preparing for internal audits, external audits, supplier audits, and FDA inspections. * Help collect and organize documentation requested by auditors and ...
Audit and Inspection Support * Assist in preparing for internal audits, external audits, supplier audits, and FDA inspections. * Help collect and organize documentation requested by auditors and ...
Serve as quality site lead for FDA and customer inspections. Ensures inspection readiness at all times. * Address compliance issues and manage CAPAs effectively. * Promote accountability, data ...
Serve as quality site lead for FDA and customer inspections. Ensures inspection readiness at all times. * Address compliance issues and manage CAPAs effectively. * Promote accountability, data ...
Gainesville, GA · On-site
Serve as quality site lead for FDA and customer inspections. Ensures inspection readiness at all times. * Address compliance issues and manage CAPAs effectively. * Promote accountability, data ...
Gainesville, GA · On-site
Serve as quality site lead for FDA and customer inspections. Ensures inspection readiness at all times. * Address compliance issues and manage CAPAs effectively. * Promote accountability, data ...
Norcross, GA · On-site
$150 - $200/hr
Represent Supplier Quality during FDA inspections, ISO 13485/MDSAP audits, customer audits, and internal audits. * Present supplier quality performance, risks, trends, and improvement initiatives ...
Norcross, GA · On-site
$150 - $200/hr
Represent Supplier Quality during FDA inspections, ISO 13485/MDSAP audits, customer audits, and internal audits. * Present supplier quality performance, risks, trends, and improvement initiatives ...
Marietta, GA · On-site
Compliance Support Support Regulatory Affairs with submission documentation and compliance records Maintain quality documentation required for FDA and ISO compliance Support inspection readiness and ...
Marietta, GA · On-site
Compliance Support Support Regulatory Affairs with submission documentation and compliance records Maintain quality documentation required for FDA and ISO compliance Support inspection readiness and ...
Norcross, GA · On-site
$21 - $23/hr
Quality Control Inspector Reports to: Quality Control Supervisor Location: Norcross, GA (On-site ... Previous experience in a regulated industry is preferred (Example - other FDA controlled industry ...
Quick apply
Norcross, GA · On-site
$21 - $23/hr
Quality Control Inspector Reports to: Quality Control Supervisor Location: Norcross, GA (On-site ... Previous experience in a regulated industry is preferred (Example - other FDA controlled industry ...
Atlanta, GA · On-site
$150 - $200/hr
... FDA inspection readinessEnsure compliance with FDA regulations, ICH-GCP, HIPAA, institutional policies, and sponsor requirementsSet the roadmap for research technology, data governance, and ...
Atlanta, GA · On-site
$150 - $200/hr
... FDA inspection readinessEnsure compliance with FDA regulations, ICH-GCP, HIPAA, institutional policies, and sponsor requirementsSet the roadmap for research technology, data governance, and ...
Marietta, GA · On-site
$150 - $200/hr
Maintain quality documentation required for FDA and ISO compliance * Support inspection readiness and regulatory audit responses * Ensure quality system documentation supports product lifecycle and ...
Marietta, GA · On-site
$150 - $200/hr
Maintain quality documentation required for FDA and ISO compliance * Support inspection readiness and regulatory audit responses * Ensure quality system documentation supports product lifecycle and ...
Marietta, GA · On-site
$125 - $150/hr
Maintain quality documentation required for FDA and ISO compliance * Support inspection readiness and regulatory audit responses * Ensure quality system documentation supports product lifecycle and ...
Marietta, GA · On-site
$125 - $150/hr
Maintain quality documentation required for FDA and ISO compliance * Support inspection readiness and regulatory audit responses * Ensure quality system documentation supports product lifecycle and ...
Maintain oversight of the Quality Management System, SOPs, CAPA plans, audits, and FDA inspection readiness * Ensure compliance with FDA regulations, ICH-GCP, HIPAA, institutional policies, and ...
Maintain oversight of the Quality Management System, SOPs, CAPA plans, audits, and FDA inspection readiness * Ensure compliance with FDA regulations, ICH-GCP, HIPAA, institutional policies, and ...
Marietta, GA · On-site
Compliance Support Support Regulatory Affairs with submission documentation and compliance records Maintain quality documentation required for FDA and ISO compliance Support inspection readiness and ...
Marietta, GA · On-site
Compliance Support Support Regulatory Affairs with submission documentation and compliance records Maintain quality documentation required for FDA and ISO compliance Support inspection readiness and ...
$20.7K - $26.4K
3% of jobs
$26.4K - $32.1K
16% of jobs
$33.6K is the 25th percentile. Wages below this are outliers.
$32.1K - $37.8K
23% of jobs
The median wage is $39.6K / yr.
$37.8K - $43.6K
27% of jobs
$47.2K is the 75th percentile. Wages above this are outliers.
$43.6K - $49.3K
10% of jobs
$49.3K - $55K
4% of jobs
$55K - $60.7K
5% of jobs
$60.7K - $66.4K
2% of jobs
$66.4K - $72.2K
2% of jobs
$72.2K - $77.9K
2% of jobs
$77.9K - $83.6K
5% of jobs
$20.7K
$46.4K
$83.6K
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.
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.
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.
For Fda Inspector jobs in Georgia, the most frequently searched job titles are:
The top searched job categories for Fda Inspector jobs in Georgia are:
Cities in Georgia with the most Fda Inspector job openings:

Full-time
Posted 11 days ago
Medical Device Quality Systems & FDA Inspection Readiness Consultant
Location: Atlanta/Duluth, Georgia area
Work Arrangement: Onsite
Duration: Immediate start through November 2026, with potential extension
Start: Immediate
Position Overview
We are seeking an experienced Medical Device Quality Systems Consultant to provide hands-on support for the startup of a new Class I medical device contract manufacturing operation.
The consultant will support Quality Management System (QMS) implementation, development of auditable quality and operational processes, system validation, and FDA inspection readiness. A key focus will be ensuring appropriate controls are established across production, warehousing, inventory, traceability, product hold/quarantine, release, and direct-to-consumer distribution activities.
The engagement will require both quality systems expertise and practical implementation support as the organization works toward regulatory and operational milestones in October and a planned November 1 go-live. The consultant may also provide training and ongoing Quality support following launch.
Key Responsibilities
Review the existing QMS and tailor requirements and processes for the new medical device manufacturing operation.
Support implementation of the QMS and ensure processes are operational, documented, and auditable.
Develop new quality and operational processes needed to support manufacturing and distribution activities.
Support validation of the warehouse management system and associated workflows.
Establish and/or assess controls for production, inventory management, product traceability, quarantine/hold, and product release.
Develop appropriate quality checks and controls for direct-to-consumer product shipments.
Assess Quality System and operational readiness for an anticipated FDA inspection.
Identify inspection-readiness gaps and support implementation of corrective actions before go-live.
Work directly with facility personnel to operationalize new procedures and quality controls.
Provide employee training and implementation support for new or revised processes, as needed.
Support the organization through its planned November 1 launch and provide ongoing Quality support following go-live, as needed.
Required Qualifications
Significant medical device Quality or Quality Systems experience.
Demonstrated experience implementing or adapting a QMS for medical device operations.
Strong knowledge of FDA medical device quality requirements and inspection readiness.
Experience developing and implementing auditable quality and operational processes.
Experience with warehouse, distribution, inventory, traceability, quarantine/hold, and product release controls.
Experience supporting computerized system validation or validation of warehouse/inventory management systems.
Ability to provide hands-on implementation support and work directly with site personnel.
Ability to work onsite in the Atlanta/Duluth, Georgia area.
Preferred Qualifications
Experience supporting startup or launch activities for a medical device manufacturing operation.
Experience with Class I medical devices.
Experience establishing quality controls for direct-to-consumer distribution.
Local to the Atlanta/Duluth, Georgia area.
Work Arrangement
This engagement requires onsite support in the Atlanta/Duluth, Georgia area. Local consultants are preferred to facilitate consistent onsite support.
Ideal Candidate
The ideal consultant is a hands-on Medical Device Quality Systems professional with experience taking QMS requirements from documented procedures through practical implementation. The consultant should be comfortable working across quality systems, warehouse and distribution controls, system validation, and FDA inspection readiness while helping a new manufacturing operation prepare for launch.
Sourced by ZipRecruiter
Recruiting and staffing services
11 - 50 Employees
Westborough, MA, US
2007