We are seeking a highly experienced Subcontractor - Senior OTC Compliance Auditor with a background as a former FDA Investigator/Inspector. This short-term assignment (May-August 2026) requires ...
We are seeking a highly experienced Subcontractor - Senior OTC Compliance Auditor with a background as a former FDA Investigator/Inspector. This short-term assignment (May-August 2026) requires ...
We are seeking a highly experienced Subcontractor - Senior OTC Compliance Auditor with a background as a former FDA Investigator/Inspector. This short-term assignment (May-August 2026) requires ...
We are seeking a highly experienced Subcontractor - Senior OTC Compliance Auditor with a background as a former FDA Investigator/Inspector. This short-term assignment (May-August 2026) requires ...
GCP/GMP Auditor - Former FDA / FDA Inspection Experience (Midwest USA)
Indianapolis, IN · On-site
$4K - $5K/wk
This engagement will simulate an FDA inspection environment , requiring an auditor who understands FDA expectations, inspection readiness, and compliance risks across GCP and GMP operations . The ...
GCP/GMP Auditor - Former FDA / FDA Inspection Experience (Midwest USA)
Indianapolis, IN · On-site
$4K - $5K/wk
This engagement will simulate an FDA inspection environment , requiring an auditor who understands FDA expectations, inspection readiness, and compliance risks across GCP and GMP operations . The ...
GCP/GMP Auditor - Former FDA / FDA Inspection Experience (Midwest USA)
Indianapolis, IN · On-site
$4K - $5K/wk
This engagement will simulate an FDA inspection environment , requiring an auditor who understands FDA expectations, inspection readiness, and compliance risks across GCP and GMP operations . The ...
GCP/GMP Auditor - Former FDA / FDA Inspection Experience (Midwest USA)
Indianapolis, IN · On-site
$4K - $5K/wk
This engagement will simulate an FDA inspection environment , requiring an auditor who understands FDA expectations, inspection readiness, and compliance risks across GCP and GMP operations . The ...
Senior CAPA FDA Lead
Bothell, WA · On-site
Lead FDA audit and inspection readiness activities across the business. * Own and present CAPA effectiveness, investigation quality, risk assessments, and HHE processes during FDA interactions. * Act ...
Quick apply
Senior CAPA FDA Lead
Bothell, WA · On-site
Lead FDA audit and inspection readiness activities across the business. * Own and present CAPA effectiveness, investigation quality, risk assessments, and HHE processes during FDA interactions. * Act ...
Complete annual training and certification to maintain FDA Commissioned Inspector status. * Attend regular program meetings and refresher training sessions to stay updated on federal and state ...
Complete annual training and certification to maintain FDA Commissioned Inspector status. * Attend regular program meetings and refresher training sessions to stay updated on federal and state ...
Complete annual training and certification to maintain FDA Commissioned Inspector status. * Attend regular program meetings and refresher training sessions to stay updated on federal and state ...
Complete annual training and certification to maintain FDA Commissioned Inspector status. * Attend regular program meetings and refresher training sessions to stay updated on federal and state ...
Complete annual training and certification to maintain FDA Commissioned Inspector status. * Attend regular program meetings and refresher training sessions to stay updated on federal and state ...
Complete annual training and certification to maintain FDA Commissioned Inspector status. * Attend regular program meetings and refresher training sessions to stay updated on federal and state ...
Complete annual training and certification to maintain FDA Commissioned Inspector status. * Attend regular program meetings and refresher training sessions to stay updated on federal and state ...
Quick apply
Complete annual training and certification to maintain FDA Commissioned Inspector status. * Attend regular program meetings and refresher training sessions to stay updated on federal and state ...
Complete annual training and certification to maintain FDA Commissioned Inspector status. * Attend regular program meetings and refresher training sessions to stay updated on federal and state ...
Quick apply
Complete annual training and certification to maintain FDA Commissioned Inspector status. * Attend regular program meetings and refresher training sessions to stay updated on federal and state ...
Tobacco Compliance Inspector assists the FDA in enforcing retail establishments compliance with the Tobacco Control Act, particularly as it relates to a reduction in youth tobacco use and access ...
Tobacco Compliance Inspector assists the FDA in enforcing retail establishments compliance with the Tobacco Control Act, particularly as it relates to a reduction in youth tobacco use and access ...
FDA Technical Consultant
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FDA Technical Consultant
Washington, DC · On-site +1
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Support preparation for FDA inspections and notified body audits * Review and author SOPs, technical documentation, and quality records * Advise on risk management processes and product lifecycle ...
Quick apply
Support preparation for FDA inspections and notified body audits * Review and author SOPs, technical documentation, and quality records * Advise on risk management processes and product lifecycle ...
Support preparation for FDA inspections and notified body audits * Review and author SOPs, technical documentation, and quality records * Advise on risk management processes and product lifecycle ...
Support preparation for FDA inspections and notified body audits * Review and author SOPs, technical documentation, and quality records * Advise on risk management processes and product lifecycle ...
FDA Tobacco Compliance Inspector
$30 - $31/hr
The inspection is used to establish a retailer's compliance with federal regulations. This work is ... and Drug Administration (FDA). * Learn more about this program by visiting: * Position is ...
New
Quick apply
FDA Tobacco Compliance Inspector
$30 - $31/hr
The inspection is used to establish a retailer's compliance with federal regulations. This work is ... and Drug Administration (FDA). * Learn more about this program by visiting: * Position is ...
New
Regulatory Affairs Specialist (FDA, DEA )
Irvine, CA · On-site
$60K - $76K/yr
Support internal audits, site inspections, and responses to 483s or warning letters * Coordinate ... Working knowledge of FDA regulations (21 CFR Parts 210, 211, 820) and DEA requirements * Strong ...
Regulatory Affairs Specialist (FDA, DEA )
Irvine, CA · On-site
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FDA Technical Consultant
Washington, DC · On-site
Prepare clients for inspections, provide inspection support (remote and on-site) * Provide technical support for remediation efforts in response to Form FDA 483s, Warning Letters, and other ...
FDA Technical Consultant
Washington, DC · On-site
Prepare clients for inspections, provide inspection support (remote and on-site) * Provide technical support for remediation efforts in response to Form FDA 483s, Warning Letters, and other ...
Quality Inspector
Buffalo Grove, IL · On-site
$50K - $60K/yr
Comply with applicable FDA regulations and ISO 13485 requirements. * Adhere to company Quality ... Creates inspection documents and maintains the incoming inspection room. * Verify that documents ...
Quick apply
Quality Inspector
Buffalo Grove, IL · On-site
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Comply with applicable FDA regulations and ISO 13485 requirements. * Adhere to company Quality ... Creates inspection documents and maintains the incoming inspection room. * Verify that documents ...
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Prepare clients for inspections, provide inspection support (remote and on-site) * Provide technical support for remediation efforts in response to Form FDA 483s, Warning Letters, and other ...
FDA Technical Consultant
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Regulatory Affairs Specialist (FDA, DEA )
Irvine, CA · On-site
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Support internal audits, site inspections, and responses to 483s or warning letters * Coordinate ... Working knowledge of FDA regulations (21 CFR Parts 210, 211, 820) and DEA requirements * Strong ...
Quick apply
Regulatory Affairs Specialist (FDA, DEA )
Irvine, CA · On-site
$60K - $76K/yr
Support internal audits, site inspections, and responses to 483s or warning letters * Coordinate ... Working knowledge of FDA regulations (21 CFR Parts 210, 211, 820) and DEA requirements * Strong ...
Fda Inspector information
See salary details
$24.5K - $31.3K
3% of jobs
$31.3K - $38K
16% of jobs
$39.7K is the 25th percentile. Wages below this are outliers.
$38K - $44.8K
23% of jobs
The median wage is $46.9K / yr.
$44.8K - $51.6K
27% of jobs
$55.9K is the 75th percentile. Wages above this are outliers.
$51.6K - $58.4K
10% of jobs
$58.4K - $65.1K
4% of jobs
$65.1K - $71.9K
5% of jobs
$71.9K - $78.7K
2% of jobs
$78.7K - $85.5K
2% of jobs
$85.5K - $92.2K
2% of jobs
$92.2K - $99K
5% of jobs
$24.5K
$54.9K
$99K
How much do fda inspector jobs pay per year?
What does an FDA Inspector do?
What are the key skills and qualifications needed to thrive in the Fda Inspector position, and why are they important?
What types of facilities or products do FDA Inspectors typically review, and what does a typical inspection process involve?
- What are the key skills and qualifications needed to thrive in the Fda Inspector position and why are they important?
- What does an FDA Inspector do?
- What types of facilities or products do FDA Inspectors typically review and what does a typical inspection process involve?
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Subcontractor - Senior OTC Compliance Auditor (Great opportunity for former FDA Inspectors)
SGSRemote
Full-time
Posted 18 hours ago
Job description
We are SGS - the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world.
Job Description
We are seeking a highly experienced Subcontractor - Senior OTC Compliance Auditor with a background as a former FDA Investigator/Inspector. This short-term assignment (May-August 2026) requires expertise in OTC drug manufacturing, cGMP compliance, and FDA inspection methodology.
As a subcontractor, you will support audits, inspection readiness activities, and compliance reviews for clients in the OTC pharmaceutical industry.
Key Responsibilities
- Conduct cGMP compliance audits of OTC drug manufacturing, packaging, labeling, and laboratory operations.
- Apply FDA inspection methodology to identify compliance gaps, risks, and deficiencies.
- Prepare detailed, professional audit reports outlining observations and recommended corrective actions.
- Support clients with mock FDA inspections, inspection readiness activities, and compliance remediation.
- Review quality systems, SOPs, batch records, data integrity controls, and laboratory practices.
- Represent the organization professionally during international client engagements.
- Manage scheduling, travel, and deliverables independently as an external contractor
Qualifications
- Former FDA Investigator/Inspector (required).
- 3-5 years of auditing experience within OTC or pharmaceutical manufacturing.
- Strong understanding of cGMP requirements, OTC monograph expectations, and FDA enforcement practices.
- Proven ability to conduct independent, high-level audits and articulate findings clearly.
- Excellent communication and technical writing skills.
Travel
- Must be willing and able to travel internationally, outside of North America, for the duration of the contract.
Interested?
If you're a former FDA inspector with OTC auditing experience and open to a global contract assignment from May-August 2026, we'd like to connect.
Additional Information
SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression and Indigenous status, or any other characteristics protected by law.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required.
This job description should not be construed as an exhaustive statement of duties, responsibilities, or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time.
Accommodations are available on request for qualified candidates during each stage of the recruitment process.
Please note that candidates applying for Canadian job openings should be authorized to work in Canada