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Fda Inspector Jobs (NOW HIRING)

Accord Technologies Inc.

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 ...

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The Rockridge Group

Be Seen First

Senior FDA Regulatory Attorney

New York, NY · Remote

$250K - $350K/yr

Counsel clients regarding FDA regulations, guidance, inspections, investigations, warning letters, and enforcement actions. * Provide guidance on: * Compounding (503A and 503B) * Drug Supply Chain ...

The Rockridge Group

Be Seen First

Senior FDA Regulatory Attorney

New York, NY · Remote

$250K - $350K/yr

Counsel clients regarding FDA regulations, guidance, inspections, investigations, warning letters, and enforcement actions. * Provide guidance on: * Compounding (503A and 503B) * Drug Supply Chain ...

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The Rockridge Group

FDA Attorney

Pine Brook, NJ · On-site +1

... FDA inspections, 483 responses and warning letters • Drug withdrawals and recalls • FDA importation and exportation rules • Veterinary medicine and veterinary compounding • Dietary ...

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Alston

FDA Technical Consultant

Washington, DC · On-site +1

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 ...

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Fda Inspector information

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$24.5K

$54.9K

$99K

How much do fda inspector jobs pay per year?

As of Jun 30, 2026, the average yearly pay for fda inspector in the United States is $54,939.00, according to ZipRecruiter salary data. Most workers in this role earn between $38,500.00 and $63,500.00 per year, depending on experience, location, and employer.

What type of inspectors make the most money?

Within the FDA inspection roles, senior-level inspectors such as Supervisory Food and Drug Inspectors or those with specialized expertise in areas like pharmaceuticals or biotechnology tend to earn higher salaries. Factors influencing pay include experience, certifications, and the complexity of inspections conducted, often requiring advanced knowledge of regulations and compliance standards.

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 are the four types of FDA Inspections?

FDA inspectors conduct four main types of inspections: routine inspections to monitor compliance, for-cause inspections triggered by specific concerns or complaints, follow-up inspections to verify corrective actions, and pre-approval inspections for new drug or device applications. These inspections help ensure that facilities meet regulatory standards for safety and quality.

Is it hard to get a job at FDA?

Becoming an FDA inspector can be competitive due to strict qualification requirements, including relevant experience, education, and passing civil service exams. Candidates often need a background in science, public health, or regulatory fields, along with strong attention to detail and knowledge of FDA regulations. The hiring process can be lengthy and involves multiple steps such as interviews and background checks.

How do you become an FDA inspector?

To become an FDA inspector, candidates typically need a bachelor's degree in a relevant field such as biology, chemistry, or food science, along with experience in food safety, pharmaceuticals, or manufacturing. They must pass a written exam and a background check, and often complete training at the FDA's training center. Strong attention to detail, knowledge of regulatory standards, and good communication skills are essential for the role.

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.

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Fda Inspector jobs near you

Subcontractor - Senior OTC Compliance Auditor (Great opportunity for former FDA Inspectors)

SGS U.S. Holding Inc.

Remote

Full-time

Posted 26 days ago

Job description

Company 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, highlevel 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

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