Ensure compliance with ISO 13485| FDA 21 CFR Part 820| and Medtronic Supplier Quality requirements. Accurately document inspection results in quality records| travelers| and or electronic quality ...
Quick apply
Ensure compliance with ISO 13485| FDA 21 CFR Part 820| and Medtronic Supplier Quality requirements. Accurately document inspection results in quality records| travelers| and or electronic quality ...
Director, Head of Quality Management System CDx
Redmond, WA · On-site
$180 - $230/hr
FDA Inspection & Audit Readiness (Explicit Responsibility) * Serve as the primary quality contact for: * FDA inspections * Pre-approval inspections (PAI) * ISO audits and partner audits * Ensure ...
Director, Head of Quality Management System CDx
Redmond, WA · On-site
$180 - $230/hr
FDA Inspection & Audit Readiness (Explicit Responsibility) * Serve as the primary quality contact for: * FDA inspections * Pre-approval inspections (PAI) * ISO audits and partner audits * Ensure ...
Quality Inspector
Bridgeton, NJ · On-site
$18 - $21/hr
Support internal SQF audits and FDA/USDA inspection readiness by organizing records and ensuring documentation is complete and legible * Participate in corrective action and preventive action (CAPA ...
Quick apply
Quality Inspector
Bridgeton, NJ · On-site
$18 - $21/hr
Support internal SQF audits and FDA/USDA inspection readiness by organizing records and ensuring documentation is complete and legible * Participate in corrective action and preventive action (CAPA ...
Adhere to FDA and ISO requirements, safety guidelines, and corporate policies in all inspection activities. * Use measurement and test equipment such as calipers, optical comparators, and electronic ...
Quick apply
Adhere to FDA and ISO requirements, safety guidelines, and corporate policies in all inspection activities. * Use measurement and test equipment such as calipers, optical comparators, and electronic ...
Adhere to FDA and ISO requirements, safety guidelines, and corporate policies in all inspection activities. * Use measurement and test equipment such as calipers, optical comparators, and electronic ...
Quick apply
Adhere to FDA and ISO requirements, safety guidelines, and corporate policies in all inspection activities. * Use measurement and test equipment such as calipers, optical comparators, and electronic ...
Quality Inspector
Bridgeton, NJ · On-site
$18 - $21/hr
Support internal SQF audits and FDA/USDA inspection readiness by organizing records and ensuring documentation is complete and legible * Participate in corrective action and preventive action (CAPA ...
Quick apply
Quality Inspector
Bridgeton, NJ · On-site
$18 - $21/hr
Support internal SQF audits and FDA/USDA inspection readiness by organizing records and ensuring documentation is complete and legible * Participate in corrective action and preventive action (CAPA ...
Director, Head of Quality Management System CDx
Redmond, WA · On-site
$180K - $230K/yr
FDA Inspection & Audit Readiness (Explicit Responsibility) * Serve as the primary quality contact for: * FDA inspections * Pre-approval inspections (PAI) * ISO audits and partner audits * Ensure ...
Director, Head of Quality Management System CDx
Redmond, WA · On-site
$180K - $230K/yr
FDA Inspection & Audit Readiness (Explicit Responsibility) * Serve as the primary quality contact for: * FDA inspections * Pre-approval inspections (PAI) * ISO audits and partner audits * Ensure ...
Director, Head of Quality Management System CDx
Redmond, WA · On-site
$180K - $230K/yr
FDA Inspection & Audit Readiness (Explicit Responsibility) * Serve as the primary quality contact for: * FDA inspections * Pre-approval inspections (PAI) * ISO audits and partner audits * Ensure ...
Quick apply
Director, Head of Quality Management System CDx
Redmond, WA · On-site
$180K - $230K/yr
FDA Inspection & Audit Readiness (Explicit Responsibility) * Serve as the primary quality contact for: * FDA inspections * Pre-approval inspections (PAI) * ISO audits and partner audits * Ensure ...
... FDA regulations, and current Good Manufacturing Practices (cGMP). This role supports production and packaging operations while maintaining accurate documentation, ensuring product quality, and ...
... FDA regulations, and current Good Manufacturing Practices (cGMP). This role supports production and packaging operations while maintaining accurate documentation, ensuring product quality, and ...
Quality Inspector
Bridgeton, NJ · On-site
$18 - $21/hr
Support internal SQF audits and FDA/USDA inspection readiness by organizing records and ensuring documentation is complete and legible * Participate in corrective action and preventive action (CAPA ...
Quick apply
Quality Inspector
Bridgeton, NJ · On-site
$18 - $21/hr
Support internal SQF audits and FDA/USDA inspection readiness by organizing records and ensuring documentation is complete and legible * Participate in corrective action and preventive action (CAPA ...
Quality Inspector
Skaneateles, NY · On-site
As a Quality Inspector you are unafraid of navigating through necessary internal processes to ... Must be familiar with cGMP and FDA requirements. * Knowledge of aseptic techniques preferred.
Quality Inspector
Skaneateles, NY · On-site
As a Quality Inspector you are unafraid of navigating through necessary internal processes to ... Must be familiar with cGMP and FDA requirements. * Knowledge of aseptic techniques preferred.
As a Quality Inspector you are unafraid of navigating through necessary internal processes to ... Must be familiar with cGMP and FDA requirements. * Knowledge of aseptic techniques preferred.
As a Quality Inspector you are unafraid of navigating through necessary internal processes to ... Must be familiar with cGMP and FDA requirements. * Knowledge of aseptic techniques preferred.
Food Safety & GMP Quality Assurance Consultant Part time (Remote)
$62.50 - $76.50/hr
Support clients during FDA inspections, customer audits, certification audits, and regulatory responses. * Investigate quality events, complaints, deviations, nonconformances, and food safety ...
Food Safety & GMP Quality Assurance Consultant Part time (Remote)
$62.50 - $76.50/hr
Support clients during FDA inspections, customer audits, certification audits, and regulatory responses. * Investigate quality events, complaints, deviations, nonconformances, and food safety ...
... FDA regulations, and current Good Manufacturing Practices (cGMP). This role supports production and packaging operations while maintaining accurate documentation, ensuring product quality, and ...
... FDA regulations, and current Good Manufacturing Practices (cGMP). This role supports production and packaging operations while maintaining accurate documentation, ensuring product quality, and ...
Be Seen First
Production Associate | FDA
Sterling Heights, MI · On-site
$16 - $18/hr
Assembly employees are responsible for products made under FDA, MDARD, or USDA Inspection. Daily tasks will include: scrubbing, sanitizing, weighing, cutting, portioning, assembly and preparing ...
Quick apply
Be Seen First
Production Associate | FDA
Sterling Heights, MI · On-site
$16 - $18/hr
Assembly employees are responsible for products made under FDA, MDARD, or USDA Inspection. Daily tasks will include: scrubbing, sanitizing, weighing, cutting, portioning, assembly and preparing ...
Completes all required quality inspections following inspection instructions and/or product ... Knowledge of ISO, FDA and QSR concepts and guidelines preferred. Excellent communication and ...
Completes all required quality inspections following inspection instructions and/or product ... Knowledge of ISO, FDA and QSR concepts and guidelines preferred. Excellent communication and ...
... FDA regulations, and current Good Manufacturing Practices (cGMP). This role supports production and packaging operations while maintaining accurate documentation, ensuring product quality, and ...
... FDA regulations, and current Good Manufacturing Practices (cGMP). This role supports production and packaging operations while maintaining accurate documentation, ensuring product quality, and ...
Minimum 3 years of experience in Quality Inspection (or minimum 6 Yrs in a manufacturing environment where responsible for measurement of products) and preferably in an FDA regulated environment ...
Minimum 3 years of experience in Quality Inspection (or minimum 6 Yrs in a manufacturing environment where responsible for measurement of products) and preferably in an FDA regulated environment ...
Quality Inspector
Clackamas, OR · On-site
Pay Rate Low: 20 | Pay Rate High: 22 Quality Inspector Location: Fully Onsite - Clackamas, OR ... Experience with FDA/cGMP compliance * Hands-on experience with non-conformances, OOS investigations ...
Quality Inspector
Clackamas, OR · On-site
Pay Rate Low: 20 | Pay Rate High: 22 Quality Inspector Location: Fully Onsite - Clackamas, OR ... Experience with FDA/cGMP compliance * Hands-on experience with non-conformances, OOS investigations ...
In the near term, the work centers on FDA inspection readiness and maintaining QMS and GxP compliance across sponsor, CRO, and clinical site operations.Usona's team is small, close knit, and deeply ...
In the near term, the work centers on FDA inspection readiness and maintaining QMS and GxP compliance across sponsor, CRO, and clinical site operations.Usona's team is small, close knit, and deeply ...
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?
As of Aug 24, 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 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.
What skills and qualifications are needed to be an FDA inspector?
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 types of facilities or products do FDA inspectors 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.
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 related areas. They must pass a written exam and a background check, and often undergo specialized training at the FDA's training center. Certification or licensing is not required but can enhance prospects in the field.
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Cities with the most Fda Inspector job openings:
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The most popular types of Fda Inspector jobs are:
What states have the most Fda Inspector jobs?
States with the most job openings for Fda Inspector jobs include:
What job categories do people searching Fda Inspector jobs look for?
The top searched job categories for Fda Inspector jobs are:
Contractor
Re-posted 19 days ago
Job description
Role : QC inspector/ Quality Control Inspector
Location: El Paso, TX
Duration: 6 months
Looking for someone with 3-5 years of Experience
Description : Must Have Technical Functional Skills Perform incoming| in process| and final inspections of components| sub-assemblies| and or finished goods in accordance with approved inspection plans| drawings| and specifications. Conduct inspections using visual| dimensional| and functional methods| utilizing calibrated measurement tools such as calipers| micrometers| and gauges. Ensure compliance with ISO 13485| FDA 21 CFR Part 820| and Medtronic Supplier Quality requirements. Accurately document inspection results in quality records| travelers| and or electronic quality systems in accordance with Good Documentation Practices (GDP).Identify| document| and escalate nonconforming material| supporting containment actions and investigations. Support lot release activities and ensure full traceability of inspected materials. Participate in root cause analysis| CAPA activities| and continuous improvement initiatives as required. Support readiness for internal| customer| and regulatory audits. Collaborate with Manufacturing| Engineering| and Supplier Quality teams to resolve quality issues in a timely manner Roles Responsibilities Perform incoming| in process| and final inspections of components| sub-assemblies| and or finished goods in accordance with approved inspection plans| drawings| and specifications .Conduct inspections using visual| dimensional| and functional methods| utilizing calibrated measurement tools such as calipers| micrometers| and gauges. Ensure compliance with ISO 13485| FDA 21 CFR Part 820| Accurately document inspection results in quality records| travelers| and or electronic quality systems in accordance with Good Documentation Practices (GDP).Identify| document| and escalate nonconforming material| supporting containment actions and investigations .Support lot release activities and ensure full traceability of inspected materials. Participate in root cause analysis| CAPA activities| and continuous improvement initiatives as required. Support readiness for internal| customer| and regulatory audits. Collaborate with Manufacturing| Engineering
About Siri Infosolutions
Sourced by ZipRecruiter
Our team of experts first gather each and every requirement of yours. Our research and development team then sit around those requirements and come up with a plan. Our implementation team then executes that plan for optimal results. After that our support team remains in constant touch with you during and after the entire process.
Industry
It services
Company size
201 - 500 Employees
Headquarters location
Edison, NJ, US
Year founded
2005