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 Manager
Monroe, OH · On-site
Experience with FDA or ISO quality standards, including several completed ISO audits and FDA inspections. * 5 plus years' experience in Quality System and Compliance environment with at least 5 years ...
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Quality Manager
Monroe, OH · On-site
Experience with FDA or ISO quality standards, including several completed ISO audits and FDA inspections. * 5 plus years' experience in Quality System and Compliance environment with at least 5 years ...
Ensure compliance with FDA GMPs and company quality systems. * Keep work areas clean, organized, and ready for inspection. * Follow and promote kdc/one's safety and environmental policies. * Complete ...
Ensure compliance with FDA GMPs and company quality systems. * Keep work areas clean, organized, and ready for inspection. * Follow and promote kdc/one's safety and environmental policies. * Complete ...
Ensure compliance with FDA GMPs and company quality systems. * Keep work areas clean, organized, and ready for inspection. * Follow and promote kdc/one's safety and environmental policies. * Complete ...
Ensure compliance with FDA GMPs and company quality systems. * Keep work areas clean, organized, and ready for inspection. * Follow and promote kdc/one's safety and environmental policies. * Complete ...
Ensure compliance with FDA GMPs and company quality systems. * Keep work areas clean, organized, and ready for inspection. * Follow and promote kdc/one's safety and environmental policies. * Complete ...
Ensure compliance with FDA GMPs and company quality systems. * Keep work areas clean, organized, and ready for inspection. * Follow and promote kdc/one's safety and environmental policies. * Complete ...
Ensure compliance with FDA GMPs and company quality systems. * Keep work areas clean, organized, and ready for inspection. * Follow and promote kdc/one's safety and environmental policies. * Complete ...
Ensure compliance with FDA GMPs and company quality systems. * Keep work areas clean, organized, and ready for inspection. * Follow and promote kdc/one's safety and environmental policies. * Complete ...
Ensure compliance with FDA GMPs and company quality systems. * Keep work areas clean, organized, and ready for inspection. * Follow and promote kdc/one's safety and environmental policies. * Complete ...
Ensure compliance with FDA GMPs and company quality systems. * Keep work areas clean, organized, and ready for inspection. * Follow and promote kdc/one's safety and environmental policies. * Complete ...
Ensure compliance with FDA GMPs and company quality systems. * Keep work areas clean, organized, and ready for inspection. * Follow and promote kdc/one's safety and environmental policies. * Complete ...
Ensure compliance with FDA GMPs and company quality systems. * Keep work areas clean, organized, and ready for inspection. * Follow and promote kdc/one's safety and environmental policies. * Complete ...
Receipt Inspector
Cincinnati, OH · On-site
Ensure compliance with FDA, USDA, and company food safety requirements as applicable. * Maintain cleanliness and organization of inspection areas. Documentation & Computer Use * Accurately complete ...
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Receipt Inspector
Cincinnati, OH · On-site
Ensure compliance with FDA, USDA, and company food safety requirements as applicable. * Maintain cleanliness and organization of inspection areas. Documentation & Computer Use * Accurately complete ...
Quality Inspector
Cleveland, OH · On-site
$28 - $32/hr
Our FDA 510(k)-cleared Dreem EEG headband and AI algorithms enable quantitative biomarker discovery ... We are looking for a detail-oriented, quality-focused Quality Inspector to join our Cleveland team.
Quality Inspector
Cleveland, OH · On-site
$28 - $32/hr
Our FDA 510(k)-cleared Dreem EEG headband and AI algorithms enable quantitative biomarker discovery ... We are looking for a detail-oriented, quality-focused Quality Inspector to join our Cleveland team.
Quality Inspector
$28 - $32/hr
Our FDA 510(k)-cleared Dreem EEG headband and AI algorithms enable quantitative biomarker discovery ... We are looking for a detail-oriented, quality-focused Quality Inspector to join our Cleveland team.
Quality Inspector
$28 - $32/hr
Our FDA 510(k)-cleared Dreem EEG headband and AI algorithms enable quantitative biomarker discovery ... We are looking for a detail-oriented, quality-focused Quality Inspector to join our Cleveland team.
Product Quality Inspector
Cleveland, OH · On-site
Experience with ISO and FDA audits * Experience with QC/QA medical device inspection or test, especially MRI Skills and Abilities Required * Meticulous attention to detail - absolute must * Must be ...
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Product Quality Inspector
Cleveland, OH · On-site
Experience with ISO and FDA audits * Experience with QC/QA medical device inspection or test, especially MRI Skills and Abilities Required * Meticulous attention to detail - absolute must * Must be ...
Product Quality Inspector
Cleveland, OH · On-site
Experience with ISO and FDA audits * Experience with QC/QA medical device inspection or test, especially MRI Skills and Abilities Required * Meticulous attention to detail - absolute must * Must be ...
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Product Quality Inspector
Cleveland, OH · On-site
Experience with ISO and FDA audits * Experience with QC/QA medical device inspection or test, especially MRI Skills and Abilities Required * Meticulous attention to detail - absolute must * Must be ...
Senior Quality Control & Compliance Engineer
$85K - $100K/yr
Support FDA compliance activities for medical device production * Lead internal audits, customer audits, and third-party certification audits while assisting with preparation for FDA inspections
New
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Senior Quality Control & Compliance Engineer
$85K - $100K/yr
Support FDA compliance activities for medical device production * Lead internal audits, customer audits, and third-party certification audits while assisting with preparation for FDA inspections
New
As a Quality Assurance Inspector, you'll be ensuring our products meet our high standards from ... Maintain compliance with FDA GMP regulations and company quality systems. * Perform other duties as ...
As a Quality Assurance Inspector, you'll be ensuring our products meet our high standards from ... Maintain compliance with FDA GMP regulations and company quality systems. * Perform other duties as ...
Food Safety & Quality Assurance (FSQA) Manager
Cincinnati, OH · On-site
$115K - $130K/yr
Serve as the primary liaison for USDA/FDA inspections, customer audits, and regulatory agencies. Ensure accurate product labeling and compliance with customer specifications. Manage departmental ...
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Food Safety & Quality Assurance (FSQA) Manager
Cincinnati, OH · On-site
$115K - $130K/yr
Serve as the primary liaison for USDA/FDA inspections, customer audits, and regulatory agencies. Ensure accurate product labeling and compliance with customer specifications. Manage departmental ...
Incoming Inspector - Third Shift - kdc/one Columbus
New Albany, OH · On-site
$21/hr
Ensure compliance with FDA GMPs and company quality systems. * Keep work areas clean, organized, and ready for inspection. * Follow and promote kdc/one's safety and environmental policies. * Complete ...
Incoming Inspector - Third Shift - kdc/one Columbus
New Albany, OH · On-site
$21/hr
Ensure compliance with FDA GMPs and company quality systems. * Keep work areas clean, organized, and ready for inspection. * Follow and promote kdc/one's safety and environmental policies. * Complete ...
Quality Assurance Manager
Brilliant, OH · On-site
$60K/yr
Conduct and participate directly in quality inspections, internal and external audits, and FDA inspections. * Participate in CAPA systems. Prepare reports and corrective actions. * Maintain and ...
Quality Assurance Manager
Brilliant, OH · On-site
$60K/yr
Conduct and participate directly in quality inspections, internal and external audits, and FDA inspections. * Participate in CAPA systems. Prepare reports and corrective actions. * Maintain and ...
Ensure all maintenance activities comply with GMP, FDA, and site SOPs * Document maintenance work ... Basic understanding of PLC-based systems and serialization/vision inspection tools * Ability to ...
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Ensure all maintenance activities comply with GMP, FDA, and site SOPs * Document maintenance work ... Basic understanding of PLC-based systems and serialization/vision inspection tools * Ability to ...
Director, Quality Microbiology
$166K - $228K/yr
Participate as a microbiology SME in internal audits, and external audits such as FDA inspections, ISO certifications, surveillance audits and customer audits. * Maintain a strong working knowledge ...
Director, Quality Microbiology
$166K - $228K/yr
Participate as a microbiology SME in internal audits, and external audits such as FDA inspections, ISO certifications, surveillance audits and customer audits. * Maintain a strong working knowledge ...
Fda Inspector information
See Ohio salary details
$23.3K - $29.7K
3% of jobs
$29.7K - $36.2K
16% of jobs
$37.8K is the 25th percentile. Wages below this are outliers.
$36.2K - $42.6K
23% of jobs
The median wage is $44.5K / yr.
$42.6K - $49K
27% of jobs
$53.2K is the 75th percentile. Wages above this are outliers.
$49K - $55.5K
10% of jobs
$55.5K - $61.9K
4% of jobs
$61.9K - $68.4K
5% of jobs
$68.4K - $74.8K
2% of jobs
$74.8K - $81.2K
2% of jobs
$81.2K - $87.7K
2% of jobs
$87.7K - $94.1K
5% of jobs
$23.3K
$52.2K
$94.1K
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.

Job description
A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
Our Client is looking for Quality Inspector- With good experience in Quality, Inspections, documentations, guidelines etc. experience.....!!!!!
SUMMARY & RESPONSIBILITIES:Â
Completes all required quality inspections following inspection instructions and/or product drawings.Â
Use department databases to track and manage inspection workload and rejected products. Effectively follow SOPs, policies, and ISO/QSR requirements.Â
Completes archival activities for device history records for lots inspected.
Writes and processes Material Reject Reports, as necessary, and manage inventory that is on hold for quality inspection.Â
Reviews and updates inspection plans as needed. Write DCO's (Engineering Change Requests) to update as required. Assist Operations personnel in maintenance and updating of other Device Master Record documentation.Â
Provides support for the Quality System during corporate audits, actively participate in department activities and Perform audits of operations areas to confirm compliance with controlled procedures, as requiredÂ
QUALIFICATIONS AND SKILLS NEEDED:Â
A bachelor's degree or Master's degree in Science or with 1-5 years of experience in a pharmaceutical/biotechnology industry.
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
Ability to interpret instructions and drawings to effectively inspect product. Working knowledge of GD&T preferred.
Ability to utilize multiple gauges and measurement tools for inspection of manufactured components and assemblies.
Previous experience with CMM and/or Vision System operation is a plus.
Use of math skills relative to physical measurement of product (calculations involving basic functions and some geometry/trigonometry in English and metric units)
Knowledge of ISO, FDA and QSR concepts and guidelines preferred.
Excellent communication and organizational skills.
Outstanding attention to detail
Strong interpersonal skills and ability to work with others in a positive and collaborative manner.
Demonstrated ability to work accurately, follow instructions/schedules/timelines and handle multiple priorities.
Knowledge of various MS Office applications such as: Word, Excel, and Access.
Some overtime may be done
Regards
Pooja Mishra
Clinical Recruiter
Integrated Resources, Inc.Â
IT Life Sciences Allied Healthcare CRO
Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I
Tel: 732 429 1636
(W) 732-549-2030 x 214 | (F) 732-549-5549
Gold Seal JCAHO Certified for Health Care StaffingÂ
"INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES" (8th Year in a Row)
About Integrated Resources
Sourced by ZipRecruiter
Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.
Industry
Recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
Edison, NJ, US
Year founded
1996