Conduct quality audits in accordance with ISO 13485, ISO 9001, and FDA regulations to ensure compliance with industry standards and regulatory requirements. * Document inspection results meticulously ...
Conduct quality audits in accordance with ISO 13485, ISO 9001, and FDA regulations to ensure compliance with industry standards and regulatory requirements. * Document inspection results meticulously ...
Quality Inspector - First Shift
Manteno, IL · On-site
$24/hr
Conduct quality audits in accordance with ISO 13485, ISO 9001, and FDA regulations to ensure compliance with industry standards and regulatory requirements. * Document inspection results meticulously ...
Quality Inspector - First Shift
Manteno, IL · On-site
$24/hr
Conduct quality audits in accordance with ISO 13485, ISO 9001, and FDA regulations to ensure compliance with industry standards and regulatory requirements. * Document inspection results meticulously ...
Support regulatory inspections, audits, and inquiries related to post-market surveillance and adverse event reporting. Knowledge, Skills & Abilities * Strong understanding of FDA regulatory ...
Support regulatory inspections, audits, and inquiries related to post-market surveillance and adverse event reporting. Knowledge, Skills & Abilities * Strong understanding of FDA regulatory ...
Regulatory Affairs Manager
Niles, IL · On-site
Support regulatory inspections, audits, and inquiries related to post-market surveillance and adverse event reporting. Knowledge, Skills & Abilities * Strong understanding of FDA regulatory ...
Regulatory Affairs Manager
Niles, IL · On-site
Support regulatory inspections, audits, and inquiries related to post-market surveillance and adverse event reporting. Knowledge, Skills & Abilities * Strong understanding of FDA regulatory ...
Lead and support internal audits, external audits, inspections, and regulatory assessments, including FDA, UL, ISO 13485, customer, corporate, and notified body audits. * Contribute to Management ...
Lead and support internal audits, external audits, inspections, and regulatory assessments, including FDA, UL, ISO 13485, customer, corporate, and notified body audits. * Contribute to Management ...
Lead and support internal audits, external audits, inspections, and regulatory assessments, including FDA, UL, ISO 13485, customer, corporate, and notified body audits. * Contribute to Management ...
Lead and support internal audits, external audits, inspections, and regulatory assessments, including FDA, UL, ISO 13485, customer, corporate, and notified body audits. * Contribute to Management ...
Working knowledge of quality systems including ISO 9001, ISO 13485, HACCP, FDA regulations, and ... vision inspection systems, and coordinate measuring machines (CMM). * Demonstrated ability to ...
Working knowledge of quality systems including ISO 9001, ISO 13485, HACCP, FDA regulations, and ... vision inspection systems, and coordinate measuring machines (CMM). * Demonstrated ability to ...
DDT Medical Device Investigation Analyst
Bannockburn, IL · On-site
$89K - $141K/yr
Execute FDA-ready investigations proportional to complaint significance, producing complete, defensible, inspection-ready records. * Reproduce defects in qualified environments and analyzed ...
DDT Medical Device Investigation Analyst
Bannockburn, IL · On-site
$89K - $141K/yr
Execute FDA-ready investigations proportional to complaint significance, producing complete, defensible, inspection-ready records. * Reproduce defects in qualified environments and analyzed ...
DDT Medical Device Investigation Analyst
Bannockburn, IL · On-site
$89K - $141K/yr
Execute FDA-ready investigations proportional to complaint significance, producing complete, defensible, inspection-ready records. * Reproduce defects in qualified environments and analyzed ...
DDT Medical Device Investigation Analyst
Bannockburn, IL · On-site
$89K - $141K/yr
Execute FDA-ready investigations proportional to complaint significance, producing complete, defensible, inspection-ready records. * Reproduce defects in qualified environments and analyzed ...
Quality Assurance Manager
Itasca, IL · On-site
... inspections, and quality-related regulatory interactions Key Responsibilities ● Develop, implement, and maintain the QMS in compliance with FDA 21 CFR Part 820, ISO 13485, ISO 14971, and other ...
Quick apply
Quality Assurance Manager
Itasca, IL · On-site
... inspections, and quality-related regulatory interactions Key Responsibilities ● Develop, implement, and maintain the QMS in compliance with FDA 21 CFR Part 820, ISO 13485, ISO 14971, and other ...
Quality Assurance Manager
Itasca, IL · On-site
... inspections, and quality-related regulatory interactions Key Responsibilities ● Develop, implement, and maintain the QMS in compliance with FDA 21 CFR Part 820, ISO 13485, ISO 14971, and other ...
Quick apply
Quality Assurance Manager
Itasca, IL · On-site
... inspections, and quality-related regulatory interactions Key Responsibilities ● Develop, implement, and maintain the QMS in compliance with FDA 21 CFR Part 820, ISO 13485, ISO 14971, and other ...
Quality Assurance Manager
Itasca, IL · On-site
... inspections, and quality-related regulatory interactions Key Responsibilities ● Develop, implement, and maintain the QMS in compliance with FDA 21 CFR Part 820, ISO 13485, ISO 14971, and other ...
Quick apply
Quality Assurance Manager
Itasca, IL · On-site
... inspections, and quality-related regulatory interactions Key Responsibilities ● Develop, implement, and maintain the QMS in compliance with FDA 21 CFR Part 820, ISO 13485, ISO 14971, and other ...
Quality Assurance Manager
Itasca, IL · On-site
... inspections, and quality-related regulatory interactions Key Responsibilities ● Develop, implement, and maintain the QMS in compliance with FDA 21 CFR Part 820, ISO 13485, ISO 14971, and other ...
Quick apply
Quality Assurance Manager
Itasca, IL · On-site
... inspections, and quality-related regulatory interactions Key Responsibilities ● Develop, implement, and maintain the QMS in compliance with FDA 21 CFR Part 820, ISO 13485, ISO 14971, and other ...
Quality Assurance Manager
Itasca, IL · On-site
... inspections, and quality-related regulatory interactions Key Responsibilities ● Develop, implement, and maintain the QMS in compliance with FDA 21 CFR Part 820, ISO 13485, ISO 14971, and other ...
Quick apply
Quality Assurance Manager
Itasca, IL · On-site
... inspections, and quality-related regulatory interactions Key Responsibilities ● Develop, implement, and maintain the QMS in compliance with FDA 21 CFR Part 820, ISO 13485, ISO 14971, and other ...
Quality Assurance Manager
Itasca, IL · On-site
... inspections, and quality-related regulatory interactions Key Responsibilities ● Develop, implement, and maintain the QMS in compliance with FDA 21 CFR Part 820, ISO 13485, ISO 14971, and other ...
Quick apply
Quality Assurance Manager
Itasca, IL · On-site
... inspections, and quality-related regulatory interactions Key Responsibilities ● Develop, implement, and maintain the QMS in compliance with FDA 21 CFR Part 820, ISO 13485, ISO 14971, and other ...
Quality Assurance Manager
Itasca, IL · On-site
... inspections, and quality-related regulatory interactions Key Responsibilities ● Develop, implement, and maintain the QMS in compliance with FDA 21 CFR Part 820, ISO 13485, ISO 14971, and other ...
Quick apply
Quality Assurance Manager
Itasca, IL · On-site
... inspections, and quality-related regulatory interactions Key Responsibilities ● Develop, implement, and maintain the QMS in compliance with FDA 21 CFR Part 820, ISO 13485, ISO 14971, and other ...
Quality Assurance Manager
Itasca, IL · On-site
... inspections, and quality-related regulatory interactions Key Responsibilities ● Develop, implement, and maintain the QMS in compliance with FDA 21 CFR Part 820, ISO 13485, ISO 14971, and other ...
Quick apply
Quality Assurance Manager
Itasca, IL · On-site
... inspections, and quality-related regulatory interactions Key Responsibilities ● Develop, implement, and maintain the QMS in compliance with FDA 21 CFR Part 820, ISO 13485, ISO 14971, and other ...
Quality Assurance Manager
Itasca, IL · On-site
... inspections, and quality-related regulatory interactions Key Responsibilities ● Develop, implement, and maintain the QMS in compliance with FDA 21 CFR Part 820, ISO 13485, ISO 14971, and other ...
Quick apply
Quality Assurance Manager
Itasca, IL · On-site
... inspections, and quality-related regulatory interactions Key Responsibilities ● Develop, implement, and maintain the QMS in compliance with FDA 21 CFR Part 820, ISO 13485, ISO 14971, and other ...
Validation Engineer
$85K/yr
Support FDA inspection readiness activities. * Interfacing customers, staff and fellow managers to establish and maintain validation schedules throughout the company. * Ability to interact with ...
Validation Engineer
$85K/yr
Support FDA inspection readiness activities. * Interfacing customers, staff and fellow managers to establish and maintain validation schedules throughout the company. * Ability to interact with ...
Inspect raw materials, production processes, and finished products to ensure quality standards are met * Monitor production operations to maintain compliance with company, GMP, HACCP, USDA, and FDA ...
Quick apply
Inspect raw materials, production processes, and finished products to ensure quality standards are met * Monitor production operations to maintain compliance with company, GMP, HACCP, USDA, and FDA ...
Fda Inspector information
See Illinois salary details
$23.7K - $30.3K
3% of jobs
$30.3K - $36.9K
16% of jobs
$38.5K is the 25th percentile. Wages below this are outliers.
$36.9K - $43.4K
23% of jobs
The median wage is $45.4K / yr.
$43.4K - $50K
27% of jobs
$54.2K is the 75th percentile. Wages above this are outliers.
$50K - $56.6K
10% of jobs
$56.6K - $63.1K
4% of jobs
$63.1K - $69.7K
5% of jobs
$69.7K - $76.2K
2% of jobs
$76.2K - $82.8K
2% of jobs
$82.8K - $89.4K
2% of jobs
$89.4K - $95.9K
5% of jobs
$23.7K
$53.2K
$95.9K
How much do fda inspector jobs pay per year?
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?
What are the most commonly searched types of Fda Inspector jobs in Illinois?
The most popular types of Fda Inspector jobs in Illinois are:
What are popular job titles related to Fda Inspector jobs in Illinois?
For Fda Inspector jobs in Illinois, the most frequently searched job titles are:
What job categories do people searching Fda Inspector jobs in Illinois look for?
The top searched job categories for Fda Inspector jobs in Illinois are:
What cities in Illinois are hiring for Fda Inspector jobs?
Cities in Illinois with the most Fda Inspector job openings:

Quality Inspector - First Shift
Manteno, IL
Other
Re-posted 22 days ago
Job description
Job Overview
We are seeking a detail-oriented and energetic Quality Inspector to join our team on the First Shift. In this pivotal role, you will ensure that all manufactured products meet strict quality standards and comply with industry regulations. Your keen eye for detail, combined with your expertise in quality systems and measurement tools, will help maintain our commitment to excellence. This position offers an exciting opportunity to contribute to high-quality manufacturing processes in a fast-paced environment, supporting continuous improvement and customer satisfaction.
Duties
- Perform thorough inspections of products using precision measuring instruments such as calipers, micrometers, and vision inspection systems to verify conformance to specifications.
- Utilize advanced quality management tools like Calypso and coordinate measuring machines (CMM) to gather accurate data during inspections.
- Conduct quality audits in accordance with ISO 13485, ISO 9001, and FDA regulations to ensure compliance with industry standards and regulatory requirements.
- Document inspection results meticulously, including data collection and analysis, to support quality assurance initiatives.
- Identify non-conformances and collaborate with manufacturing teams to implement corrective actions aligned with CGMP (Current Good Manufacturing Practice) and HACCP protocols.
- Participate in root cause analysis and problem-solving activities to improve product quality and process efficiency.
- Support internal and external quality audits by providing detailed reports and maintaining comprehensive records of inspection activities.
Experience
- Proven experience in manufacturing quality control or inspection roles within regulated industries such as medical devices or food production.
- Strong knowledge of quality systems including ISO 9001, ISO 13485, HACCP, FDA regulations, and CGMP standards.
- Hands-on experience operating precision measurement instruments like calipers, micrometers, vision inspection systems, and coordinate measuring machines (CMM).
- Familiarity with quality management software such as Calypso is highly desirable.
- Demonstrated ability to analyze data accurately, identify trends, and recommend process improvements.
- Excellent attention to detail combined with strong communication skills for clear documentation and reporting.
- Ability to work effectively during second shift hours in a dynamic environment committed to continuous improvement. Join us as a Quality Inspector on the Second Shift and play a vital role in delivering products that meet the highest standards of safety, quality, and reliability!
About Gotion
Sourced by ZipRecruiter
Industry
Manufacturing
Company size
1 - 10 Employees
Headquarters location
Fremont, CA, US
Year founded
2014