Maintains all QA documents necessary to exceed Annual FDA Inspection requirements. * Is responsible for obtaining and maintaining ACR accreditation. Exceptional compensation for the right candidate!
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Maintains all QA documents necessary to exceed Annual FDA Inspection requirements. * Is responsible for obtaining and maintaining ACR accreditation. Exceptional compensation for the right candidate!
Quick apply
Maintains all QA documents necessary to exceed Annual FDA Inspection requirements. * Is responsible for obtaining and maintaining ACR accreditation. Exceptional compensation for the right candidate!
Ensure IT systems comply with GxP, FDA 21 CFR Part 11, and data integrity requirements. Participate ... Support audits and inspections as needed. Required Qualifications Bachelor's degree in Computer ...
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Ensure IT systems comply with GxP, FDA 21 CFR Part 11, and data integrity requirements. Participate ... Support audits and inspections as needed. Required Qualifications Bachelor's degree in Computer ...
Richardson, TX · On-site
Coordinate environmental compliance programs, inspections, audits, and regulatory reporting ... Knowledge of OSHA, EPA, FDA, EMA, cGMP, and applicable environmental and safety regulations.
Richardson, TX · On-site
Coordinate environmental compliance programs, inspections, audits, and regulatory reporting ... Knowledge of OSHA, EPA, FDA, EMA, cGMP, and applicable environmental and safety regulations.
Coordinate environmental compliance programs, inspections, audits, and regulatory reporting ... Knowledge of OSHA, EPA, FDA, EMA, cGMP, and applicable environmental and safety regulations.
Coordinate environmental compliance programs, inspections, audits, and regulatory reporting ... Knowledge of OSHA, EPA, FDA, EMA, cGMP, and applicable environmental and safety regulations.
... inspections Requirements: * Prior experience in quality control, food safety, or a related role in a manufacturing or packaging environment * Working knowledge of HACCP, GMP, FDA regulations, and ...
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... inspections Requirements: * Prior experience in quality control, food safety, or a related role in a manufacturing or packaging environment * Working knowledge of HACCP, GMP, FDA regulations, and ...
... inspections Requirements: * Prior experience in quality control, food safety, or a related role in a manufacturing or packaging environment * Working knowledge of HACCP, GMP, FDA regulations, and ...
Quick apply
... inspections Requirements: * Prior experience in quality control, food safety, or a related role in a manufacturing or packaging environment * Working knowledge of HACCP, GMP, FDA regulations, and ...
... inspections Requirements: * Prior experience in quality control, food safety, or a related role in a manufacturing or packaging environment * Working knowledge of HACCP, GMP, FDA regulations, and ...
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... inspections Requirements: * Prior experience in quality control, food safety, or a related role in a manufacturing or packaging environment * Working knowledge of HACCP, GMP, FDA regulations, and ...
Ensure all investigations comply with FDA guidance, cGMPs, and expectations for sterile drug ... Support audit readiness and provide SME support during regulatory inspections as needed. Retest and ...
Ensure all investigations comply with FDA guidance, cGMPs, and expectations for sterile drug ... Support audit readiness and provide SME support during regulatory inspections as needed. Retest and ...
Responsible for annual inspection by TDH and FDA. Attend monthly departmental staff meetings. Responsible for completing quarterly QI report for QRMC. Non-Direct Patient Care: * Documentation:
Responsible for annual inspection by TDH and FDA. Attend monthly departmental staff meetings. Responsible for completing quarterly QI report for QRMC. Non-Direct Patient Care: * Documentation:
Fort Worth, TX · On-site
Responsible for annual inspection by TDH and FDA. Attend monthly departmental staff meetings. Responsible for completing quarterly QI report for QRMC. Non-Direct Patient Care: * Documentation:
Fort Worth, TX · On-site
Responsible for annual inspection by TDH and FDA. Attend monthly departmental staff meetings. Responsible for completing quarterly QI report for QRMC. Non-Direct Patient Care: * Documentation:
Responsible for annual inspection by TDH and FDA. Attend monthly departmental staff meetings. Responsible for completing quarterly QI report for QRMC. Non Direct Patient Care: * Documentation:
Responsible for annual inspection by TDH and FDA. Attend monthly departmental staff meetings. Responsible for completing quarterly QI report for QRMC. Non Direct Patient Care: * Documentation:
FDA, ISO, etc.) and actively participate and represent the company in 3rd party inspections. Maintain up-to-date knowledge, identify, and monitor applicable standards and guidance documents for ...
FDA, ISO, etc.) and actively participate and represent the company in 3rd party inspections. Maintain up-to-date knowledge, identify, and monitor applicable standards and guidance documents for ...
... for FDA * Technical documentation for EU MDR compliance * International product registration ... Audits and Inspections: * Support and participate in internal and external audits and regulatory ...
... for FDA * Technical documentation for EU MDR compliance * International product registration ... Audits and Inspections: * Support and participate in internal and external audits and regulatory ...
Burleson, TX · On-site
$16 - $20.50/hr
Inspect incoming product for damage, labeling accuracy, lot codes, and compliance requirements * Accurately record receipts in the inventory management system following FDA and internal traceability ...
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Burleson, TX · On-site
$16 - $20.50/hr
Inspect incoming product for damage, labeling accuracy, lot codes, and compliance requirements * Accurately record receipts in the inventory management system following FDA and internal traceability ...
... for FDA * Technical documentation for EU MDR compliance * International product registration ... Audits and Inspections: * Support and participate in internal and external audits and regulatory ...
... for FDA * Technical documentation for EU MDR compliance * International product registration ... Audits and Inspections: * Support and participate in internal and external audits and regulatory ...
... submissions for FDA Technical documentation for EU MDR compliance International product ... Support and participate in internal and external audits and regulatory agency inspections QMS ...
... submissions for FDA Technical documentation for EU MDR compliance International product ... Support and participate in internal and external audits and regulatory agency inspections QMS ...
FDA, ISO, etc.) and actively participate and represent the company in 3rd party inspections. • Maintain up-to-date knowledge, identify, and monitor applicable standards and guidance documents for ...
FDA, ISO, etc.) and actively participate and represent the company in 3rd party inspections. • Maintain up-to-date knowledge, identify, and monitor applicable standards and guidance documents for ...
Irving, TX · On-site
$17/hr
Inspect components and finished products for compliance with FDA and ISO standards. * Troubleshoot production issues and collaborate with engineering, quality, and product development teams.
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Irving, TX · On-site
$17/hr
Inspect components and finished products for compliance with FDA and ISO standards. * Troubleshoot production issues and collaborate with engineering, quality, and product development teams.
OSHA, ISO 9001 EPA, FDA, TTB and DOT. Identify best practices and lead continuous improvement ... Performs safety surveys and inspections, prepares written reports of findings and recommendations ...
OSHA, ISO 9001 EPA, FDA, TTB and DOT. Identify best practices and lead continuous improvement ... Performs safety surveys and inspections, prepares written reports of findings and recommendations ...
Irving, TX · On-site
$17/hr
Inspect components and finished products for compliance with FDA and ISO standards. * Troubleshoot production issues and collaborate with engineering, quality, and product development teams.
Quick apply
Irving, TX · On-site
$17/hr
Inspect components and finished products for compliance with FDA and ISO standards. * Troubleshoot production issues and collaborate with engineering, quality, and product development teams.
$24.2K - $30.9K
3% of jobs
$30.9K - $37.6K
16% of jobs
$39.3K is the 25th percentile. Wages below this are outliers.
$37.6K - $44.3K
23% of jobs
The median wage is $46.3K / yr.
$44.3K - $51K
27% of jobs
$55.3K is the 75th percentile. Wages above this are outliers.
$51K - $57.7K
10% of jobs
$57.7K - $64.4K
4% of jobs
$64.4K - $71.1K
5% of jobs
$71.1K - $77.8K
2% of jobs
$77.8K - $84.5K
2% of jobs
$84.5K - $91.2K
2% of jobs
$91.2K - $97.9K
5% of jobs
$24.2K
$54.3K
$97.9K
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.
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.
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.
For Fda Inspector jobs in Dallas, TX, the most frequently searched job titles are:
The top searched job categories for Fda Inspector jobs in Dallas, TX are:
Cities near Dallas, TX with the most Fda Inspector job openings:

Contractor
Re-posted 14 days ago
7.0
Based on 5 frontline employees who took The Breakroom Quiz
PER DIEM OPPORTUNITIES AVAILABLE
Onsite Women's Health is on a mission to improve women's healthcare.
In partnership with forward-thinking providers across the country, Onsite Women's Health offers comprehensive mammography services with clinical expertise, innovative technology, and proprietary protocols that delivers personalized, convenient breast care for the patient.
The Opportunity
The OWH program is unparalleled, making breast cancer screening more convenient for women.
Do you want a flexible work schedule?
Can you be available to cover on a moment's notice?
Do you want to experience different office environments?
Then come to Onsite Women's Health as a Per Diem Technologist!
See yourself here.
At Onsite we don't work weekends or after hours and offer the opportunity to use the latest 3D tomosynthesis digital mammography equipment in an OB/Gyn office environment.
If you are an experienced mammographer, someone who can work independently and wants to have an impact on each and every patient, join us as a Per Diem.
What do you need to be the right candidate for this role?
What are your responsibilities?
Exceptional compensation for the right candidate!
Experience:
License:
EOE M/F/V/H
Get the full story on Breakroom
Sourced by ZipRecruiter
Health care and social assistance
201 - 500 Employees
Nashville, TN, US
2008