FDA Egg Safety Rule Inspections - Federal inspections consist of reviewing egg production facilities SE Prevention Plans, reviewing supporting records to assure compliance with the FDA Egg Rule ...
FDA Egg Safety Rule Inspections - Federal inspections consist of reviewing egg production facilities SE Prevention Plans, reviewing supporting records to assure compliance with the FDA Egg Rule ...
Quality Inspector
$20 - $23/hr
... ISO, FDA, and internal quality requirements · Collect, analyze, and document quality data to support continuous improvement efforts · Maintain accurate records of inspections, non-conformance ...
Quick apply
Quality Inspector
$20 - $23/hr
... ISO, FDA, and internal quality requirements · Collect, analyze, and document quality data to support continuous improvement efforts · Maintain accurate records of inspections, non-conformance ...
... FDA 21 CFR 820 requirements as well as company protocols. Job Responsibilities: * Adheres to ... Complete required documentation and inspection operations with detail, accuracy, and precision.
... FDA 21 CFR 820 requirements as well as company protocols. Job Responsibilities: * Adheres to ... Complete required documentation and inspection operations with detail, accuracy, and precision.
... FDA 21 CFR 820 requirements as well as company protocols. Job Responsibilities: * Adheres to ... Complete required documentation and inspection operations with detail, accuracy, and precision.
... FDA 21 CFR 820 requirements as well as company protocols. Job Responsibilities: * Adheres to ... Complete required documentation and inspection operations with detail, accuracy, and precision.
... FDA 21 CFR 820 requirements as well as company protocols. Job Responsibilities: * Adheres to ... Complete required documentation and inspection operations with detail, accuracy, and precision.
... FDA 21 CFR 820 requirements as well as company protocols. Job Responsibilities: * Adheres to ... Complete required documentation and inspection operations with detail, accuracy, and precision.
Quality Inspector
Fort Wayne, IN · On-site
... FDA 21 CFR 820 requirements as well as company protocols. Job Responsibilities: * Adheres to ... Complete required documentation and inspection operations with detail, accuracy, and precision.
Quality Inspector
Fort Wayne, IN · On-site
... FDA 21 CFR 820 requirements as well as company protocols. Job Responsibilities: * Adheres to ... Complete required documentation and inspection operations with detail, accuracy, and precision.
Be Seen First
Machinist / Inspector - Medical Device Manufacturing
Avon, IN · On-site
$40K - $55K/yr
Familiarity with ISO 13485, FDA-regulated manufacturing, or quality system documentation. * Experience with first article inspection, in-process inspection, final inspection, and nonconforming ...
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Be Seen First
Machinist / Inspector - Medical Device Manufacturing
Avon, IN · On-site
$40K - $55K/yr
Familiarity with ISO 13485, FDA-regulated manufacturing, or quality system documentation. * Experience with first article inspection, in-process inspection, final inspection, and nonconforming ...
... FDA QMSR, ISO 13485, cGMP, cGDP, and EU MDR. • Ability to maintain accurate documentation and records. • Skilled in identifying and evaluating critical-to-quality attributes during inspection.
... FDA QMSR, ISO 13485, cGMP, cGDP, and EU MDR. • Ability to maintain accurate documentation and records. • Skilled in identifying and evaluating critical-to-quality attributes during inspection.
Compliance Manager
Brownsburg, IN · On-site
Participates in Regulatory/FDA inspections and audits by providing information or expediting/ obtaining information required by the inspectors/auditors. * Develops and manages the site data integrity ...
Compliance Manager
Brownsburg, IN · On-site
Participates in Regulatory/FDA inspections and audits by providing information or expediting/ obtaining information required by the inspectors/auditors. * Develops and manages the site data integrity ...
Demonstrated knowledge of FDA regulations (21 CFR Parts 210, 211), EU GMP Annex 1, ICH guidelines ... Experience with visual inspection methods (manual and automated), AQL sampling plans, and defect ...
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Demonstrated knowledge of FDA regulations (21 CFR Parts 210, 211), EU GMP Annex 1, ICH guidelines ... Experience with visual inspection methods (manual and automated), AQL sampling plans, and defect ...
... with FDA, EMA, and other applicable regulatory requirements. The QA Senior Engineer serves as a ... inspection, labeling, and packaging activities. Essential Job Functions: • Provide quality ...
... with FDA, EMA, and other applicable regulatory requirements. The QA Senior Engineer serves as a ... inspection, labeling, and packaging activities. Essential Job Functions: • Provide quality ...
The QA Senior Engineer of Inspection, Labeling, and Packaging is responsible for the oversight and ... with FDA, EMA, and other applicable regulatory requirements. The QA Senior Engineer serves as a ...
The QA Senior Engineer of Inspection, Labeling, and Packaging is responsible for the oversight and ... with FDA, EMA, and other applicable regulatory requirements. The QA Senior Engineer serves as a ...
... with FDA, EMA, and other applicable regulatory requirements. The QA Senior Engineer serves as a ... inspection, labeling, and packaging activities. Essential Job Functions: • Provide quality ...
... with FDA, EMA, and other applicable regulatory requirements. The QA Senior Engineer serves as a ... inspection, labeling, and packaging activities. Essential Job Functions: • Provide quality ...
Inspection Team Lead
Fishers, IN · On-site
Aware of industry guidances and requirements applicable to visual inspection, including USP and and FDA Draft Guidance: Inspection of Injectable Products for Visible Particulates (2021). Minimum ...
Inspection Team Lead
Fishers, IN · On-site
Aware of industry guidances and requirements applicable to visual inspection, including USP and and FDA Draft Guidance: Inspection of Injectable Products for Visible Particulates (2021). Minimum ...
... and FDA 21 CFR 820 requirements as well as company protocols. Job Responsibilities: Adheres to ... Complete required documentation and inspection operations with detail, accuracy, and precision.
... and FDA 21 CFR 820 requirements as well as company protocols. Job Responsibilities: Adheres to ... Complete required documentation and inspection operations with detail, accuracy, and precision.
... and FDA 21 CFR 820 requirements as well as company protocols. Job Responsibilities: Adheres to ... Complete required documentation and inspection operations with detail, accuracy, and precision.
... and FDA 21 CFR 820 requirements as well as company protocols. Job Responsibilities: Adheres to ... Complete required documentation and inspection operations with detail, accuracy, and precision.
... and FDA 21 CFR 820 requirements as well as company protocols. Job Responsibilities: Adheres to ... Complete required documentation and inspection operations with detail, accuracy, and precision.
... and FDA 21 CFR 820 requirements as well as company protocols. Job Responsibilities: Adheres to ... Complete required documentation and inspection operations with detail, accuracy, and precision.
Maintain expert knowledge of FDA, EMA, and other global regulatory requirements for sterile product inspection. People Development & Team Leadership * Recruit, develop, and retain high-performing ...
Maintain expert knowledge of FDA, EMA, and other global regulatory requirements for sterile product inspection. People Development & Team Leadership * Recruit, develop, and retain high-performing ...
Manager of Inspection
Fishers, IN · On-site
Maintain expert knowledge of FDA, EMA, and other global regulatory requirements for sterile product inspection. People Development & Team Leadership * Recruit, develop, and retain high-performing ...
Manager of Inspection
Fishers, IN · On-site
Maintain expert knowledge of FDA, EMA, and other global regulatory requirements for sterile product inspection. People Development & Team Leadership * Recruit, develop, and retain high-performing ...
Manager of Inspection
Fishers, IN · On-site
Maintain expert knowledge of FDA, EMA, and other global regulatory requirements for sterile product inspection. People Development & Team Leadership * Recruit, develop, and retain high-performing ...
Manager of Inspection
Fishers, IN · On-site
Maintain expert knowledge of FDA, EMA, and other global regulatory requirements for sterile product inspection. People Development & Team Leadership * Recruit, develop, and retain high-performing ...
Fda Inspector information
See Indiana salary details
$23.3K - $29.8K
3% of jobs
$29.8K - $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 $44.6K / yr.
$42.6K - $49.1K
27% of jobs
$53.2K is the 75th percentile. Wages above this are outliers.
$49.1K - $55.5K
10% of jobs
$55.5K - $62K
4% of jobs
$62K - $68.4K
5% of jobs
$68.4K - $74.9K
2% of jobs
$74.9K - $81.3K
2% of jobs
$81.3K - $87.8K
2% of jobs
$87.8K - $94.2K
5% of jobs
$23.3K
$52.3K
$94.2K
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 popular job titles related to Fda Inspector jobs in Indiana?
For Fda Inspector jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Fda Inspector jobs in Indiana look for?
The top searched job categories for Fda Inspector jobs in Indiana are:
- Remote International Microbiology
- Fda Regulatory
- Regulatory Labeling Manager
- Quality Control Manager Navfac Facilities
- Biology Degree Cosmetic
- It Risk And Assurance Manager
- Senior Food Safety Quality Assurance Manager
- Quality Assurance Laboratory Manager
- Regulatory Quality Specialist
- Director Quality Control Furniture

Full-time
Posted 11 days ago
Purdue University rating
7.5
Based on 136 frontline employees who took The Breakroom Quiz
312th of 618 rated colleges and universities
Job description
City: Richmond
Job Description:
Job Summary
Under the guidance of the supervisor, the Eastern Area Inspector is responsible for conducting several regulatory inspection activities within 22-counties in eastern Indiana. As the inspector, you will be responsible for ensuring compliance with applicable federal and state laws and regulations governing the production, distribution, labeling, and sale of shell eggs while maintaining professional relationships with industry stakeholders and regulatory partners.
The assigned territory includes the following counties: Bartholomew, Blackford, Dearborn, Decatur, Delaware, Fayette, Franklin, Grant, Hancock, Henry, Jay, Jefferson, Jennings, Madison, Ohio, Randolph, Ripley, Rush, Shelby, Switzerland, Union, and Wayne.
What You'll Be Doing:
- State Egg inspections consist of verifying packaging is properly labeled, eggs meet quality standards, and that the product is being maintained in an environment that promotes a safe product to the consumer
- FDA Egg Safety Rule Inspections - Federal inspections consist of reviewing egg production facilities SE Prevention Plans, reviewing supporting records to assure compliance with the FDA Egg Rule, preparing and/or reviewing comprehensive reports for submission to FDA
- USDA COOL Audits - Performing Country of Origin Labeling (COOL) Inspections at retail locations throughout Indiana for UDSA. Activities include preparing a final report of findings, communicating findings with retail management, and transmitting the information to the appropriate regulatory agency
- USDA/AMS Shell Egg Surveillance Inspections - Conducting shell egg surveillance inspection of USDA registered egg production facilities and hatchery operations as designated by the USDA/AMS under the Egg Products Inspection Act. Evaluating shell eggs to verify quality and confirm appropriate environmental controls
- Performing additional duties and special projects as assigned
What We're Looking For:
- Bachelor's Degree
- 6 months of food retail industry or food production/processing
- In lieu of degree, an equivalent combination of education and experience may also be considered (Associate's degree + 2.5 years of experience; HS/GED + 4.5 years of experience)
- Ability to pass an Office of Personnel Management (OPM) background screening and obtain/maintain FDA credentials and commission
- Have or be able to obtain certifications or accreditation within the first year of employment
- Obtain accreditation from FDA to complete inspections under 21CFR 118 Egg Safey Rule
- Obtain Shell Egg Grader and Surveillance certification through the USDA/AMS Poultry Program, under the Egg Quality Inspection Act
- Obtain certification to conduct COOL audits per USDA/AMS (Agricultural Marketing Service) COOL program
- Basic computer operation, organizational, time management, and communication/conflict resolution skills are essential
- Ability to establish own work schedule and be self-motivated to complete a level of work expected of the position
- Ability to conduct an inspection in a professional manner and record and submit findings to the appropriate agency
- Ability to understand and interpret laws and regulations pertaining to the inspection being conducted
- Ability to deal with potential conflict
- Ability to pass an annual respiratory physical and fitness test
- A good understanding of the retail food industry, including the production and distribution of shell eggs
- Valid U.S. or Canadian drivers license
- Travel
What We'd Like You to Know:
- The position is a remote position with the official work station being your residence
- All equipment required for the position is provided
- A vehicle for work activities is supplied
- Learn more about Purdue's benefits summary
- Purdue will not sponsor employment authorization for this position
- A Background Check is required for employment in this position
- FLSA: Exempt (Not Eligible For Overtime)
- Retirement Eligibility: Defined Contributions Waiting Period
Career Stream
Professional 1
Pay Band S055
Link to Purdue University's compensation guidelines
Job Code #200003104
Link to Career Path Maker
Who We Are
Purdue is a community built on collaboration, with global perspectives, Boilermaker pride and endless opportunity to live, learn and grow. Join us and contribute to our culture.
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About Purdue University
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Industry
Colleges, universities, and professional schools
Company size
10,000+ Employees
Headquarters location
West Lafayette, IN, US
Year founded
1962