Quality Inspector
Noblesville, IN · On-site
ISO 13485 · Ensure adherence with the quality manual and FDA Guidelines. · Perform IQOQPQ's for equipment and processes. · Apply critical thinking and discernment when evaluating inspection ...
New
Noblesville, IN · On-site
ISO 13485 · Ensure adherence with the quality manual and FDA Guidelines. · Perform IQOQPQ's for equipment and processes. · Apply critical thinking and discernment when evaluating inspection ...
New
Noblesville, IN · On-site
ISO 13485 · Ensure adherence with the quality manual and FDA Guidelines. · Perform IQOQPQ's for equipment and processes. · Apply critical thinking and discernment when evaluating inspection ...
New
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 ...
Fort Wayne, IN · On-site
$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 ...
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Fort Wayne, IN · On-site
$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 ...
Jeffersonville, IN · On-site
Comprehensive knowledge of medical device regulations and quality systems (e.g., ISO 13485, FDA 21 CFR Part 820). * Proven ability to lead teams, drive quality initiatives, and mentor inspectors on ...
Jeffersonville, IN · On-site
Comprehensive knowledge of medical device regulations and quality systems (e.g., ISO 13485, FDA 21 CFR Part 820). * Proven ability to lead teams, drive quality initiatives, and mentor inspectors on ...
... 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.
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.
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.
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.
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.
Warsaw, IN · On-site
$52 - $70/hr
Job Purpose:- The Quality Control Inspector at PRECISION MEDICAL TECHNOLOGIES is responsible for ... and FDA regulations relevant to medical devices.- Proficient in using precision measurement ...
Warsaw, IN · On-site
$52 - $70/hr
Job Purpose:- The Quality Control Inspector at PRECISION MEDICAL TECHNOLOGIES is responsible for ... and FDA regulations relevant to medical devices.- Proficient in using precision measurement ...
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.
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.
Familiarity with ISO 13485, FDA-regulated manufacturing, or quality system documentation. * Experience with first article inspection, in-process inspection, final inspection, and nonconforming ...
Familiarity with ISO 13485, FDA-regulated manufacturing, or quality system documentation. * Experience with first article inspection, in-process inspection, final inspection, and nonconforming ...
Be Seen First
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
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 ...
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 ...
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 ...
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 ...
... 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 ...
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... 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 ...
... 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 ...
... 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.
S. Food and Drug Administration (FDA) regulations, company policies and procedures, and customer requirements. * Manage daily performance and attendance of Quality Personnel in the inspection ...
S. Food and Drug Administration (FDA) regulations, company policies and procedures, and customer requirements. * Manage daily performance and attendance of Quality Personnel in the inspection ...
Indianapolis, IN · On-site
S. Food and Drug Administration (FDA) regulations, company policies and procedures, and customer requirements. * Manage daily performance and attendance of Quality Personnel in the inspection ...
Indianapolis, IN · On-site
S. Food and Drug Administration (FDA) regulations, company policies and procedures, and customer requirements. * Manage daily performance and attendance of Quality Personnel in the inspection ...
$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
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.
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.
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.
For Fda Inspector jobs in Indiana, the most frequently searched job titles are:
The top searched job categories for Fda Inspector jobs in Indiana are:

Quality Inspector - 2nd Shift
Nexxt Spine LLC, Noblesville, IN
Nexxt Spine LLC, is a leader in the medical device industry, dedicated to designing, manufacturing, and distributing an expanding portfolio of innovative spinal implants and instruments. We are committed to a culture of innovation, excellence, and employee engagement while delivering solutions that improve patient outcomes and strengthen surgeon and distributor partnerships.
Position Summary: Reporting to the Quality Director, the Quality Inspector will utilize quality inspection tools and practices for the effective and efficient development, transfer and maintenance of products and processes throughout the product lifecycle. The position will also collaborate with cross-functional teams to contribute to the overall success of the organization.
Essential Job Functions:
· Receive and inspect implants, instruments and raw materials.
· Assist Quality Engineer in establishing, implementing, and maintaining the Quality Management System.
· Complete product inspections in accordance with FDA guidelines for cGMP amp; ISO 13485
· Ensure adherence with the quality manual and FDA Guidelines.
· Perform IQOQPQ's for equipment and processes.
· Apply critical thinking and discernment when evaluating inspection results, identifying potential defects, inconsistencies, or areas of concern, and determining when issues require additional investigation or escalation.
· Various other tasks relevant to a growing business.
Qualifications:
· Basic ability to read and understand blueprints or technical drawings.
· Basic experience using measuring tools such as calipers, micrometers, and gauges.
· The ability to communicate effectively across departments and management tiers is essential.
· Preferred candidate will possess both team collaboration experience and the capability to work autonomously.
· Demonstrated ability to evaluate information objectively, ask questions, identify inconsistencies, and exercise sound judgment; particularly when requirements or inspection results require further consideration.
Physical Requirements:
· Sitting and standing for extended periods of time.
· Ability to lift up to 25 pounds.
· Hand dexterity for working with spinal implants and instrumentation.
Sourced by ZipRecruiter
Medical equipment and supplies manufacturing
11 - 50 Employees
Noblesville, IN, US
2009