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 ...
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 ...
Equipment Maintenance Technician (Packaging & Inspection) Location: Columbus, Ohio Job Summary: We ... Ensure all maintenance activities comply with GMP, FDA, and site SOPs * Document maintenance work ...
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Equipment Maintenance Technician (Packaging & Inspection) Location: Columbus, Ohio Job Summary: We ... Ensure all maintenance activities comply with GMP, FDA, and site SOPs * Document maintenance work ...
Maintain vision inspection & serialization systems (cameras, sensors, printers, scanners) * Work with PLC-controlled equipment to resolve alarms and faults * Ensure compliance with GMP, FDA, and SOP ...
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Maintain vision inspection & serialization systems (cameras, sensors, printers, scanners) * Work with PLC-controlled equipment to resolve alarms and faults * Ensure compliance with GMP, FDA, and SOP ...
Equipment Maintenance Technician (Packaging & Inspection) Location: Columbus, Ohio Job Summary: We ... Ensure all maintenance activities comply with GMP, FDA, and site SOPs * Document maintenance work ...
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Equipment Maintenance Technician (Packaging & Inspection) Location: Columbus, Ohio Job Summary: We ... Ensure all maintenance activities comply with GMP, FDA, and site SOPs * Document maintenance work ...
This role supports audits, investigations, CAPAs, and regulatory inspections while serving as a subject matter expert on data integrity (paper and electronic based) and FDA 21 CFR Part 11 ...
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This role supports audits, investigations, CAPAs, and regulatory inspections while serving as a subject matter expert on data integrity (paper and electronic based) and FDA 21 CFR Part 11 ...
... Inspection and In-Process Controls, CAPA, and Training. * Familiarity with ISO 14971 risk management principles and FDA 510(k) / Class II submission processes is advantageous. * Demonstrated ...
... Inspection and In-Process Controls, CAPA, and Training. * Familiarity with ISO 14971 risk management principles and FDA 510(k) / Class II submission processes is advantageous. * Demonstrated ...
... Inspection and In-Process Controls, CAPA, and Training. * Familiarity with ISO 14971 risk management principles and FDA 510(k) / Class II submission processes is advantageous. * Demonstrated ...
... Inspection and In-Process Controls, CAPA, and Training. * Familiarity with ISO 14971 risk management principles and FDA 510(k) / Class II submission processes is advantageous. * Demonstrated ...
... vision inspection systems such as Cognex or Systech * Experience supporting preventive maintenance and breakdown response activities * Familiarity with GMP and FDA regulated manufacturing ...
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... vision inspection systems such as Cognex or Systech * Experience supporting preventive maintenance and breakdown response activities * Familiarity with GMP and FDA regulated manufacturing ...
... inspection systems including cameras, sensors, and scanners • Assist with PLC-controlled equipment fault recovery and system resets • Ensure compliance with GMP, FDA, and site SOP standards • ...
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... inspection systems including cameras, sensors, and scanners • Assist with PLC-controlled equipment fault recovery and system resets • Ensure compliance with GMP, FDA, and site SOP standards • ...
Maintain serialization and vision inspection systems * Ensure compliance with GMP, FDA, and site procedures * Document maintenance activities and repairs accurately * Work closely with Production ...
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Maintain serialization and vision inspection systems * Ensure compliance with GMP, FDA, and site procedures * Document maintenance activities and repairs accurately * Work closely with Production ...
... inspection systems, and case packers. * Strong knowledge of cGMP regulations, FDA requirements, and validation lifecycle practices. * Experience writing and executing validation documentation (IQ/OQ ...
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... inspection systems, and case packers. * Strong knowledge of cGMP regulations, FDA requirements, and validation lifecycle practices. * Experience writing and executing validation documentation (IQ/OQ ...
... inspection systems, and case packers. * Strong knowledge of cGMP regulations, FDA requirements, and validation lifecycle practices. * Experience writing and executing validation documentation (IQ/OQ ...
... inspection systems, and case packers. * Strong knowledge of cGMP regulations, FDA requirements, and validation lifecycle practices. * Experience writing and executing validation documentation (IQ/OQ ...
... inspection systems, and case packers. * Strong knowledge of cGMP regulations, FDA requirements, and validation lifecycle practices. * Experience writing and executing validation documentation (IQ/OQ ...
... inspection systems, and case packers. * Strong knowledge of cGMP regulations, FDA requirements, and validation lifecycle practices. * Experience writing and executing validation documentation (IQ/OQ ...
... inspection equipment * Preventive and corrective maintenance activities * Support for PLC-driven equipment, vision systems, and serialization systems * GMP/FDA regulated manufacturing environment ...
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... inspection equipment * Preventive and corrective maintenance activities * Support for PLC-driven equipment, vision systems, and serialization systems * GMP/FDA regulated manufacturing environment ...
You'll lead inspection activities, support investigations, and help drive continuous improvement ... Maintain compliance with FDA GMP regulations and company quality systems. * Perform other duties as ...
You'll lead inspection activities, support investigations, and help drive continuous improvement ... Maintain compliance with FDA GMP regulations and company quality systems. * Perform other duties as ...
OH Underage Purchaser - Logan
Logan, OH · On-site
$17.75/hr
... inspections are coordinated with an FDA-commissioned (adult) Inspector, either in law enforcement or with related experience and state employment Purchaser will not deceive the retailer in any way ...
OH Underage Purchaser - Logan
Logan, OH · On-site
$17.75/hr
... inspections are coordinated with an FDA-commissioned (adult) Inspector, either in law enforcement or with related experience and state employment Purchaser will not deceive the retailer in any way ...
Experience supporting inspections performed by FDA and/or foreign regulatory authorities. * In-depth expertise in deviation management, change control, CAPA, and root cause analysis. * Strong ...
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Experience supporting inspections performed by FDA and/or foreign regulatory authorities. * In-depth expertise in deviation management, change control, CAPA, and root cause analysis. * Strong ...
Experience supporting inspections performed by FDA and/or foreign regulatory authorities. * In-depth expertise in deviation management, change control, CAPA, and root cause analysis. * Strong ...
Experience supporting inspections performed by FDA and/or foreign regulatory authorities. * In-depth expertise in deviation management, change control, CAPA, and root cause analysis. * Strong ...
Experience supporting inspections performed by FDA and/or foreign regulatory authorities. * In-depth expertise in deviation management, change control, CAPA, and root cause analysis. * Strong ...
Experience supporting inspections performed by FDA and/or foreign regulatory authorities. * In-depth expertise in deviation management, change control, CAPA, and root cause analysis. * Strong ...
Fda Inspector information
See salary details
$24.5K - $31.3K
3% of jobs
$31.3K - $38K
16% of jobs
$39.7K is the 25th percentile. Wages below this are outliers.
$38K - $44.8K
23% of jobs
The median wage is $46.9K / yr.
$44.8K - $51.6K
27% of jobs
$55.9K is the 75th percentile. Wages above this are outliers.
$51.6K - $58.4K
10% of jobs
$58.4K - $65.1K
4% of jobs
$65.1K - $71.9K
5% of jobs
$71.9K - $78.7K
2% of jobs
$78.7K - $85.5K
2% of jobs
$85.5K - $92.2K
2% of jobs
$92.2K - $99K
5% of jobs
$24.5K
$54.9K
$99K
How much do fda inspector jobs pay per year?

Quality Assurance Inspector - First and Second Shift - kdc/one Columbus
New Albany, OH • On-site
Other
Posted 4 days ago
Job description
As a Quality Assurance Inspector, you'll be ensuring our products meet our high standards from appearance and weight to regulatory compliance. You'll lead inspection activities, support investigations, and help drive continuous improvement across the production floor!
Shifts:
Monday-Friday
First: 6:30am-3:00pm
Second: 2:30pm-11:00pm
What You'll Be Doing:
- Evaluate product defects and recommend solutions during inspections.
- Keep Quality Management informed of any significant issues or trends.
- Investigate failures and deviations to identify root causes and implement corrective/preventive actions.
- Collaborate with production teams to coordinate schedules and support new product launches.
- Ensure all staff receive proper training in operations, cGMPs, safety, and environmental practices.
- Verify ongoing quality checks for appearance, weight, torque, and other specifications.
- Audit production records and forms for accuracy and completeness.
- Assist with daily quality checks and support the team as needed.
- Maintain compliance with FDA GMP regulations and company quality systems.
- Perform other duties as assigned.
What You'll Need to Succeed:
- High school diploma or GED; college coursework preferred.
- At least 2 years of experience in a quality-related role, ideally in a manufacturing setting.
- Familiarity with SAP is a plus.
- Proficient with measuring and testing devices.
- Strong computer skills, especially Microsoft Office.
- Excellent problem-solving and analytical abilities.
- Solid understanding of FDA GMPs and OSHA safety standards.
- Self-motivated with a strong work ethic.
- Clear communication with strong interpersonal and organizational skills.
- Able to manage multiple tasks and prioritize effectively.
- Detail-oriented and proactive in identifying potential issues.
KDC-ONE is an equal opportunity employer and does not discriminate on the basis of race, religion, color, national origin, age, sex, gender, disability or any other characteristic protected by law. I understand that employment with KDC-ONE Company is at-will, meaning that I or KDC-ONE Company may terminate my employment at any time, or for any reason consistent with applicable state or federal law. I understand that KDC-One requires the successful completion of a drug and/or alcohol test as a condition of employment.