Regulatory Manager
Columbus, OH · On-site
Lead responses to FDA inspections, audits, and customer inquiries * Ensure labeling compliance and regulatory submissions (e.g., SPL, CARES Act reporting) * Oversee change control, deviations, CAPAs ...
Regulatory Manager
Columbus, OH · On-site
Lead responses to FDA inspections, audits, and customer inquiries * Ensure labeling compliance and regulatory submissions (e.g., SPL, CARES Act reporting) * Oversee change control, deviations, CAPAs ...
Lead responses to FDA inspections, audits, and customer inquiries * Ensure labeling compliance and regulatory submissions (e.g., SPL, CARES Act reporting) * Oversee change control, deviations, CAPAs ...
Lead responses to FDA inspections, audits, and customer inquiries * Ensure labeling compliance and regulatory submissions (e.g., SPL, CARES Act reporting) * Oversee change control, deviations, CAPAs ...
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 ...
Quality Supervisor
Obetz, OH · On-site
Support external audits (ISO certification bodies, FDA inspections, customer audits). Quality Management System (QMS) Oversight * Support and maintain the ISO 13485 Quality Management System.
Quality Supervisor
Obetz, OH · On-site
Support external audits (ISO certification bodies, FDA inspections, customer audits). Quality Management System (QMS) Oversight * Support and maintain the ISO 13485 Quality Management System.
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 ...
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Quality Supervisor
Obetz, OH · On-site
$69K - $85K/yr
Support external audits (ISO certification bodies, FDA inspections, customer audits). Quality Management System (QMS) Oversight * Support and maintain the ISO 13485 Quality Management System.
Quick apply
Be Seen First
Quality Supervisor
Obetz, OH · On-site
$69K - $85K/yr
Support external audits (ISO certification bodies, FDA inspections, customer audits). Quality Management System (QMS) Oversight * Support and maintain the ISO 13485 Quality Management System.
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 ...
Quick apply
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 ...
Quality Supervisor
Obetz, OH · On-site
Support external audits (ISO certification bodies, FDA inspections, customer audits). Quality Management System (QMS) Oversight * Support and maintain the ISO 13485 Quality Management System.
Quality Supervisor
Obetz, OH · On-site
Support external audits (ISO certification bodies, FDA inspections, customer audits). Quality Management System (QMS) Oversight * Support and maintain the ISO 13485 Quality Management System.
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 ...
Quick apply
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 ...
Quick apply
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 ...
... 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 ...
Quick apply
... 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 • ...
Quality Technician - 2nd Shift
Groveport, OH · On-site
$17 - $23/hr
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 ...
Quality Technician - 2nd Shift
Groveport, OH · On-site
$17 - $23/hr
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 ...
Quality Technician - 2nd Shift
Groveport, OH · On-site
$17 - $23/hr
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 ...
Quality Technician - 2nd Shift
Groveport, OH · On-site
$17 - $23/hr
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 ...
Maintain serialization and vision inspection systems * Ensure compliance with GMP, FDA, and site procedures * Document maintenance activities and repairs accurately * Work closely with Production ...
Quick apply
Maintain serialization and vision inspection systems * Ensure compliance with GMP, FDA, and site procedures * Document maintenance activities and repairs accurately * Work closely with Production ...
Quality Technician - 2nd Shift
Groveport, OH · On-site
$17 - $23/hr
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 ...
Quality Technician - 2nd Shift
Groveport, OH · On-site
$17 - $23/hr
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 ...
Quality Technician - 2nd Shift
Groveport, OH · On-site
$17 - $23/hr
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 ...
Quality Technician - 2nd Shift
Groveport, OH · On-site
$17 - $23/hr
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 ...
... inspection systems, and case packers. * Strong knowledge of cGMP regulations, FDA requirements, and validation lifecycle practices. * Experience writing and executing validation documentation (IQ/OQ ...
Quick apply
... 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 ...
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?
As of Jul 1, 2026, the average yearly pay for fda inspector in the United States is $54,939.00, according to ZipRecruiter salary data. Most workers in this role earn between $38,500.00 and $63,500.00 per year, depending on experience, location, and employer.
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Job description
At Safecor Health, our mission is simple but powerful: help hospitals deliver medications safely, efficiently, and reliably.
As the nation's largest independently owned medication repackaging company, we support over 1,000 hospitals and healthcare systems across the country. Behind every unit-dose product is a team driven by our core values:
Care Commitment Excellence
We're looking for a Manager, Quality Assurance & Regulatory to lead critical quality and regulatory initiatives that ensure our products meet the highest standards-and ultimately protect patient safety.
The Opportunity
This is a high-impact leadership role responsible for shaping and maintaining FDA-compliant Quality Systems, driving regulatory strategy, and ensuring operational excellence across our organization.
You'll partner across teams, influence key decisions, and play a vital role in keeping Safecor in a constant state of compliance and readiness.
What You'll Do
What You Bring
At Safecor, you're not just maintaining compliance-you're helping ensure that patients receive medications safely when they need them most.
You'll be part of a team that:
If you're passionate about quality, regulatory excellence, and making a real difference in healthcare-we'd love to hear from you.
As the nation's largest independently owned medication repackaging company, we support over 1,000 hospitals and healthcare systems across the country. Behind every unit-dose product is a team driven by our core values:
Care Commitment Excellence
We're looking for a Manager, Quality Assurance & Regulatory to lead critical quality and regulatory initiatives that ensure our products meet the highest standards-and ultimately protect patient safety.
The Opportunity
This is a high-impact leadership role responsible for shaping and maintaining FDA-compliant Quality Systems, driving regulatory strategy, and ensuring operational excellence across our organization.
You'll partner across teams, influence key decisions, and play a vital role in keeping Safecor in a constant state of compliance and readiness.
What You'll Do
- Lead and maintain FDA-compliant Quality Systems (21 CFR Parts 210, 211, 820, 11, and 4)
- Drive quality strategy, ensuring consistent production aligned with regulatory standards
- Oversee vendor qualification programs, including audits and evaluations
- Lead regulatory activities, including FDA/DEA interactions and field actions
- Manage and enhance stability programs, including coordination with external labs
- Provide quality oversight for contract packaging and outsourcing programs
- Lead responses to FDA inspections, audits, and customer inquiries
- Ensure labeling compliance and regulatory submissions (e.g., SPL, CARES Act reporting)
- Oversee change control, deviations, CAPAs, and batch record review/release
- Drive continuous improvement through regulatory intelligence and quality system enhancements
- Partner cross-functionally and across sites to strengthen quality processes
What You Bring
- Bachelor's degree in a scientific field (or equivalent experience)
- 5+ years in pharmaceutical or medical device industry, with regulatory experience
- Proven experience with FDA regulations and Quality Systems development
- Leadership experience managing people and/or complex processes
- Experience supporting or leading FDA inspections and audits
- Strong knowledge of ICH guidelines, DEA regulations (preferred), and cGMP environments
- Exceptional communication, organization, and problem-solving skills
- A proactive, solutions-oriented mindset with a drive for continuous improvement
At Safecor, you're not just maintaining compliance-you're helping ensure that patients receive medications safely when they need them most.
You'll be part of a team that:
- Cares deeply about patients and each other
- Is committed to doing the right thing
- Strives for excellence in everything we do
If you're passionate about quality, regulatory excellence, and making a real difference in healthcare-we'd love to hear from you.
About Safecor Health
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
51 - 200 Employees
Headquarters location
Columbus, OH, US
Year founded
2008