MHRA, EMA, FDA); * Manage training for Medpace stakeholders with respect to inspection readiness; * Conducting inspection readiness visits at selected sites (as applicable) to assess inspection risk;
MHRA, EMA, FDA); * Manage training for Medpace stakeholders with respect to inspection readiness; * Conducting inspection readiness visits at selected sites (as applicable) to assess inspection risk;
MHRA, EMA, FDA); * Manage training for Medpace stakeholders with respect to inspection readiness; * Conducting inspection readiness visits at selected sites (as applicable) to assess inspection risk;
MHRA, EMA, FDA); * Manage training for Medpace stakeholders with respect to inspection readiness; * Conducting inspection readiness visits at selected sites (as applicable) to assess inspection risk;
... 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 ...
Sanitation Supervisor
West Chester, OH · On-site
Develops and maintains standard operating procedures aligned with USDA/FDA standards. * Conducts regular inspections of facilities and production lines to ensure compliance with Sanitation ...
Sanitation Supervisor
West Chester, OH · On-site
Develops and maintains standard operating procedures aligned with USDA/FDA standards. * Conducts regular inspections of facilities and production lines to ensure compliance with Sanitation ...
Develops and maintains standard operating procedures aligned with USDA/FDA standards. * Conducts regular inspections of facilities and production lines to ensure compliance with Sanitation ...
Develops and maintains standard operating procedures aligned with USDA/FDA standards. * Conducts regular inspections of facilities and production lines to ensure compliance with Sanitation ...
Sanitation Supervisor
Fairfield, OH · On-site
Develops and maintains standard operating procedures aligned with USDA/FDA standards. * Conducts regular inspections of facilities and production lines to ensure compliance with Sanitation ...
Sanitation Supervisor
Fairfield, OH · On-site
Develops and maintains standard operating procedures aligned with USDA/FDA standards. * Conducts regular inspections of facilities and production lines to ensure compliance with Sanitation ...
Stability Administrator
Bedford, OH · On-site
$44K - $74K/yr
Compliance & Inspection Readiness * Ensure audit readiness for FDA and international inspections. * Support internal/external audits by providing accurate and complete documentation. * Ensure ...
Stability Administrator
Bedford, OH · On-site
$44K - $74K/yr
Compliance & Inspection Readiness * Ensure audit readiness for FDA and international inspections. * Support internal/external audits by providing accurate and complete documentation. * Ensure ...
Stability Administrator
Bedford, OH · On-site
$44K - $74K/yr
Compliance & Inspection Readiness * Ensure audit readiness for FDA and international inspections. * Support internal/external audits by providing accurate and complete documentation. * Ensure ...
Stability Administrator
Bedford, OH · On-site
$44K - $74K/yr
Compliance & Inspection Readiness * Ensure audit readiness for FDA and international inspections. * Support internal/external audits by providing accurate and complete documentation. * Ensure ...
Perform quality inspections on production lines to ensure compliance with FDA, cGMP, SOPs, and customer requirements. * Partner with Production and Quality Management to resolve quality issues in ...
Quick apply
Perform quality inspections on production lines to ensure compliance with FDA, cGMP, SOPs, and customer requirements. * Partner with Production and Quality Management to resolve quality issues in ...
Equipment Validation Supervisor
Bedford, OH · On-site
$59K - $120K/yr
Maintain inspection readiness for FDA, MHRA, and other global regulatory audits. * Review and approve validation protocols, reports, SOPs, and change controls. Project & Lifecycle Management * Lead ...
Equipment Validation Supervisor
Bedford, OH · On-site
$59K - $120K/yr
Maintain inspection readiness for FDA, MHRA, and other global regulatory audits. * Review and approve validation protocols, reports, SOPs, and change controls. Project & Lifecycle Management * Lead ...
Equipment Validation Supervisor
Bedford, OH · On-site
$59K - $120K/yr
Maintain inspection readiness for FDA, MHRA, and other global regulatory audits. * Review and approve validation protocols, reports, SOPs, and change controls. Project & Lifecycle Management * Lead ...
Equipment Validation Supervisor
Bedford, OH · On-site
$59K - $120K/yr
Maintain inspection readiness for FDA, MHRA, and other global regulatory audits. * Review and approve validation protocols, reports, SOPs, and change controls. Project & Lifecycle Management * Lead ...
Quality Engineer - Life Sciences
Cincinnati, OH · On-site
$69K - $89K/yr
This role partners cross-functionally to ensure compliance with ISO 9001, ISO 13485, FDA Quality ... Experience supporting in regulatory inspections, internal/external, and/or supplier audits.
Quick apply
Quality Engineer - Life Sciences
Cincinnati, OH · On-site
$69K - $89K/yr
This role partners cross-functionally to ensure compliance with ISO 9001, ISO 13485, FDA Quality ... Experience supporting in regulatory inspections, internal/external, and/or supplier audits.
... with FDA regulations and internal quality standards. The Sr. Engineer will serve as the site ... Support regulatory audits and inspections by providing accurate and complete validation ...
New
... with FDA regulations and internal quality standards. The Sr. Engineer will serve as the site ... Support regulatory audits and inspections by providing accurate and complete validation ...
New
Ensure automated inspection systems remain in a validated and inspection-ready state in accordance with FDA and global regulatory expectations. * Author and/or approve URS, FAT/SAT protocols ...
Ensure automated inspection systems remain in a validated and inspection-ready state in accordance with FDA and global regulatory expectations. * Author and/or approve URS, FAT/SAT protocols ...
Ensure automated inspection systems remain in a validated and inspection-ready state in accordance with FDA and global regulatory expectations. * Author and/or approve URS, FAT/SAT protocols ...
Ensure automated inspection systems remain in a validated and inspection-ready state in accordance with FDA and global regulatory expectations. * Author and/or approve URS, FAT/SAT protocols ...
Senior Quality Assurance Manager - BioScience
$117K - $175K/yr
Regulatory Compliance & Inspection ReadinessMaintain the facility in a constant state of readiness for FDA, EU, and other regulatory inspections.Actively participate in internal audits, customer ...
Senior Quality Assurance Manager - BioScience
$117K - $175K/yr
Regulatory Compliance & Inspection ReadinessMaintain the facility in a constant state of readiness for FDA, EU, and other regulatory inspections.Actively participate in internal audits, customer ...
Ensure automated inspection systems remain in a validated and inspection-ready state in accordance with FDA and global regulatory expectations. * Author and/or approve URS, FAT/SAT protocols ...
Ensure automated inspection systems remain in a validated and inspection-ready state in accordance with FDA and global regulatory expectations. * Author and/or approve URS, FAT/SAT protocols ...
Regulatory Compliance & Inspection Readiness * Maintain the facility in a constant state of readiness for FDA, EU, and other regulatory inspections. * Actively participate in internal audits ...
Regulatory Compliance & Inspection Readiness * Maintain the facility in a constant state of readiness for FDA, EU, and other regulatory inspections. * Actively participate in internal audits ...
Regulatory Compliance & Inspection Readiness * Maintain the facility in a constant state of readiness for FDA, EU, and other regulatory inspections. * Actively participate in internal audits ...
Regulatory Compliance & Inspection Readiness * Maintain the facility in a constant state of readiness for FDA, EU, and other regulatory inspections. * Actively participate in internal audits ...
Fda Inspector information
See Ohio salary details
$23.3K - $29.7K
3% of jobs
$29.7K - $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 $44.5K / yr.
$42.6K - $49K
27% of jobs
$53.2K is the 75th percentile. Wages above this are outliers.
$49K - $55.5K
10% of jobs
$55.5K - $61.9K
4% of jobs
$61.9K - $68.4K
5% of jobs
$68.4K - $74.8K
2% of jobs
$74.8K - $81.2K
2% of jobs
$81.2K - $87.7K
2% of jobs
$87.7K - $94.1K
5% of jobs
$23.3K
$52.2K
$94.1K
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 the most commonly searched types of Fda Inspector jobs in Ohio?
The most popular types of Fda Inspector jobs in Ohio are:
What are popular job titles related to Fda Inspector jobs in Ohio?
For Fda Inspector jobs in Ohio, the most frequently searched job titles are:
What job categories do people searching Fda Inspector jobs in Ohio look for?
The top searched job categories for Fda Inspector jobs in Ohio are:
What cities in Ohio are hiring for Fda Inspector jobs?
Cities in Ohio with the most Fda Inspector job openings:

Other
Medical, Retirement, PTO
Re-posted 15 days ago
Medpace rating
8.6
Based on 12 frontline employees who took The Breakroom Quiz
13th of 73 rated research
Job description
The successful candidate will be responsible for facilitating the management of sponsor audits, broad range of regulatory inspections (FDA, EMA, MHRA) and facilitating QA relationship with external clients. The position will also include conducting inspection readiness activities for Medpace and Medpace stakeholders.
Responsibilities
- Facilitating Medpace sponsor audits onsite;
- Review and assess responses to sponsor audit reports;
- Provide clarity to the Quality Management System (QMS) during sponsor audits and other external audits;
- Provide guidance to Medpace study teams during sponsor audits;
- Manage pre-inspection activities for Medpace inspections;
- Provide inspection data trends to the Quality Metrics group for executive management review;
- Manage the inspection backroom during regulatory inspections to facilitate the timely delivery of requested documents;
- Conduct mock interviews for subject matter experts (SMEs) during inspection preparation;
- Reviewing, and analyzing regulatory inspection data issued by regulatory authorities (e.g. MHRA, EMA, FDA);
- Manage training for Medpace stakeholders with respect to inspection readiness;
- Conducting inspection readiness visits at selected sites (as applicable) to assess inspection risk;
- Act as QA lead for inspections at Medpace;
- Provide as needed support for inspections at Medpace external clients (sponsors and investigator sites); and
- Maintain the memorializing of frequently asked questions repository for regulatory inspection.
Qualifications
- Bachelor's degree in science or a related field;
- Experience in conducting and supporting regulatory inspections is a plus (FDA, MHRA and EMA);
- Strong communication skills;
- Strong quality mindset;
- Experience in supporting or conducting audits;
- Excellent written and verbal communications skills in English;
- Independent thinking and planning ability;
- Experience with a wide range of computerized systems;
- Good time management skills;
- Ability to switch between both big picture view and attention to detail; and
- The ability to work well on a team as well as independently.
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace?
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
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- Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence
Collaborative Culture
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- Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
- Leadership throughout Medpace is both accessible and approachable
Continuous Growth & Development
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- Office based environment with on-site mentors
- Defined career paths with clear advancement opportunities
- Industry renowned onboarding and training programs designed to accelerate professional development
- Ongoing training and continuous learning opportunities throughout your career
- An environment that encourages employees to influence change, contribute ideas, and grow quickly
Other Employee Benefits
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- Competitive compensation programs that recognize and reward performance
- Comprehensive health, wellness, retirement, and PTO benefits
- Office based culture with occasional WFH that provides flexibility for eligible positions after training
- Company-sponsored social events and intramural sports
Cincinnati Headquarters Experience
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- A modern corporate campus designed to support collaboration and productivity
- Multiple on-site dining options in the heart of Madison Square
- Free on-site parking
- Convenient access to on-site 24-7 fitness and wellness facilities
What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
About Medpace
Sourced by ZipRecruiter
Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.
Industry
Medical equipment and supplies manufacturing
Company size
1,001 - 5,000 Employees
Headquarters location
Cincinnati, OH, US
Year founded
1992