Review and follow-up on inspection reports from government agencies such as Health Dept., Consumer Affairs, USDA, FDA, etc. * Completing applications for renewal of various licenses and permits.
Review and follow-up on inspection reports from government agencies such as Health Dept., Consumer Affairs, USDA, FDA, etc. * Completing applications for renewal of various licenses and permits.
Director, Regulatory & Administrative Affairs - Institute for Transformative Clinical Trials
Manhattan, NY · On-site
$165K - $217K/yr
Experience with FDA inspections and sponsor audits About Us Strength through Unity and Inclusion The Mount Sinai Health System is committed to fostering an environment where everyone can contribute ...
Director, Regulatory & Administrative Affairs - Institute for Transformative Clinical Trials
Manhattan, NY · On-site
$165K - $217K/yr
Experience with FDA inspections and sponsor audits About Us Strength through Unity and Inclusion The Mount Sinai Health System is committed to fostering an environment where everyone can contribute ...
... 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 ...
Experience supporting FDA audits and inspections * Familiarity with Kneat, ValGenesis, or other validation management tools * Strong troubleshooting and analytical skills
Quick apply
Experience supporting FDA audits and inspections * Familiarity with Kneat, ValGenesis, or other validation management tools * Strong troubleshooting and analytical skills
Director, Clinical Quality and Pharmacovigilance
Manhattan, NY · On-site
$200 - $215/hr
FDA, EMA, MHRA etc.), including sponsor pre-approval and pre-license inspections supporting marketing applications (NDA/MAA). * Prepare and support internal teams, sponsors, and/or clinical sites ...
Director, Clinical Quality and Pharmacovigilance
Manhattan, NY · On-site
$200 - $215/hr
FDA, EMA, MHRA etc.), including sponsor pre-approval and pre-license inspections supporting marketing applications (NDA/MAA). * Prepare and support internal teams, sponsors, and/or clinical sites ...
Director, Clinical Quality and Pharmacovigilance
$87K - $119K/yr
FDA, EMA, MHRA etc.), including sponsor pre-approval and pre-license inspections supporting marketing applications (NDA/MAA). * Prepare and support internal teams, sponsors, and/or clinical sites ...
Director, Clinical Quality and Pharmacovigilance
$87K - $119K/yr
FDA, EMA, MHRA etc.), including sponsor pre-approval and pre-license inspections supporting marketing applications (NDA/MAA). * Prepare and support internal teams, sponsors, and/or clinical sites ...
Director, Clinical Quality and Pharmacovigilance
New York, NY · On-site
$87K - $119K/yr
FDA, EMA, MHRA etc.), including sponsor pre-approval and pre-license inspections supporting marketing applications (NDA/MAA). * Prepare and support internal teams, sponsors, and/or clinical sites ...
Director, Clinical Quality and Pharmacovigilance
New York, NY · On-site
$87K - $119K/yr
FDA, EMA, MHRA etc.), including sponsor pre-approval and pre-license inspections supporting marketing applications (NDA/MAA). * Prepare and support internal teams, sponsors, and/or clinical sites ...
Director, Clinical Quality and Pharmacovigilance
New York, NY · Remote
$81K - $111K/yr
FDA, EMA, MHRA etc.), including sponsor pre-approval and pre-license inspections supporting marketing applications (NDA/MAA). * Prepare and support internal teams, sponsors, and/or clinical sites ...
Quick apply
Director, Clinical Quality and Pharmacovigilance
New York, NY · Remote
$81K - $111K/yr
FDA, EMA, MHRA etc.), including sponsor pre-approval and pre-license inspections supporting marketing applications (NDA/MAA). * Prepare and support internal teams, sponsors, and/or clinical sites ...
The ideal candidate will have strong experience with FDA regulations, regulatory submissions, and ... Support regulatory inspections, audits, and agency interactions * Monitor evolving regulatory ...
Quick apply
The ideal candidate will have strong experience with FDA regulations, regulatory submissions, and ... Support regulatory inspections, audits, and agency interactions * Monitor evolving regulatory ...
Ensure compliance with ISO 14971, ISO 13485, 21 CFR Part 820, ICH Q9 , and applicable FDA/EU ... Serve as the primary SME during regulatory inspections and client/customer audits. * Develop ...
Quick apply
Ensure compliance with ISO 14971, ISO 13485, 21 CFR Part 820, ICH Q9 , and applicable FDA/EU ... Serve as the primary SME during regulatory inspections and client/customer audits. * Develop ...
Quality Auditor - Edison
Edison, NJ · On-site
$18/hr
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
Quality Auditor - Edison
Edison, NJ · On-site
$18/hr
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 ...
Automation Engineer
Manhattan, NY · On-site
$130 - $150/hr
FDA-regulated/cGMP environment; strong communication/leadership/project management. * Preferred: Pharmaceutical/cGMP; serialization & vision inspection; BMS; utility systems (Purified Water, HVAC, ...
Automation Engineer
Manhattan, NY · On-site
$130 - $150/hr
FDA-regulated/cGMP environment; strong communication/leadership/project management. * Preferred: Pharmaceutical/cGMP; serialization & vision inspection; BMS; utility systems (Purified Water, HVAC, ...
Manager, Regulatory Publishing
White Plains, NY · On-site
$80K - $110K/yr
... FDA, EMA, ICH, etc). Job Duties • Manages staff who electronically format, publish electronic ... inspection activities • Provide Document authoring template training. • Maintains Authoring ...
Manager, Regulatory Publishing
White Plains, NY · On-site
$80K - $110K/yr
... FDA, EMA, ICH, etc). Job Duties • Manages staff who electronically format, publish electronic ... inspection activities • Provide Document authoring template training. • Maintains Authoring ...
Sanitation Supervisor
Manhattan, NY · Remote
... FDA, USDA, OSHA, GMP, and HACCP standards - Support third-party audits and regulatory inspections - Report and escalate food safety deviations or non-conformances immediately - Participate in root ...
Quick apply
Sanitation Supervisor
Manhattan, NY · Remote
... FDA, USDA, OSHA, GMP, and HACCP standards - Support third-party audits and regulatory inspections - Report and escalate food safety deviations or non-conformances immediately - Participate in root ...
Quality Auditor - Edison
Edison, NJ · On-site
$65 - $90/hr
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 ...
Quality Auditor - Edison
Edison, NJ · On-site
$65 - $90/hr
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 ...
Review and follow-up on inspection reports from government agencies such as Health Dept., Consumer Affairs, USDA, FDA, etc. * Completing applications for renewal of various licenses and permits.
Review and follow-up on inspection reports from government agencies such as Health Dept., Consumer Affairs, USDA, FDA, etc. * Completing applications for renewal of various licenses and permits.
Quality Engineer
Newark, NJ · On-site
$75K - $97K/yr
Understanding of cGMP regulations, FDA requirements, data integrity principles, and inspection readiness activities. * Experience supporting regulatory, customer, or third-party audits is preferred.
Quick apply
Quality Engineer
Newark, NJ · On-site
$75K - $97K/yr
Understanding of cGMP regulations, FDA requirements, data integrity principles, and inspection readiness activities. * Experience supporting regulatory, customer, or third-party audits is preferred.
Senior Quality Engineer
Manhattan, NY · On-site
$100 - $150/hr
Be involved in the medical device software design controls activities, in accordance with the FDA ... external inspections and regulatory and customer audits.* Provide CSV guidance, coaching ...
Senior Quality Engineer
Manhattan, NY · On-site
$100 - $150/hr
Be involved in the medical device software design controls activities, in accordance with the FDA ... external inspections and regulatory and customer audits.* Provide CSV guidance, coaching ...
... inspections, audits, and information requests. * Support change control assessments and evaluate ... Working knowledge of FDA regulations, guidance documents, and regulatory submission processes.
Quick apply
... inspections, audits, and information requests. * Support change control assessments and evaluate ... Working knowledge of FDA regulations, guidance documents, and regulatory submission processes.
Fda Inspector information
See Queens, NY salary details
$25.6K - $32.6K
3% of jobs
$32.6K - $39.7K
16% of jobs
$41.5K is the 25th percentile. Wages below this are outliers.
$39.7K - $46.8K
23% of jobs
The median wage is $48.9K / yr.
$46.8K - $53.8K
27% of jobs
$58.3K is the 75th percentile. Wages above this are outliers.
$53.8K - $60.9K
10% of jobs
$60.9K - $68K
4% of jobs
$68K - $75K
5% of jobs
$75K - $82.1K
2% of jobs
$82.1K - $89.2K
2% of jobs
$89.2K - $96.2K
2% of jobs
$96.2K - $103.3K
5% of jobs
$25.6K
$57.3K
$103.3K
How much do fda inspector jobs pay per year?
As of Sep 6, 2026, the average yearly pay for fda inspector in Queens, NY is $57,327.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,200.00 and $66,300.00 per year, depending on experience, location, and employer.
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?
To become an FDA inspector, candidates typically need a bachelor's degree in a relevant field such as biology, chemistry, or food science, along with experience in food safety, pharmaceuticals, or related areas. They must pass a written exam and a background check, and often undergo specialized training at the FDA's training center. Certification or licensing is not required but can enhance prospects in the field.
What are popular job titles related to Fda Inspector jobs in Queens, NY?
For Fda Inspector jobs in Queens, NY, the most frequently searched job titles are:
What job categories do people searching Fda Inspector jobs in Queens, NY look for?
The top searched job categories for Fda Inspector jobs in Queens, NY are:
What cities near Queens, NY are hiring for Fda Inspector jobs?
Cities near Queens, NY with the most Fda Inspector job openings:
Full-time
Medical, Dental, Vision, PTO
Re-posted 24 days ago
H Mart rating
6.4
Based on 21 frontline employees who took The Breakroom Quiz
Job description
Inspection and Compliance Specialist/ SM Administrator_ Bilingual(Koran, English)
Responsibilities, but not limited to:
- Develop and design the company's health and safety policies.
- Visit each store and identify hazardous workplace conditions and conduct internal inspection.
- Train employees on safety policies and procedures, and regulations pertaining to employee safety.
- Partner with various vendors to provide health and safety related services and manage the contract.
- Ensure compliance with all applicable federal and state health and safety regulations and ensures necessary records are maintained and prepared according to established guidelines.
- Assist in Occupational Safety and Health Administration (OSHA) inspections, providing inspectors with appropriate documents and identifying safety measures.
- Review and follow-up on inspection reports from government agencies such as Health Dept., Consumer Affairs, USDA, FDA, etc.
- Completing applications for renewal of various licenses and permits.
- Managing the facilities which are related to health and compliance issues.
Requirements:
- Bachelor's Degree required
- Excellent interpersonal skills required as well as ability to communicate effectively both verbally and in writing.
- Domestic Travel required
- Experience preferred, but not required
Work Hours & Benefits:
- MON-FRI, 9:00am to 6:00pm
- Company provided Lunch
- Health Insurance Coverage
- Dental and Vision Coverage
- PSL / PTO
- Paid Holidays per company policy
- Celebration & Condolence Benefits per company policy
- Eligibility to use Company owned Resort per company policy
- 5% Employee Points program with H Mart Smart Card
About Hmart
Sourced by ZipRecruiter
Industry
Retail and transportation and warehousing
Company size
51 - 200 Employees
Headquarters location
Lyndhurst, NJ, US