FDA Technical Consultant
Washington, DC ยท On-site
Office. Qualified candidates will have at least 5 years' experience as an FDA investigator or a senior role in global quality, to assist our FDA team in responding to FDA inspections at ...
Washington, DC ยท On-site
Office. Qualified candidates will have at least 5 years' experience as an FDA investigator or a senior role in global quality, to assist our FDA team in responding to FDA inspections at ...
Washington, DC ยท On-site
Office. Qualified candidates will have at least 5 years' experience as an FDA investigator or a senior role in global quality, to assist our FDA team in responding to FDA inspections at ...
Washington, DC ยท On-site +1
Office. Qualified candidates will have at least 5 years' experience as an FDA investigator or a senior role in global quality, to assist our FDA team in responding to FDA inspections at ...
Washington, DC ยท On-site +1
Office. Qualified candidates will have at least 5 years' experience as an FDA investigator or a senior role in global quality, to assist our FDA team in responding to FDA inspections at ...
Durham, NC ยท On-site
This individual will play a key role in maintaining compliance with FDA regulations and applicable accreditation standards by leading investigations, authoring quality documentation, and partnering ...
Durham, NC ยท On-site
This individual will play a key role in maintaining compliance with FDA regulations and applicable accreditation standards by leading investigations, authoring quality documentation, and partnering ...
Bothell, WA ยท On-site
Own and present CAPA effectiveness, investigation quality, risk assessments, and HHE processes during FDA interactions. * Act as the primary presenter/interface for FDA inspections, regulatory ...
Quick apply
Bothell, WA ยท On-site
Own and present CAPA effectiveness, investigation quality, risk assessments, and HHE processes during FDA interactions. * Act as the primary presenter/interface for FDA inspections, regulatory ...
Chicago, IL ยท On-site
$180 - $240/hr
Working knowledge of FDA regulations, ICH-GCP, and IRB processes. * Strong leadership ... Sub-Investigator track (no prior PI experience required) * MD, DO, NP, or PA with an active ...
Chicago, IL ยท On-site
$180 - $240/hr
Working knowledge of FDA regulations, ICH-GCP, and IRB processes. * Strong leadership ... Sub-Investigator track (no prior PI experience required) * MD, DO, NP, or PA with an active ...
Chicago, IL ยท On-site
$47K - $48K/yr
Working knowledge of FDA regulations, ICH-GCP, and IRB processes. * Strong leadership ... Sub-Investigator track (no prior PI experience required) * MD, DO, NP, or PA with an active ...
Chicago, IL ยท On-site
$47K - $48K/yr
Working knowledge of FDA regulations, ICH-GCP, and IRB processes. * Strong leadership ... Sub-Investigator track (no prior PI experience required) * MD, DO, NP, or PA with an active ...
Chicago, IL ยท On-site
$47K - $48K/yr
Working knowledge of FDA regulations, ICH-GCP, and IRB processes. * Strong leadership ... Sub-Investigator track (no prior PI experience required) * MD, DO, NP, or PA with an active ...
Chicago, IL ยท On-site
$47K - $48K/yr
Working knowledge of FDA regulations, ICH-GCP, and IRB processes. * Strong leadership ... Sub-Investigator track (no prior PI experience required) * MD, DO, NP, or PA with an active ...
Working knowledge of FDA regulations, ICH-GCP, and IRB processes. * Strong leadership ... Sub-Investigator track (no prior PI experience required) * MD, DO, NP, or PA with an active ...
Quick apply
Working knowledge of FDA regulations, ICH-GCP, and IRB processes. * Strong leadership ... Sub-Investigator track (no prior PI experience required) * MD, DO, NP, or PA with an active ...
Pine Brook, NJ ยท On-site +1
Compounding rules, regulations and FDA guidance o 503A o 503B o Bulk API suppliers and repackagers o FDA audits/investigations * Drug supply chain security and track and trace o Trading partner ...
Quick apply
Pine Brook, NJ ยท On-site +1
Compounding rules, regulations and FDA guidance o 503A o 503B o Bulk API suppliers and repackagers o FDA audits/investigations * Drug supply chain security and track and trace o Trading partner ...
Houma, LA ยท On-site
$45K - $45K/yr
The PI retains ultimate responsibility for the conduct of assigned studies in accordance with FDA ... Serve as Principal Investigator for industry-sponsored clinical trials within assigned therapeutic ...
Quick apply
Houma, LA ยท On-site
$45K - $45K/yr
The PI retains ultimate responsibility for the conduct of assigned studies in accordance with FDA ... Serve as Principal Investigator for industry-sponsored clinical trials within assigned therapeutic ...
Viera, FL ยท On-site
$43K - $43K/yr
The PI retains ultimate responsibility for the conduct of assigned studies in accordance with FDA ... Serve as Principal Investigator for industry-sponsored clinical trials within assigned therapeutic ...
Viera, FL ยท On-site
$43K - $43K/yr
The PI retains ultimate responsibility for the conduct of assigned studies in accordance with FDA ... Serve as Principal Investigator for industry-sponsored clinical trials within assigned therapeutic ...
Houma, LA ยท On-site
$45K - $45K/yr
The PI retains ultimate responsibility for the conduct of assigned studies in accordance with FDA ... Serve as Principal Investigator for industry-sponsored clinical trials within assigned therapeutic ...
Houma, LA ยท On-site
$45K - $45K/yr
The PI retains ultimate responsibility for the conduct of assigned studies in accordance with FDA ... Serve as Principal Investigator for industry-sponsored clinical trials within assigned therapeutic ...
Covington, LA ยท On-site
$40K - $40K/yr
The PI retains ultimate responsibility for the conduct of assigned studies in accordance with FDA ... Serve as Principal Investigator for industry-sponsored clinical trials within assigned therapeutic ...
Quick apply
Covington, LA ยท On-site
$40K - $40K/yr
The PI retains ultimate responsibility for the conduct of assigned studies in accordance with FDA ... Serve as Principal Investigator for industry-sponsored clinical trials within assigned therapeutic ...
Covington, LA ยท On-site
$40K - $40K/yr
The PI retains ultimate responsibility for the conduct of assigned studies in accordance with FDA ... Serve as Principal Investigator for industry-sponsored clinical trials within assigned therapeutic ...
Covington, LA ยท On-site
$40K - $40K/yr
The PI retains ultimate responsibility for the conduct of assigned studies in accordance with FDA ... Serve as Principal Investigator for industry-sponsored clinical trials within assigned therapeutic ...
FL ยท On-site
$43K - $43K/yr
The PI retains ultimate responsibility for the conduct of assigned studies in accordance with FDA ... Serve as Principal Investigator for industry-sponsored clinical trials within assigned therapeutic ...
FL ยท On-site
$43K - $43K/yr
The PI retains ultimate responsibility for the conduct of assigned studies in accordance with FDA ... Serve as Principal Investigator for industry-sponsored clinical trials within assigned therapeutic ...
Viera, FL ยท On-site
$43K - $43K/yr
The PI retains ultimate responsibility for the conduct of assigned studies in accordance with FDA ... Serve as Principal Investigator for industry-sponsored clinical trials within assigned therapeutic ...
Quick apply
Viera, FL ยท On-site
$43K - $43K/yr
The PI retains ultimate responsibility for the conduct of assigned studies in accordance with FDA ... Serve as Principal Investigator for industry-sponsored clinical trials within assigned therapeutic ...
Houma, LA ยท On-site
$45K - $45K/yr
The PI retains ultimate responsibility for the conduct of assigned studies in accordance with FDA ... Serve as Principal Investigator for industry-sponsored clinical trials within assigned therapeutic ...
Houma, LA ยท On-site
$45K - $45K/yr
The PI retains ultimate responsibility for the conduct of assigned studies in accordance with FDA ... Serve as Principal Investigator for industry-sponsored clinical trials within assigned therapeutic ...
Covington, LA ยท On-site
$40K - $40K/yr
The PI retains ultimate responsibility for the conduct of assigned studies in accordance with FDA ... Serve as Principal Investigator for industry-sponsored clinical trials within assigned therapeutic ...
Covington, LA ยท On-site
$40K - $40K/yr
The PI retains ultimate responsibility for the conduct of assigned studies in accordance with FDA ... Serve as Principal Investigator for industry-sponsored clinical trials within assigned therapeutic ...
Brea, CA ยท On-site
$80K - $90K/yr
... an FDA investigator with confidence, this role was built for you. What You'll Do As the Calibration and Maintenance Supervisor, you will own two mission-critical programs and lead the team that ...
Brea, CA ยท On-site
$80K - $90K/yr
... an FDA investigator with confidence, this role was built for you. What You'll Do As the Calibration and Maintenance Supervisor, you will own two mission-critical programs and lead the team that ...
Serve as Principal Investigator or Sub-Investigator on FDA form 1572 for protocols conducted. * Satisfactorily perform and comply with all responsibilities of a clinical investigator including, but ...
Serve as Principal Investigator or Sub-Investigator on FDA form 1572 for protocols conducted. * Satisfactorily perform and comply with all responsibilities of a clinical investigator including, but ...
$32K - $41K
7% of jobs
$41K - $50K
14% of jobs
$51.5K is the 25th percentile. Wages below this are outliers.
$50K - $59K
24% of jobs
The median wage is $63.5K / yr.
$59K - $68K
9% of jobs
$68K - $77K
5% of jobs
$77K - $86K
15% of jobs
$86.8K is the 75th percentile. Wages above this are outliers.
$86K - $95K
3% of jobs
$95K - $104K
6% of jobs
$104K - $113K
4% of jobs
$113K - $122K
12% of jobs
$122K - $131K
0% of jobs
$32K
$75.3K
$131K
An FDA Investigator is responsible for inspecting facilities that manufacture, process, or distribute regulated products, including food, drugs, medical devices, and cosmetics. They ensure compliance with federal regulations, identify violations, and document findings through reports. Investigators may also collect samples, review records, and participate in enforcement actions when necessary. Their work helps protect public health by ensuring the safety, efficacy, and quality of products entering the market.
A typical day for an FDA Investigator involves conducting on-site inspections of food, drug, medical device, or cosmetic manufacturers to ensure compliance with federal regulations. Investigators review production processes, collect samples, examine records, and interview facility staff to assess safety and quality standards. The role often includes significant report writing and follow-up activities to document findings and recommend corrective actions. While much of the work is independent, FDA Investigators also collaborate closely with colleagues, regulatory officials, and industry representatives to resolve issues and maintain public health standards.
To thrive as an FDA Investigator, you need a background in science or public health, strong analytical skills, and often a bachelor's degree in a related field. Familiarity with regulatory databases, laboratory sampling equipment, and federal inspection protocols is typically required. Effective communication, meticulous attention to detail, and strong organizational skills help investigators excel in documenting findings and interacting with diverse stakeholders. These attributes are crucial for ensuring compliance with federal regulations and protecting public health.
Cities with the most Fda Investigator job openings:
The most popular types of Fda Investigator jobs are:
States with the most job openings for Fda Investigator jobs include:
The top searched job categories for Fda Investigator jobs are:

Full-time
Re-posted 27 days ago