Regulatory Affairs Specialist (FDA, DEA )
$60K - $76K/yr
Support internal audits, site inspections, and responses to 483s or warning letters * Coordinate ... FULL_TIME
$60K - $76K/yr
Support internal audits, site inspections, and responses to 483s or warning letters * Coordinate ... FULL_TIME
$60K - $76K/yr
Support internal audits, site inspections, and responses to 483s or warning letters * Coordinate ... FULL_TIME
CoreFactor is searching for a Senior Validation Engineer on a permanent/full-time basis for a ... Maintain the FDA Inspection Package - master document index, CAPA records, pre-inspection checklist
CoreFactor is searching for a Senior Validation Engineer on a permanent/full-time basis for a ... Maintain the FDA Inspection Package - master document index, CAPA records, pre-inspection checklist
Redmond, WA · On-site
$120K - $160K/yr
This position is full-time onsite in Redmond, WA and will transition to our new Bothell, WA ... Lead FDA inspection readiness and audits for bioanalytical laboratories, including preparation ...
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Redmond, WA · On-site
$120K - $160K/yr
This position is full-time onsite in Redmond, WA and will transition to our new Bothell, WA ... Lead FDA inspection readiness and audits for bioanalytical laboratories, including preparation ...
Apply Early
Redmond, WA · On-site
$120K - $160K/yr
This position is full-time onsite in Redmond, WA and will transition to our new Bothell, WA ... Lead FDA inspection readiness and audits for bioanalytical laboratories, including preparation ...
Redmond, WA · On-site
$120K - $160K/yr
This position is full-time onsite in Redmond, WA and will transition to our new Bothell, WA ... Lead FDA inspection readiness and audits for bioanalytical laboratories, including preparation ...
$180K - $220K/yr
Sr. Director of Quality Compliance Full-Time | Senior Leadership Location: Greenville, SC (Onsite ... Lead inspection readiness programs and provide on-site support during regulatory inspections
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$180K - $220K/yr
Sr. Director of Quality Compliance Full-Time | Senior Leadership Location: Greenville, SC (Onsite ... Lead inspection readiness programs and provide on-site support during regulatory inspections
Apply Early
$180K - $220K/yr
Sr. Director of Quality Compliance Full-Time | Senior Leadership Location: Greenville, SC (Onsite ... Lead inspection readiness programs and provide on-site support during regulatory inspections
$180K - $220K/yr
Sr. Director of Quality Compliance Full-Time | Senior Leadership Location: Greenville, SC (Onsite ... Lead inspection readiness programs and provide on-site support during regulatory inspections
$18 - $21/hr
Quality Technician Food Manufacturing | Entry-Level | Full-Time Department | Quality Assurance ... Support internal SQF audits and FDA/USDA inspection readiness by organizing records and ensuring ...
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$18 - $21/hr
Quality Technician Food Manufacturing | Entry-Level | Full-Time Department | Quality Assurance ... Support internal SQF audits and FDA/USDA inspection readiness by organizing records and ensuring ...
Apply Early
Bridgeton, NJ · On-site
$18 - $21/hr
Quality Technician Food Manufacturing | Entry-Level | Full-Time Department | Quality Assurance ... Support internal SQF audits and FDA/USDA inspection readiness by organizing records and ensuring ...
Quick apply
Bridgeton, NJ · On-site
$18 - $21/hr
Quality Technician Food Manufacturing | Entry-Level | Full-Time Department | Quality Assurance ... Support internal SQF audits and FDA/USDA inspection readiness by organizing records and ensuring ...
Bridgeton, NJ · On-site
$18 - $21/hr
Quality Technician Food Manufacturing | Entry-Level | Full-Time Department | Quality Assurance ... Support internal SQF audits and FDA/USDA inspection readiness by organizing records and ensuring ...
Quick apply
Bridgeton, NJ · On-site
$18 - $21/hr
Quality Technician Food Manufacturing | Entry-Level | Full-Time Department | Quality Assurance ... Support internal SQF audits and FDA/USDA inspection readiness by organizing records and ensuring ...
Hawthorne, CA · On-site
$23 - $34/hr
Full-time Manufacturing Quality Inspector About Us Our company is a leading manufacturer of ... Verify product conformance to ISO 13485 and FDA regulations * Document inspection results, maintain ...
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Hawthorne, CA · On-site
$23 - $34/hr
Full-time Manufacturing Quality Inspector About Us Our company is a leading manufacturer of ... Verify product conformance to ISO 13485 and FDA regulations * Document inspection results, maintain ...
Apply Early
Saint Petersburg, FL · On-site
$18 - $21/hr
Job Type: Full-time Business Hours: 8:00AM- $;30PM, Monday-Friday Career Level: 1-3 Years ... Knowledge of GMP (good manufacturing processes) documentation and FDA preferred. * Strong computer ...
Saint Petersburg, FL · On-site
$18 - $21/hr
Job Type: Full-time Business Hours: 8:00AM- $;30PM, Monday-Friday Career Level: 1-3 Years ... Knowledge of GMP (good manufacturing processes) documentation and FDA preferred. * Strong computer ...
Saint Petersburg, FL · On-site
Petersburg, FL 33709 Job Type: Full-time, Regular Business Hours: 8:00 AM - 4:30 PM, Monday ... Knowledge of GMP documentation and FDA preferred. * Strong computer and analytical skills OTHER ...
Saint Petersburg, FL · On-site
Petersburg, FL 33709 Job Type: Full-time, Regular Business Hours: 8:00 AM - 4:30 PM, Monday ... Knowledge of GMP documentation and FDA preferred. * Strong computer and analytical skills OTHER ...
Shelton, CT · On-site
Job Type Full-time Description POSITION SUMMARY: The Quality Inspector will provide quality control ... Understanding of medical device industry standards- ISO 13485 and FDA GMP. * Ability to meet ...
Shelton, CT · On-site
Job Type Full-time Description POSITION SUMMARY: The Quality Inspector will provide quality control ... Understanding of medical device industry standards- ISO 13485 and FDA GMP. * Ability to meet ...
Petersburg, FL 33709 Job Type: Full-time, Regular Business Hours: 8:00 AM - 4:30 PM, Monday ... Knowledge of GMP documentation and FDA preferred. * Strong computer and analytical skills OTHER ...
Petersburg, FL 33709 Job Type: Full-time, Regular Business Hours: 8:00 AM - 4:30 PM, Monday ... Knowledge of GMP documentation and FDA preferred. * Strong computer and analytical skills OTHER ...
Baltimore, MD · Remote
$80K - $100K/yr
S.-Based) - Any Location Employment Type: Full-Time Position Summary We are seeking an experienced ... Serve as a regulatory subject matter expert during sponsor audits, FDA inspections, and ...
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Baltimore, MD · Remote
$80K - $100K/yr
S.-Based) - Any Location Employment Type: Full-Time Position Summary We are seeking an experienced ... Serve as a regulatory subject matter expert during sponsor audits, FDA inspections, and ...
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$21 - $35/hr
** **We are looking for full-time, career driven Mechanical Inspector. This position entails measuring ... FDA Regulations * USDA Regulations * Pharmaceuticals * Standard Operating Procedures (SOPs)
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$21 - $35/hr
** **We are looking for full-time, career driven Mechanical Inspector. This position entails measuring ... FDA Regulations * USDA Regulations * Pharmaceuticals * Standard Operating Procedures (SOPs)
Apply Early
Raynham, MA · On-site
$23 - $26/hr
The Quality Inspector will join our quality team in Raynham, MA on a full time basis. The ... Experience in FDA and ISO regulated environments * Familiarity with Document Release and Change ...
Raynham, MA · On-site
$23 - $26/hr
The Quality Inspector will join our quality team in Raynham, MA on a full time basis. The ... Experience in FDA and ISO regulated environments * Familiarity with Document Release and Change ...
Job Type Full-time Description **US Based Candidates Only** Granules Pharmaceuticals, Inc., located ... Lead as the site Quality representative during FDA inspections. * Lead the site in inspections ...
Job Type Full-time Description **US Based Candidates Only** Granules Pharmaceuticals, Inc., located ... Lead as the site Quality representative during FDA inspections. * Lead the site in inspections ...
Moorestown, NJ · On-site
$20 - $21/hr
Job Type Full-time Description Since 1946, The Jet Pulverizer Company, Inc. has been committed to ... external audits, including FDA inspections. * Ensure compliance with cGMP (current Good ...
Moorestown, NJ · On-site
$20 - $21/hr
Job Type Full-time Description Since 1946, The Jet Pulverizer Company, Inc. has been committed to ... external audits, including FDA inspections. * Ensure compliance with cGMP (current Good ...
Fremont, IN · On-site
$22.81/hr
... and FDA inspections. * Maintain allergen control documentation and ensure program compliance ... IND2 Employment Type: FULL_TIME
Fremont, IN · On-site
$22.81/hr
... and FDA inspections. * Maintain allergen control documentation and ensure program compliance ... IND2 Employment Type: FULL_TIME
$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
| Aspect | Full Time Fda Inspector | Part Time Fda Inspector |
|---|---|---|
| Credentials | Typically requires a bachelor's degree in life sciences or related field, plus FDA inspector certification | Same as full-time, but may have more flexible certification requirements |
| Work Environment | Full-time, on-site inspections at manufacturing facilities, laboratories, and warehouses | Part-time, often involves scheduled inspections or follow-ups |
| Employer & Industry Usage | FDA, government agencies, regulated industries | FDA, contractors, or consulting firms |
Full Time Fda Inspectors work primarily on-site, conducting regular inspections and ensuring compliance with FDA regulations. Part Time Fda Inspectors perform inspections on a flexible schedule, often supplementing full-time staff. Both roles require similar credentials but differ mainly in hours and scope of work.
$60K - $76K/yr
Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 23 days ago
The Regulatory Affairs Specialist (FDA, DEA) will ensure BaRupOn's pharmacy, manufacturing, and healthcare operations meet all applicable regulatory requirements. This position is responsible for preparing submissions, maintaining licenses, coordinating audits, and staying ahead of evolving federal and state regulations related to pharmaceuticals, medical devices, and controlled substances.
Key Responsibilities