... pharmaceutical products in compliance with company policies and procedures, FDA regulations, and current Good Manufacturing Practices (cGMP). This role supports production and packaging operations ...
... pharmaceutical products in compliance with company policies and procedures, FDA regulations, and current Good Manufacturing Practices (cGMP). This role supports production and packaging operations ...
... pharmaceutical products in compliance with company policies and procedures, FDA regulations, and current Good Manufacturing Practices (cGMP). This role supports production and packaging operations ...
... pharmaceutical products in compliance with company policies and procedures, FDA regulations, and current Good Manufacturing Practices (cGMP). This role supports production and packaging operations ...
... pharmaceutical products in compliance with company policies and procedures, FDA regulations, and current Good Manufacturing Practices (cGMP). This role supports production and packaging operations ...
... pharmaceutical products in compliance with company policies and procedures, FDA regulations, and current Good Manufacturing Practices (cGMP). This role supports production and packaging operations ...
Support FDA inspections, regulatory audits, and customer audits. * Develop and maintain USP-related ... Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, Food Science, or a related ...
Support FDA inspections, regulatory audits, and customer audits. * Develop and maintain USP-related ... Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, Food Science, or a related ...
Senior FDA Attorney
Pine Brook, NJ · On-site +1
$250K - $400K/yr
Salary: $250,000 - $400,000 per year A bit about us: ----- Senior FDA Attorney Counsel or Senior ... inspection, and compliance obligations. Counsel bulk active pharmaceutical ingredient suppliers ...
Senior FDA Attorney
Pine Brook, NJ · On-site +1
$250K - $400K/yr
Salary: $250,000 - $400,000 per year A bit about us: ----- Senior FDA Attorney Counsel or Senior ... inspection, and compliance obligations. Counsel bulk active pharmaceutical ingredient suppliers ...
FDA Attorney
Pine Brook, NJ · On-site +1
In the Life Sciences, Firm X, has represented pharmacies of all kinds and assisted with regulatory ... FDA inspections, 483 responses and warning letters * Drug withdrawals and recalls * FDA importation ...
Quick apply
FDA Attorney
Pine Brook, NJ · On-site +1
In the Life Sciences, Firm X, has represented pharmacies of all kinds and assisted with regulatory ... FDA inspections, 483 responses and warning letters * Drug withdrawals and recalls * FDA importation ...
Director, Quality Compliance (DEA & FDA)
$180K - $220K/yr
... 000 base salary + bonus potential Position Summary A growing pharmaceutical manufacturing ... Lead inspection readiness programs and provide on-site support during regulatory inspections
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Director, Quality Compliance (DEA & FDA)
$180K - $220K/yr
... 000 base salary + bonus potential Position Summary A growing pharmaceutical manufacturing ... Lead inspection readiness programs and provide on-site support during regulatory inspections
FDA + Healthcare Regulatory Associate Attorney
$260K - $365K/yr
Pharmaceutical and biotechnology industries * Medical device and healthcare technology spaces ... FDA and USDA inspections * Remediation of inspection findings * Draft regulatory analyses, client ...
Quick apply
FDA + Healthcare Regulatory Associate Attorney
$260K - $365K/yr
Pharmaceutical and biotechnology industries * Medical device and healthcare technology spaces ... FDA and USDA inspections * Remediation of inspection findings * Draft regulatory analyses, client ...
FDA Technical Consultant
Washington, DC · On-site +1
... FDA inspections at pharmaceutical and medical device manufacturing sites. This role offers ... The salary range for this position in Washington D.C. is $200,000-$250,000 and represents the firm ...
FDA Technical Consultant
Washington, DC · On-site +1
... FDA inspections at pharmaceutical and medical device manufacturing sites. This role offers ... The salary range for this position in Washington D.C. is $200,000-$250,000 and represents the firm ...
FDA Technical Consultant
Washington, DC · On-site
... FDA inspections at pharmaceutical and medical device manufacturing sites. This role offers ... The salary range for this position in Washington D.C. is $200,000-$250,000 and represents the firm ...
FDA Technical Consultant
Washington, DC · On-site
... FDA inspections at pharmaceutical and medical device manufacturing sites. This role offers ... The salary range for this position in Washington D.C. is $200,000-$250,000 and represents the firm ...
Regulatory Affairs Specialist (FDA, DEA )
Irvine, CA · On-site
$60K - $76K/yr
Support internal audits, site inspections, and responses to 483s or warning letters * Coordinate ... in pharmaceuticals, biotech, or medical devices * Working knowledge of FDA regulations (21 CFR ...
Quick apply
Regulatory Affairs Specialist (FDA, DEA )
Irvine, CA · On-site
$60K - $76K/yr
Support internal audits, site inspections, and responses to 483s or warning letters * Coordinate ... in pharmaceuticals, biotech, or medical devices * Working knowledge of FDA regulations (21 CFR ...
Regulatory Affairs Specialist (FDA, DEA )
Irvine, CA · On-site
$60K - $76K/yr
Support internal audits, site inspections, and responses to 483s or warning letters * Coordinate ... in pharmaceuticals, biotech, or medical devices * Working knowledge of FDA regulations (21 CFR ...
Regulatory Affairs Specialist (FDA, DEA )
Irvine, CA · On-site
$60K - $76K/yr
Support internal audits, site inspections, and responses to 483s or warning letters * Coordinate ... in pharmaceuticals, biotech, or medical devices * Working knowledge of FDA regulations (21 CFR ...
Regulatory Affairs Specialist (FDA, DEA )
Irvine, CA · On-site
$60K - $76K/yr
Support internal audits, site inspections, and responses to 483s or warning letters * Coordinate ... in pharmaceuticals, biotech, or medical devices * Working knowledge of FDA regulations (21 CFR ...
Regulatory Affairs Specialist (FDA, DEA )
Irvine, CA · On-site
$60K - $76K/yr
Support internal audits, site inspections, and responses to 483s or warning letters * Coordinate ... in pharmaceuticals, biotech, or medical devices * Working knowledge of FDA regulations (21 CFR ...
Associate, FDA Regulations - DC
Washington, DC · On-site
$365K/yr
... pharmaceuticals, medical devices, biologics, health technologies, food, and cosmetics. Key ... Provide legal guidance during FDA inspections, investigations, and enforcement actions * Conduct ...
Associate, FDA Regulations - DC
Washington, DC · On-site
$365K/yr
... pharmaceuticals, medical devices, biologics, health technologies, food, and cosmetics. Key ... Provide legal guidance during FDA inspections, investigations, and enforcement actions * Conduct ...
Associate, FDA Regulations - DC
Washington, DC · On-site
$225K/yr
... pharmaceuticals, medical devices, biologics, health technologies, food, and cosmetics. Key ... Provide legal guidance during FDA inspections, investigations, and enforcement actions * Conduct ...
Associate, FDA Regulations - DC
Washington, DC · On-site
$225K/yr
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Pharmaceutical Engineer
Raleigh, NC · On-site
$120K - $145K/yr
Ensure all validation documentation complies with cGMP, FDA, ISPE, and GAMP guidelines ... Collaborate with Quality Assurance and Manufacturing teams to support inspection readiness and ...
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Pharmaceutical Engineer
Raleigh, NC · On-site
$120K - $145K/yr
Ensure all validation documentation complies with cGMP, FDA, ISPE, and GAMP guidelines ... Collaborate with Quality Assurance and Manufacturing teams to support inspection readiness and ...
Job Title: QA/QC Inspector - Biopharmaceutical Construction This role supports a major ... You will gain exposure to pharmaceutical quality systems, FDA-regulated documentation practices ...
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Job Title: QA/QC Inspector - Biopharmaceutical Construction This role supports a major ... You will gain exposure to pharmaceutical quality systems, FDA-regulated documentation practices ...
QA Inspector
West Palm Beach, FL · On-site
$18 - $24/hr
... pharmaceutical manufacturing * Knowledge of GMP, HACCP, SQF, or FDA regulations * Experience with raw material inspection strongly preferred * Ability to work in cold/freezer environments * Strong ...
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QA Inspector
West Palm Beach, FL · On-site
$18 - $24/hr
... pharmaceutical manufacturing * Knowledge of GMP, HACCP, SQF, or FDA regulations * Experience with raw material inspection strongly preferred * Ability to work in cold/freezer environments * Strong ...
Compounding Pharmaceutical QA/QC
Lake Charles, LA · On-site
$75K - $85K/yr
... inspection to final product release. The role requires meticulous attention to detail to identify ... In-depth knowledge of USP , USP , USP , and FDA regulations applicable to pharmaceutical ...
Quick apply
Compounding Pharmaceutical QA/QC
Lake Charles, LA · On-site
$75K - $85K/yr
... inspection to final product release. The role requires meticulous attention to detail to identify ... In-depth knowledge of USP , USP , USP , and FDA regulations applicable to pharmaceutical ...
PR · On-site
Salary: Previous Pharmaceutical/Biotech experience is mandatory for this role (Commissioning ... Experience supporting FDA audits and regulatory inspections. * Background in biologics, sterile ...
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PR · On-site
Salary: Previous Pharmaceutical/Biotech experience is mandatory for this role (Commissioning ... Experience supporting FDA audits and regulatory inspections. * Background in biologics, sterile ...
Fda Pharmaceutical Inspector Salary information
See salary details
$12.50 - $16.11
6% of jobs
$18.70 is the 25th percentile. Wages below this are outliers.
$16.11 - $19.71
26% of jobs
The median wage is $23.21 / hr.
$19.71 - $23.32
18% of jobs
$23.32 - $26.92
14% of jobs
$29.43 is the 75th percentile. Wages above this are outliers.
$26.92 - $30.53
15% of jobs
$30.53 - $34.13
6% of jobs
$34.13 - $37.74
4% of jobs
$37.74 - $41.35
4% of jobs
$41.35 - $44.95
1% of jobs
$44.95 - $48.56
3% of jobs
$48.56 - $52.16
1% of jobs
$12
$27
$52
How much do fda pharmaceutical inspector salary jobs pay per hour?
What is the difference between Fda Pharmaceutical Inspector Salary vs Fda Food Inspector Salary?
| Factor | Fda Pharmaceutical Inspector Salary | Fda Food Inspector Salary |
|---|---|---|
| Required Credentials | Bachelor's degree in pharmacy, chemistry, or related field; often requires FDA-specific training | Bachelor's degree in food science, biology, or related field; FDA training may be needed |
| Work Environment | Inspecting pharmaceutical manufacturing facilities, laboratories, and compliance sites | Inspecting food processing plants, warehouses, and retail outlets |
| Employer & Industry Usage | U.S. Food and Drug Administration, pharmaceutical industry | U.S. Food and Drug Administration, food industry |
While both roles involve regulatory inspections within the FDA, Fda Pharmaceutical Inspectors typically focus on pharmaceutical manufacturing and require specialized knowledge in drugs and chemistry. Fda Food Inspectors concentrate on food safety and inspection of food production facilities. Salary differences depend on industry demand, specialization, and experience.

Full-time
Re-posted 10 days ago
Job description
The Production Visual Inspector is responsible for performing visual inspection activities for injectable and ophthalmic pharmaceutical products in compliance with company policies and procedures, FDA regulations, and current Good Manufacturing Practices (cGMP). This role supports production and packaging operations while maintaining accurate documentation, ensuring product quality, and promoting a safe and compliant work environment.
Essential Duties and Responsibilities:
• Perform 100% visual inspection of ophthalmic and parenteral drug products, including vials, syringes, ampoules, bottles, and IV bags, in accordance with cGMP requirements and approved inspection procedures
• Inspect products for particulate matter, cosmetic defects, container closure integrity defects, fill level discrepancies, discoloration, cracks, chips, leaks, and other non-conformances
• Execute manual and semi-automated visual inspection activities while maintaining inspection qualification standards and inspection rate requirements
• Maintain compliance with current Good Manufacturing Practices (cGMP), FDA regulations, SOPs, batch records, and data integrity requirements
• Document inspection activities accurately and contemporaneously in batch records, logbooks, and electronic system
• Support line clearance, room setup, and inspection area readiness activities prior to production operations
• Identify, segregate, and report defective or non-conforming materials in accordance with quality procedures
• Participate in initial and annual visual inspection qualification and requalification programs, including defect kit training and certification activities
• Support investigations related to visual defects, deviations, complaints, and non-conforming product event
• Collaborate with Manufacturing, Quality Assurance, and Quality Control teams to ensure product quality and inspection compliance
• Assist with cleaning and sanitization of inspection equipment and work areas in controlled manufacturing environments
• Support continuous improvement initiatives related to inspection processes, defect reduction, and operational efficiency
• Participate in regulatory inspection readiness activities and provide documentation support during audits and inspections
• Follow all safety, gowning, contamination control, and aseptic behavior requirements while working in classified manufacturing environments
Education / Experience:
• High school diploma or GED required; Associate degree or Bachelor's degree in a scientific or technical field preferred
• Experience working with ophthalmic, sterile, injectable, or parenteral products preferred
• Knowledge of cGMP regulations, GDP documentation practices, and FDA pharmaceutical manufacturing requirements preferred
• Ability to identify visual defects and maintain visual acuity and visual inspection qualification standards required
• Experience working in controlled manufacturing environments preferred
• Strong attention to detail, manual dexterity, and ability to maintain concentration during repetitive inspection activities required
Working Conditions / Physical Requirements:
• Position requires bending (desk to floor), lifting (up to 15 lbs.), corrected vision (20/20), standing, sitting, typing, and walking.
• Ability to maintain concentration during repetitive inspection activities required.
About Nephron Pharmaceuticals
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
501 - 1,000 Employees
Headquarters location
West Columbia, SC, US
Year founded
1997