Participate in Mock inspections for FDA inspection preparation Qualifications Ability to work independently with little or no supervision Exeptional oral and written communication capabilities ...
Participate in Mock inspections for FDA inspection preparation Qualifications Ability to work independently with little or no supervision Exeptional oral and written communication capabilities ...
Participate in Mock inspections for FDA inspection preparation Qualifications Ability to work independently with little or no supervision Exeptional oral and written communication capabilities ...
Participate in Mock inspections for FDA inspection preparation Qualifications Ability to work independently with little or no supervision Exeptional oral and written communication capabilities ...
QC Lab Technician
$20 - $21/hr
... FDA-regulated micronization facility. This position involves monitoring production processes, conducting inspections, and collaborating with cross-functional teams to maintain high standards.
QC Lab Technician
$20 - $21/hr
... FDA-regulated micronization facility. This position involves monitoring production processes, conducting inspections, and collaborating with cross-functional teams to maintain high standards.
QC Lab Technician
Moorestown, NJ ยท On-site
$20 - $21/hr
Collaborate with the Quality Assurance team to address non-conformities. * Assist during internal and external audits, including FDA inspections. * Ensure compliance with cGMP (current Good ...
QC Lab Technician
Moorestown, NJ ยท On-site
$20 - $21/hr
Collaborate with the Quality Assurance team to address non-conformities. * Assist during internal and external audits, including FDA inspections. * Ensure compliance with cGMP (current Good ...
Senior Quality Inspector - CMM & Metrology | Up to $32/hr
Hatboro, PA ยท On-site
$26 - $32/hr
Document inspection results clearly and accurately according to Good Documentation Practices , ISO 13485, AS9100, FDA, and internal quality system requirements. * Support nonconformance reporting ...
Senior Quality Inspector - CMM & Metrology | Up to $32/hr
Hatboro, PA ยท On-site
$26 - $32/hr
Document inspection results clearly and accurately according to Good Documentation Practices , ISO 13485, AS9100, FDA, and internal quality system requirements. * Support nonconformance reporting ...
Support Charter Medical and Polyzen Customer Audits, ISO 13485 Audits and FDA Inspections to help defend the Software Validation Program. * Responsible for managing consultants on large projects with ...
Quick apply
Support Charter Medical and Polyzen Customer Audits, ISO 13485 Audits and FDA Inspections to help defend the Software Validation Program. * Responsible for managing consultants on large projects with ...
Support Charter Medical and Polyzen Customer Audits, ISO 13485 Audits and FDA Inspections to help defend the Software Validation Program. * Responsible for managing consultants on large projects with ...
Support Charter Medical and Polyzen Customer Audits, ISO 13485 Audits and FDA Inspections to help defend the Software Validation Program. * Responsible for managing consultants on large projects with ...
... FDA and other government and safety regulations by performing the following duties. Major Job ... Perform line clearance, inspections, and physical testing. Identify, investigate, and prepare ...
... FDA and other government and safety regulations by performing the following duties. Major Job ... Perform line clearance, inspections, and physical testing. Identify, investigate, and prepare ...
Food and Drug Administration (FDA) regulations, Company policies and operating procedures, and ... perform inspections in accordance with authorized specification and quality control standards.
Food and Drug Administration (FDA) regulations, Company policies and operating procedures, and ... perform inspections in accordance with authorized specification and quality control standards.
Food and Drug Administration (FDA) regulations, Company policies and operating procedures, and ... perform inspections in accordance with authorized specification and quality control standards.
Food and Drug Administration (FDA) regulations, Company policies and operating procedures, and ... perform inspections in accordance with authorized specification and quality control standards.
Food and Drug Administration (FDA) regulations, Company policies and operating procedures, and ... perform inspections in accordance with authorized specification and quality control standards.
Food and Drug Administration (FDA) regulations, Company policies and operating procedures, and ... perform inspections in accordance with authorized specification and quality control standards.
Food and Drug Administration (FDA) regulations, Company policies and operating procedures, and ... perform inspections in accordance with authorized specification and quality control standards.
Food and Drug Administration (FDA) regulations, Company policies and operating procedures, and ... perform inspections in accordance with authorized specification and quality control standards.
Assistant Food Safety & Kitchen Manager
Wilmington, DE ยท On-site
$28 - $30/hr
FDA inspections * Third-party audits (as applicable) * Manage food safety software systems to: * Trace incoming ingredients * Track lot codes and batch production * Enable full product traceability ...
Quick apply
Assistant Food Safety & Kitchen Manager
Wilmington, DE ยท On-site
$28 - $30/hr
FDA inspections * Third-party audits (as applicable) * Manage food safety software systems to: * Trace incoming ingredients * Track lot codes and batch production * Enable full product traceability ...
Validation Specialist II
Telford, PA ยท On-site
Support Charter Medical and Polyzen Customer Audits, ISO 13485 Audits and FDA Inspections to help defend the Software Validation Program. * Responsible for managing consultants on large projects with ...
Validation Specialist II
Telford, PA ยท On-site
Support Charter Medical and Polyzen Customer Audits, ISO 13485 Audits and FDA Inspections to help defend the Software Validation Program. * Responsible for managing consultants on large projects with ...
Validation Specialist II
Telford, PA ยท On-site
Support Charter Medical and Polyzen Customer Audits, ISO 13485 Audits and FDA Inspections to help defend the Software Validation Program. * Responsible for managing consultants on large projects with ...
Validation Specialist II
Telford, PA ยท On-site
Support Charter Medical and Polyzen Customer Audits, ISO 13485 Audits and FDA Inspections to help defend the Software Validation Program. * Responsible for managing consultants on large projects with ...
The QC inspector will also be responsible for ensuring all policies and procedures are in compliance with applicable FDA, state, OSHA, AATB, and ISO regulations and standards. Essential Functions:
The QC inspector will also be responsible for ensuring all policies and procedures are in compliance with applicable FDA, state, OSHA, AATB, and ISO regulations and standards. Essential Functions:
QA Inspector - 3rd shift
Conshohocken, PA ยท On-site
The impact of the quality inspection process directly impacts company compliance to regulatory ... General knowledge of FDA regulations related to cGMPs is desired. General knowledge of quality ...
QA Inspector - 3rd shift
Conshohocken, PA ยท On-site
The impact of the quality inspection process directly impacts company compliance to regulatory ... General knowledge of FDA regulations related to cGMPs is desired. General knowledge of quality ...
QA Inspector - 3rd shift
Conshohocken, PA ยท On-site
The impact of the quality inspection process directly impacts company compliance to regulatory ... General knowledge of FDA regulations related to cGMPs is desired. General knowledge of quality ...
QA Inspector - 3rd shift
Conshohocken, PA ยท On-site
The impact of the quality inspection process directly impacts company compliance to regulatory ... General knowledge of FDA regulations related to cGMPs is desired. General knowledge of quality ...
QA Inspector - 3rd shift
Conshohocken, PA ยท On-site
The impact of the quality inspection process directly impacts company compliance to regulatory ... General knowledge of FDA regulations related to cGMPs is desired. General knowledge of quality ...
QA Inspector - 3rd shift
Conshohocken, PA ยท On-site
The impact of the quality inspection process directly impacts company compliance to regulatory ... General knowledge of FDA regulations related to cGMPs is desired. General knowledge of quality ...
Digital Systems Validation Lead
Wayne, PA ยท Hybrid
$116K - $130K/yr
Familiarity supporting FDA inspections, notified body reviews, and internal or external quality audits * Understanding of SDLC and Agile development environments and how validation integrates within ...
Digital Systems Validation Lead
Wayne, PA ยท Hybrid
$116K - $130K/yr
Familiarity supporting FDA inspections, notified body reviews, and internal or external quality audits * Understanding of SDLC and Agile development environments and how validation integrates within ...
Fda Inspector information
See Philadelphia, PA salary details
$24.7K - $31.6K
3% of jobs
$31.6K - $38.4K
16% of jobs
$40.1K is the 25th percentile. Wages below this are outliers.
$38.4K - $45.2K
23% of jobs
The median wage is $47.3K / yr.
$45.2K - $52.1K
27% of jobs
$56.4K is the 75th percentile. Wages above this are outliers.
$52.1K - $58.9K
10% of jobs
$58.9K - $65.7K
4% of jobs
$65.7K - $72.6K
5% of jobs
$72.6K - $79.4K
2% of jobs
$79.4K - $86.2K
2% of jobs
$86.2K - $93.1K
2% of jobs
$93.1K - $99.9K
5% of jobs
$24.7K
$55.4K
$99.9K
How much do fda inspector jobs pay per year?
How much do FDA drug investigators make?
What types of facilities or products do FDA Inspectors typically 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.
What are the key skills and qualifications needed to thrive in the Fda Inspector position, and why are they important?
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 type of inspector gets paid the most?
Is it hard to get a job at FDA?
How do you become an FDA inspector?
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.
Full-time
Posted 18 days ago
Key responsibilities
Write and review SOPs, technical data forms, and quality documents related to quality assurance.
Assist in carrying out internal quality audits and perform investigations on non-conformances and customer complaints.
Maintain control documents in Quality Assurance and ensure their distribution to different departments.
Job description
Our clientis a medical device company dedicated to offering innovative solutions for treatment of chronic heart failure. The Company's developments are based on its proprietary technology for administrating Cardiac Contractility Modulation therapy.
Job Description
- Write and review of SOPs and other quality assiuance related technical data forms and quality documents
- proper maintenance of control documents in Quality Assurance
- Control documents to differents departments
- Review validation protocols for GMP compliance
- Assist in carrying out internal quality audits on company systems and documentations
- perform investigations on non-conformances and customer complaint close out and corrective actions
- Audit on-going vendors, systems and documents to assure quality assurance compliance with regard to all internal procedures as well as regulatory guidelines
- Provide GCP/ QA support and avdvice to internal and external clients
- Ensure the timely and effective follow up to all identified or assigned quality issues
- Maintains and demonstrates understanding of global standards, regulation and regulatory bodies to include but not limited to ISO13485, 21FR; part 820 AIMD
- Assist in the maintenance ogf Quality Management System under direction of Director, Quality Assurance
- Participate in Mock inspections for FDA inspection preparation
Qualifications
Ability to work independently with little or no supervision
Exeptional oral and written communication capabilities
Advance computer knowledge in MS Office programs
Bachelors's Dregree in related field
4-6 years related experience
Experience working in regulated environment with medical devices
Experience with FDA inspections and /or Notified Bodies Audits desirable
Additional Information
All your information will be kept confidential according to EEO guidelines.