... inspections and audits, reviewing documentation, and ensuring all activities adhere to regulatory standards, including FDA, DEA, and ISO 17025 requirements. This role requires close collaboration ...
... inspections and audits, reviewing documentation, and ensuring all activities adhere to regulatory standards, including FDA, DEA, and ISO 17025 requirements. This role requires close collaboration ...
... inspections and audits, reviewing documentation, and ensuring all activities adhere to regulatory standards, including FDA, DEA, and ISO 17025 requirements. This role requires close collaboration ...
... inspections and audits, reviewing documentation, and ensuring all activities adhere to regulatory standards, including FDA, DEA, and ISO 17025 requirements. This role requires close collaboration ...
... inspections and audits by agencies such as FDA, EMA, and Notified Bodies. Act as a liaison with regulatory authorities during inspections, responding to queries and providing necessary documentation ...
... inspections and audits by agencies such as FDA, EMA, and Notified Bodies. Act as a liaison with regulatory authorities during inspections, responding to queries and providing necessary documentation ...
... inspections and audits by agencies such as FDA, EMA, and Notified Bodies. Act as a liaison with regulatory authorities during inspections, responding to queries and providing necessary documentation ...
... inspections and audits by agencies such as FDA, EMA, and Notified Bodies. Act as a liaison with regulatory authorities during inspections, responding to queries and providing necessary documentation ...
... inspections and audits by agencies such as FDA, EMA, and Notified Bodies Act as a liaison with regulatory authorities during inspections, responding to queries and providing necessary documentation ...
... inspections and audits by agencies such as FDA, EMA, and Notified Bodies Act as a liaison with regulatory authorities during inspections, responding to queries and providing necessary documentation ...
Manufacturing Assembler / Production Technician
Irving, TX · On-site
$15.25 - $18.50/hr
Inspect incoming components and finished products for compliance with FDA, ISO, and internal quality standards. * Troubleshoot production issues and collaborate with Engineering, Quality, and Product ...
Quick apply
Manufacturing Assembler / Production Technician
Irving, TX · On-site
$15.25 - $18.50/hr
Inspect incoming components and finished products for compliance with FDA, ISO, and internal quality standards. * Troubleshoot production issues and collaborate with Engineering, Quality, and Product ...
Maintains all QA documents necessary to exceed Annual FDA Inspection requirements. * Is responsible for obtaining and maintaining ACR accreditation. Exceptional compensation for the right candidate!
Quick apply
Maintains all QA documents necessary to exceed Annual FDA Inspection requirements. * Is responsible for obtaining and maintaining ACR accreditation. Exceptional compensation for the right candidate!
QA Specialist I
Plano, TX · On-site
... Record inspection and test data as instructed. • Recommend changes to policies and procedures. • Document non-conformances in the Non-Conforming Material Review system. • Comply with FDA ...
Quick apply
QA Specialist I
Plano, TX · On-site
... Record inspection and test data as instructed. • Recommend changes to policies and procedures. • Document non-conformances in the Non-Conforming Material Review system. • Comply with FDA ...
Ensure IT systems comply with GxP, FDA 21 CFR Part 11, and data integrity requirements. Participate ... Support audits and inspections as needed. Required Qualifications Bachelor's degree in Computer ...
Quick apply
Ensure IT systems comply with GxP, FDA 21 CFR Part 11, and data integrity requirements. Participate ... Support audits and inspections as needed. Required Qualifications Bachelor's degree in Computer ...
Ensure IT systems comply with GxP, FDA 21 CFR Part 11, and data integrity requirements. Participate ... Support audits and inspections as needed. Required Qualifications Bachelor's degree in Computer ...
Quick apply
Ensure IT systems comply with GxP, FDA 21 CFR Part 11, and data integrity requirements. Participate ... Support audits and inspections as needed. Required Qualifications Bachelor's degree in Computer ...
Quality Systems Specialist III
Plano, TX · On-site
$75K - $91K/yr
Coordinate and prepare for internal and external regulatory inspections and audits (ISO 13485, FDA, Notified Body, Competent Authorities, etc.). * Set up and lead backroom activities to provide ...
Quality Systems Specialist III
Plano, TX · On-site
$75K - $91K/yr
Coordinate and prepare for internal and external regulatory inspections and audits (ISO 13485, FDA, Notified Body, Competent Authorities, etc.). * Set up and lead backroom activities to provide ...
Quality Systems Specialist III
Plano, TX · On-site
$75K - $91K/yr
Coordinate and prepare for internal and external regulatory inspections and audits (ISO 13485, FDA, Notified Body, Competent Authorities, etc.). * Set up and lead backroom activities to provide ...
Quick apply
Quality Systems Specialist III
Plano, TX · On-site
$75K - $91K/yr
Coordinate and prepare for internal and external regulatory inspections and audits (ISO 13485, FDA, Notified Body, Competent Authorities, etc.). * Set up and lead backroom activities to provide ...
Coordinate and prepare for internal and external regulatory inspections and audits (ISO 13485, FDA, Notified Body, Competent Authorities, etc.). * Set up and lead backroom activities to provide ...
Coordinate and prepare for internal and external regulatory inspections and audits (ISO 13485, FDA, Notified Body, Competent Authorities, etc.). * Set up and lead backroom activities to provide ...
Quality Systems Specialist III
$75K - $91K/yr
Coordinate and prepare for internal and external regulatory inspections and audits (ISO 13485, FDA, Notified Body, Competent Authorities, etc.). * Set up and lead backroom activities to provide ...
Quality Systems Specialist III
$75K - $91K/yr
Coordinate and prepare for internal and external regulatory inspections and audits (ISO 13485, FDA, Notified Body, Competent Authorities, etc.). * Set up and lead backroom activities to provide ...
Quality Systems Specialist III
$75K - $91K/yr
Coordinate and prepare for internal and external regulatory inspections and audits (ISO 13485, FDA, Notified Body, Competent Authorities, etc.). * Set up and lead backroom activities to provide ...
Quality Systems Specialist III
$75K - $91K/yr
Coordinate and prepare for internal and external regulatory inspections and audits (ISO 13485, FDA, Notified Body, Competent Authorities, etc.). * Set up and lead backroom activities to provide ...
Ensure all investigations comply with FDA guidance, cGMPs, and expectations for sterile drug ... Support audit readiness and provide SME support during regulatory inspections as needed. Retest and ...
Ensure all investigations comply with FDA guidance, cGMPs, and expectations for sterile drug ... Support audit readiness and provide SME support during regulatory inspections as needed. Retest and ...
Ensure compliance with GMP & FDA 21 CFR Part 11 (audit trails, electronic records, RBAC). * Support ... Support audit readiness and regulatory inspections. Required Skills & Expertise OT & Automation
Ensure compliance with GMP & FDA 21 CFR Part 11 (audit trails, electronic records, RBAC). * Support ... Support audit readiness and regulatory inspections. Required Skills & Expertise OT & Automation
Operator I
Irving, TX · On-site
$17/hr
Inspect components and finished products for compliance with FDA and ISO standards. * Troubleshoot production issues and collaborate with engineering, quality, and product development teams.
Quick apply
Operator I
Irving, TX · On-site
$17/hr
Inspect components and finished products for compliance with FDA and ISO standards. * Troubleshoot production issues and collaborate with engineering, quality, and product development teams.
Responsible for annual inspection by TDH and FDA. Attend monthly departmental staff meetings. Responsible for completing quarterly QI report for QRMC. Non-Direct Patient Care: * Documentation:
Responsible for annual inspection by TDH and FDA. Attend monthly departmental staff meetings. Responsible for completing quarterly QI report for QRMC. Non-Direct Patient Care: * Documentation:
Mammographer PRN Burleson
Fort Worth, TX · On-site
Responsible for annual inspection by TDH and FDA. Attend monthly departmental staff meetings. Responsible for completing quarterly QI report for QRMC. Non-Direct Patient Care: * Documentation:
Mammographer PRN Burleson
Fort Worth, TX · On-site
Responsible for annual inspection by TDH and FDA. Attend monthly departmental staff meetings. Responsible for completing quarterly QI report for QRMC. Non-Direct Patient Care: * Documentation:
Fda Inspector information
See Dallas, TX salary details
$24.3K - $31.1K
3% of jobs
$31.1K - $37.8K
16% of jobs
$39.5K is the 25th percentile. Wages below this are outliers.
$37.8K - $44.5K
23% of jobs
The median wage is $46.5K / yr.
$44.5K - $51.3K
27% of jobs
$55.6K is the 75th percentile. Wages above this are outliers.
$51.3K - $58K
10% of jobs
$58K - $64.7K
4% of jobs
$64.7K - $71.4K
5% of jobs
$71.4K - $78.2K
2% of jobs
$78.2K - $84.9K
2% of jobs
$84.9K - $91.6K
2% of jobs
$91.6K - $98.4K
5% of jobs
$24.3K
$54.6K
$98.4K
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.
- Draw Inspector
- Ndt Quality Control Inspector
- Full Time Mueller Reports Property Inspector
- Visual Dimensional Inspector
- Quality Assurance Quality Inspector
- Quality Control Cmm Inspector
- Quality Consulting
- Entrylevel Quality Control Inspector
- Director Football Quality Control Coach
- Insulation Quality Control Inspector
Full-time
Medical, Dental, Vision, PTO
Posted 13 days ago
Job description
Pharmaceutical GMP QA Specialist
Synergy is seeking a detail-oriented and experienced Pharmaceutical GMP QA Specialist to ensure compliance with Good Manufacturing Practices (GMP) in pharmaceutical development and testing processes. The QA Specialist will be responsible for implementing and maintaining quality management systems, conducting inspections and audits, reviewing documentation, and ensuring all activities adhere to regulatory standards, including FDA, DEA, and ISO 17025 requirements. This role requires close collaboration with the development and testing teams to maintain compliance with the regulatory requirements.
Key Responsibilities:
- Ensure adherence to pharmaceutical GMP regulations and internal quality standards.
- Conduct routine and for-cause internal audits and inspections of chemistry, microbiology, and molecular biology laboratories.
- Review and approve GMP-related documentation, including test results, technical reports, investigation reports, and SOPs.
- Coordinate with cross-functional teams to address non-conformities and implement corrective and preventive actions (CAPAs).
- Support regulatory inspections and manage responses to audit findings.
- Monitor quality metrics and report on compliance status.
- Provide training and guidance on GMP requirements to laboratory personnel.
Education & Experience:
- Bachelor's degree in Chemistry or Microbiology.
- Minimum 10 years of experience in pharmaceutical quality assurance with strong knowledge of GMP regulations.
- Experience working within the FDA, DEA, and ISO 17025.
- Proven ability to conduct audits and manage quality documentation.
- Strong communication, analytical, and interpersonal skills.
Requirements
Education:
- Bachelor's degree in Chemistry or Microbiology.
Experience:
- 10 + years of experience in pharmaceutical quality assurance or GMP compliance.
- Familiarity with the FDA, DEA, and the iSO 17025 regulations and requirements.
- Experience in conducting audits and managing quality systems.
Skills:
- Strong analytical and problem-solving abilities.
- Excellent communication and interpersonal skills.
- Ability to work collaboratively in cross-functional teams.
Benefits
- Health Care Plan (Medical, Dental & Vision)
- Paid Time Off (Vacation, Sick & Public Holidays)
- Training & Development
About Synergy BIS
Sourced by ZipRecruiter
Company size
501 - 1,000 Employees
Headquarters location
Reston, VA, US
Year founded
2005