Production Quality Auditor
$17 - $20/hr
Knowledge of Quality Management Systems (ISO,FDA, BSI) is preferred. * Knowledge of Flexographic and/or digital printing or previous experience as a Quality Auditor is preferred. Pay: $17.00-20.00 ...
$17 - $20/hr
Knowledge of Quality Management Systems (ISO,FDA, BSI) is preferred. * Knowledge of Flexographic and/or digital printing or previous experience as a Quality Auditor is preferred. Pay: $17.00-20.00 ...
$17 - $20/hr
Knowledge of Quality Management Systems (ISO,FDA, BSI) is preferred. * Knowledge of Flexographic and/or digital printing or previous experience as a Quality Auditor is preferred. Pay: $17.00-20.00 ...
Sanford, FL · On-site
$17 - $20/hr
Knowledge of Quality Management Systems (ISO,FDA, BSI) is preferred. * Knowledge of Flexographic and/or digital printing or previous experience as a Quality Auditor is preferred. Pay: $17.00-20.00 ...
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Sanford, FL · On-site
$17 - $20/hr
Knowledge of Quality Management Systems (ISO,FDA, BSI) is preferred. * Knowledge of Flexographic and/or digital printing or previous experience as a Quality Auditor is preferred. Pay: $17.00-20.00 ...
Sanford, FL · On-site
$17 - $20/hr
Knowledge of Quality Management Systems (ISO,FDA, BSI) is preferred. * Knowledge of Flexographic and/or digital printing or previous experience as a Quality Auditor is preferred. Pay: $17.00-20.00 ...
Sanford, FL · On-site
$17 - $20/hr
Knowledge of Quality Management Systems (ISO,FDA, BSI) is preferred. * Knowledge of Flexographic and/or digital printing or previous experience as a Quality Auditor is preferred. Pay: $17.00-20.00 ...
... FDA), Good Clinical Practice (GCP), and other federal regulations, International Council for ... auditing. Experience: Minimum 1 (preferably 2 years) of research-related experience, including ...
... FDA), Good Clinical Practice (GCP), and other federal regulations, International Council for ... auditing. Experience: Minimum 1 (preferably 2 years) of research-related experience, including ...
... FDA), Good Clinical Practice (GCP), and other federal regulations, International Council for ... auditing. Experience: Minimum 1 (preferably 2 years) of research-related experience, including ...
... FDA), Good Clinical Practice (GCP), and other federal regulations, International Council for ... auditing. Experience: Minimum 1 (preferably 2 years) of research-related experience, including ...
Lakeland, FL · On-site
$17.75 - $23.50/hr
... FDA regulations including, but not limited to traceability records, temperature monitoring and ... auditing and updating the plant reference book * conducting data entry and * ensuring that all ...
Lakeland, FL · On-site
$17.75 - $23.50/hr
... FDA regulations including, but not limited to traceability records, temperature monitoring and ... auditing and updating the plant reference book * conducting data entry and * ensuring that all ...
Fort Lauderdale, FL · On-site
$36K - $43K/yr
Auditing & Compliance * Perform routine internal audits of inventory, warehouse operations, and documentation. * Ensure compliance with company policies, FDA regulations, and medical device industry ...
Fort Lauderdale, FL · On-site
$36K - $43K/yr
Auditing & Compliance * Perform routine internal audits of inventory, warehouse operations, and documentation. * Ensure compliance with company policies, FDA regulations, and medical device industry ...
... FDA, USDA and 3rd party auditors) which can include accompanying the auditor and corrective action plan follow up * interaction with plant management which includes assisting departments in ...
... FDA, USDA and 3rd party auditors) which can include accompanying the auditor and corrective action plan follow up * interaction with plant management which includes assisting departments in ...
Review of FDA submissions. * Assist/work with consultants as needed. * Support R&D with 510(k ... Fulfill the role of internal auditor. Also, manage the Internal Audit Program. * Prepare supplier ...
Review of FDA submissions. * Assist/work with consultants as needed. * Support R&D with 510(k ... Fulfill the role of internal auditor. Also, manage the Internal Audit Program. * Prepare supplier ...
Review of FDA submissions. * Assist/work with consultants as needed. * Support R&D with 510(k ... Fulfill the role of internal auditor. Also, manage the Internal Audit Program. * Prepare supplier ...
Review of FDA submissions. * Assist/work with consultants as needed. * Support R&D with 510(k ... Fulfill the role of internal auditor. Also, manage the Internal Audit Program. * Prepare supplier ...
... auditing, and risk management activities with respect to global regulatory requirements and MDSAP (FDA, ISO, EU MDR, ANVISA, MHLW, and TGA). General Duties and Responsibilities : * Ensure the ongoing ...
... auditing, and risk management activities with respect to global regulatory requirements and MDSAP (FDA, ISO, EU MDR, ANVISA, MHLW, and TGA). General Duties and Responsibilities : * Ensure the ongoing ...
Auburndale, FL · On-site
$61K - $79K/yr
Working knowledge of FSSC 22000 or SQF, HACCP, GMPs, FDA food regulations, internal auditing, and document control. * Demonstrated experience with root cause analysis, CAPA, data analysis, and ...
Auburndale, FL · On-site
$61K - $79K/yr
Working knowledge of FSSC 22000 or SQF, HACCP, GMPs, FDA food regulations, internal auditing, and document control. * Demonstrated experience with root cause analysis, CAPA, data analysis, and ...
Authors US FDA premarket submissions (e.g., 510(k), Q-submissions) and international submissions ... Participates in audits by regulatory authorities, certification bodies, or internal auditors.
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Authors US FDA premarket submissions (e.g., 510(k), Q-submissions) and international submissions ... Participates in audits by regulatory authorities, certification bodies, or internal auditors.
Authors US FDA premarket submissions (e.g., 510(k), Q-submissions) and international submissions ... Participates in audits by regulatory authorities, certification bodies, or internal auditors.
Authors US FDA premarket submissions (e.g., 510(k), Q-submissions) and international submissions ... Participates in audits by regulatory authorities, certification bodies, or internal auditors.
Ponte Vedra, FL · On-site +1
Authors US FDA premarket submissions (e.g., 510(k), Q-submissions) and international submissions ... Participates in audits by regulatory authorities, certification bodies, or internal auditors.
Ponte Vedra, FL · On-site +1
Authors US FDA premarket submissions (e.g., 510(k), Q-submissions) and international submissions ... Participates in audits by regulatory authorities, certification bodies, or internal auditors.
Naples, FL · On-site
$100 - $130/hr
Quality System Leadership Lead and oversee the end-to-end QMS, ensuring compliance with FDA, ISO ... Drive capability development in auditing, compliance, and quality system processes. Education and ...
Naples, FL · On-site
$100 - $130/hr
Quality System Leadership Lead and oversee the end-to-end QMS, ensuring compliance with FDA, ISO ... Drive capability development in auditing, compliance, and quality system processes. Education and ...
Davie, FL · On-site
Excellent working knowledge of the FDA's 21 CFR Part 820; ISO 13485; EU Medical Device Directive ... Certified Lead Auditor or ASQ certification as a Certified Quality Auditor (CQA), Certified Quality ...
Davie, FL · On-site
Excellent working knowledge of the FDA's 21 CFR Part 820; ISO 13485; EU Medical Device Directive ... Certified Lead Auditor or ASQ certification as a Certified Quality Auditor (CQA), Certified Quality ...
Naples, FL · On-site
Quality System Leadership Lead and oversee the end-to-end QMS, ensuring compliance with FDA, ISO ... development in auditing, compliance, and quality system processes Education and Experience:
Naples, FL · On-site
Quality System Leadership Lead and oversee the end-to-end QMS, ensuring compliance with FDA, ISO ... development in auditing, compliance, and quality system processes Education and Experience:
Naples, FL · On-site
Quality System Leadership Lead and oversee the end-to-end QMS, ensuring compliance with FDA, ISO ... development in auditing, compliance, and quality system processes Education and Experience:
Naples, FL · On-site
Quality System Leadership Lead and oversee the end-to-end QMS, ensuring compliance with FDA, ISO ... development in auditing, compliance, and quality system processes Education and Experience:
Seminole, FL · On-site
$85K - $87K/yr
Participate in internal and regulatory facility audits (e.g., FDA inspections) and ensure the laboratory remains audit-ready at all time * Lab Infrastructure & Auditing: Maintain an audit-ready ...
Seminole, FL · On-site
$85K - $87K/yr
Participate in internal and regulatory facility audits (e.g., FDA inspections) and ensure the laboratory remains audit-ready at all time * Lab Infrastructure & Auditing: Maintain an audit-ready ...
$24.7K - $30.7K
2% of jobs
$30.7K - $36.7K
17% of jobs
$39.8K is the 25th percentile. Wages below this are outliers.
$36.7K - $42.7K
12% of jobs
$42.7K - $48.7K
11% of jobs
The median wage is $51.9K / yr.
$48.7K - $54.7K
17% of jobs
$54.7K - $60.7K
7% of jobs
$60.7K - $66.7K
6% of jobs
$66.7K - $72.8K
3% of jobs
$72.9K is the 75th percentile. Wages above this are outliers.
$72.8K - $78.8K
17% of jobs
$78.8K - $84.8K
4% of jobs
$84.8K - $90.8K
4% of jobs
$24.7K
$57K
$90.8K
An FDA Auditor is responsible for inspecting facilities, processes, and documentation to ensure compliance with U.S. Food and Drug Administration (FDA) regulations. They review manufacturing practices, quality control systems, and regulatory filings for industries such as pharmaceuticals, medical devices, and food production. FDA Auditors may work for the FDA or for companies preparing for FDA inspections. Their role helps ensure public safety by verifying that products meet legal and quality standards.
To thrive as an FDA Auditor, you need a strong background in life sciences, regulatory compliance, and audit methodologies, usually supported by a relevant degree and professional certifications such as RAC or CQA. Familiarity with FDA regulations (such as 21 CFR), electronic quality management systems (eQMS), and audit management tools is essential. Attention to detail, critical thinking, and strong communication skills help auditors navigate complex regulatory settings and interact effectively with stakeholders. These competencies are crucial for ensuring companies meet rigorous FDA standards and maintain regulatory compliance.
FDA Auditors often encounter challenges such as interpreting complex and evolving regulatory guidelines, managing on-site audits in diverse environments, and reviewing extensive documentation under tight timeframes. They must adapt quickly to various industry settings, handle potentially uncooperative stakeholders, and maintain objectivity throughout their evaluations. Successfully overcoming these challenges requires resilience, up-to-date regulatory knowledge, and excellent people skills. These hurdles are a vital part of ensuring public health and safety by holding organizations to the highest standards of compliance.
The most popular types of Fda Auditor jobs in Florida are:
For Fda Auditor jobs in Florida, the most frequently searched job titles are:
The top searched job categories for Fda Auditor jobs in Florida are:
Cities in Florida with the most Fda Auditor job openings:

Sanford, FL
$17 - $20/hr
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 18 days ago
Overview: The Production Quality Auditor monitors the quality performance of the production staff by completing quality audits at the beginning of each run and periodically throughout the run. They also work directly with the Quality Manager to identify, mitigate and improve quality performance by documenting and training on procedural changes to the Quality Management System (QMS).
Education & Experience Requirements:
Pay: $17.00-20.00/hour based on experience
Shift: Friday, Saturday 6:00pm-6:00am & Sunday 6:00pm-5:30am.
Training: TBD.
Benefits:
What you can expect when you are selected:
We are looking for someone who has:
Physical Demands:
Equal Employment Opportunity: At Online Labels Group, we don't just accept difference - we celebrate it, we support it, and we thrive on it for the benefit of our employees, our products, and our community. Online Labels Group is proud to be an equal opportunity workplace to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, or genetics.
Online Labels Group is a Drug-Free Workplace. This position is subject to a background check and drug testing.