QA Lead Auditor
Dallas, TX · On-site
QA Lead Auditor - With Previous FDA Audit Experience. This position will be responsible for ... hourly rates on 1099 or C2C. • Reimbursement of all expenses while working on the project.
QA Lead Auditor
Dallas, TX · On-site
QA Lead Auditor - With Previous FDA Audit Experience. This position will be responsible for ... hourly rates on 1099 or C2C. • Reimbursement of all expenses while working on the project.
QA Lead Auditor
Dallas, TX · Hybrid
QA Lead Auditor - With Previous FDA Audit Experience. This position will be responsible for ... Exceptional hourly rates on 1099 or C2C. Reimbursement of all expenses while working on the project.
QA Lead Auditor
Dallas, TX · Hybrid
QA Lead Auditor - With Previous FDA Audit Experience. This position will be responsible for ... Exceptional hourly rates on 1099 or C2C. Reimbursement of all expenses while working on the project.
QA Lead Auditor
Dallas, TX · Hybrid
QA Lead Auditor - With Previous FDA Audit Experience. This position will be responsible for ... hourly rates on 1099 or C2C. • Reimbursement of all expenses while working on the project.
QA Lead Auditor
Dallas, TX · Hybrid
QA Lead Auditor - With Previous FDA Audit Experience. This position will be responsible for ... hourly rates on 1099 or C2C. • Reimbursement of all expenses while working on the project.
QA Lead Auditor
Dallas, TX · On-site
QA Lead Auditor - With Previous FDA Audit Experience. This position will be responsible for ... hourly rates on 1099 or C2C. · Reimbursement of all expenses while working on the project.
Quick apply
QA Lead Auditor
Dallas, TX · On-site
QA Lead Auditor - With Previous FDA Audit Experience. This position will be responsible for ... hourly rates on 1099 or C2C. · Reimbursement of all expenses while working on the project.
... the FDA and notified bodies. The position requires deep knowledge of quality systems within the ... Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from ...
... the FDA and notified bodies. The position requires deep knowledge of quality systems within the ... Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from ...
... the FDA and notified bodies. The position requires deep knowledge of quality systems within the ... Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from ...
... the FDA and notified bodies. The position requires deep knowledge of quality systems within the ... Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from ...
Senior QA Auditor
Santa Clarita, CA · On-site
... the FDA and notified bodies. The position requires deep knowledge of quality systems within the ... Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from ...
Senior QA Auditor
Santa Clarita, CA · On-site
... the FDA and notified bodies. The position requires deep knowledge of quality systems within the ... Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from ...
... the FDA and notified bodies. The position requires deep knowledge of quality systems within the ... Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from ...
... the FDA and notified bodies. The position requires deep knowledge of quality systems within the ... Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from ...
... the FDA and notified bodies. The position requires deep knowledge of quality systems within the ... Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from ...
... the FDA and notified bodies. The position requires deep knowledge of quality systems within the ... Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from ...
Senior QA Auditor
Santa Clarita, CA · On-site
... the FDA and notified bodies. The position requires deep knowledge of quality systems within the ... Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from ...
Senior QA Auditor
Santa Clarita, CA · On-site
... the FDA and notified bodies. The position requires deep knowledge of quality systems within the ... Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from ...
Quality Auditor
$22.28/hr
Ensure that device history records are completed according to FDA GMP requirements. Complete ... Hourly Incentive Eligible: No Sales Commission Eligible: No Disclaimer : We strive to provide ...
Quality Auditor
$22.28/hr
Ensure that device history records are completed according to FDA GMP requirements. Complete ... Hourly Incentive Eligible: No Sales Commission Eligible: No Disclaimer : We strive to provide ...
Quality Auditor
Noblesville, IN · On-site
$22.28/hr
Ensure that device history records are completed according to FDA GMP requirements. Complete ... Hourly Incentive Eligible: No Sales Commission Eligible: No Disclaimer : We strive to provide ...
Quality Auditor
Noblesville, IN · On-site
$22.28/hr
Ensure that device history records are completed according to FDA GMP requirements. Complete ... Hourly Incentive Eligible: No Sales Commission Eligible: No Disclaimer : We strive to provide ...
Quality Auditor
Noblesville, IN · On-site
$22.28/hr
Ensure that device history records are completed according to FDA GMP requirements. Complete ... Hourly Incentive Eligible: No Sales Commission Eligible: No Disclaimer : We strive to provide ...
Quality Auditor
Noblesville, IN · On-site
$22.28/hr
Ensure that device history records are completed according to FDA GMP requirements. Complete ... Hourly Incentive Eligible: No Sales Commission Eligible: No Disclaimer : We strive to provide ...
EDHR Reviewer - Quality (Molding)
Buffalo Grove, IL · On-site
$21.61 - $29.18/hr
ISO/FDA Auditing experience a plus. * Use of the following tools may be required: Office Skills ... Tuition Reimbursement Pay Range (Applicable to Illinois) $21.61 USD - $29.18 USD Hourly Job ...
EDHR Reviewer - Quality (Molding)
Buffalo Grove, IL · On-site
$21.61 - $29.18/hr
ISO/FDA Auditing experience a plus. * Use of the following tools may be required: Office Skills ... Tuition Reimbursement Pay Range (Applicable to Illinois) $21.61 USD - $29.18 USD Hourly Job ...
Biomaterials Production Operator - 2nd shift
Ontario, CA · On-site
$16.50 - $21/hr
... bodies, such as FDA auditors). The hourly pay range for this position is $16.50 - $21.00. The pay offered for this role may be influenced by factors such as job location, scope of role ...
Biomaterials Production Operator - 2nd shift
Ontario, CA · On-site
$16.50 - $21/hr
... bodies, such as FDA auditors). The hourly pay range for this position is $16.50 - $21.00. The pay offered for this role may be influenced by factors such as job location, scope of role ...
Ensure that device history records are completed according to FDA GMP requirements. Complete ... Hourly Incentive Eligible: No Sales Commission Eligible: No Disclaimer : We strive to provide ...
Ensure that device history records are completed according to FDA GMP requirements. Complete ... Hourly Incentive Eligible: No Sales Commission Eligible: No Disclaimer : We strive to provide ...
Quality Auditor-Cyclone
Noblesville, IN · On-site
$22.28/hr
Ensure that device history records are completed according to FDA GMP requirements. Complete ... Hourly Incentive Eligible: No Sales Commission Eligible: No Disclaimer : We strive to provide ...
Quality Auditor-Cyclone
Noblesville, IN · On-site
$22.28/hr
Ensure that device history records are completed according to FDA GMP requirements. Complete ... Hourly Incentive Eligible: No Sales Commission Eligible: No Disclaimer : We strive to provide ...
Quality Auditor-Cyclone
Noblesville, IN · On-site
$22.28/hr
Ensure that device history records are completed according to FDA GMP requirements. Complete ... Hourly Incentive Eligible: No Sales Commission Eligible: No Disclaimer : We strive to provide ...
Quality Auditor-Cyclone
Noblesville, IN · On-site
$22.28/hr
Ensure that device history records are completed according to FDA GMP requirements. Complete ... Hourly Incentive Eligible: No Sales Commission Eligible: No Disclaimer : We strive to provide ...
Hourly Fda Auditor information
See salary details
$33K - $41K
2% of jobs
$41K - $49.1K
17% of jobs
$53.3K is the 25th percentile. Wages below this are outliers.
$49.1K - $57.1K
12% of jobs
$57.1K - $65.2K
11% of jobs
The median wage is $69.5K / yr.
$65.2K - $73.2K
17% of jobs
$73.2K - $81.3K
7% of jobs
$81.3K - $89.3K
6% of jobs
$89.3K - $97.4K
3% of jobs
$97.5K is the 75th percentile. Wages above this are outliers.
$97.4K - $105.4K
17% of jobs
$105.4K - $113.5K
4% of jobs
$113.5K - $121.5K
4% of jobs
$33K
$76.3K
$121.5K
How much do hourly fda auditor jobs pay per year?
As of Jun 13, 2026, the average yearly pay for hourly fda auditor in the United States is $76,256.00, according to ZipRecruiter salary data. Most workers in this role earn between $53,500.00 and $98,500.00 per year, depending on experience, location, and employer.
What cities are hiring for Hourly Fda Auditor jobs? Cities with the most Hourly Fda Auditor job openings:
What are the most commonly searched types of Fda Auditor jobs? The most popular types of Fda Auditor jobs are:
What states have the most Hourly Fda Auditor jobs? States with the most job openings for Hourly Fda Auditor jobs include:
Contractor
Posted 20 days ago
Job description
QA Lead Auditor - With Previous FDA Audit Experience.
This position will be responsible for planning and conducting audit procedures, including identifying and defining audit issues, developing audit criteria, reviewing and analyzing evidence, documenting the status and operating procedures of the organization, and preparing audit reports. The Lead Auditor will be responsible for the assessment of the organization's quality system and compliance status in accordance with all relevant regulations and guidelines, such as 21CFR Parts 211, Parts 600s, Parts 3 &4, as well as Part 820. The lead auditor will independently perform quality audits of drug product manufacturing practices to ensure products, controls, procedures, and processes meet quality standards. The Lead Auditor will also prepare audit reports and communicate findings to stakeholders.
Responsibilities:
• Able to perform high-profile audits for manufacturing facilities and clinical trial sites.
• Lead a team of auditors, conduct manufacturing sites audits, and identify and follow up on any resolved audit findings identified during a Quality Assurance Audit.
• Adheres to all safety, environmental, and quality requirements, not limited to: Quality Management Systems (QMS), U.S. Food and Drug Administration (FDA) regulations, company policies and operating procedures, and other regulatory requirements.
• Schedules audit activities with the internal sites and provide audit agenda.
• Writes audit reports of findings, recommendations, and management corrective action plans.
• Assure that issues from sponsor audits are promptly communicated to the appropriate team
• Tracks audit responses and auditees' remediation CAPAs until completion and closeout.
• Independently performs evaluations of quality systems and practices to identify potential problems
• Stays up to date on current FDA and Health Canada manufacturing trends
Education & Experience & Knowledge & Skills:
• Previous work experience with FDA or Health Canada Agencies is a requirement.
• Minimum of a BS degree in science with a minimum of 5+ years of experience in performing and discussing audits.
• Thorough knowledge of current standard practice and regulations
• Ability to review technical documents
This unique opportunity provides:
• Exceptional hourly rates on 1099 or C2C.
• Reimbursement of all expenses while working on the project.
Requirements
Education & Experience & Knowledge & Skills:
• Previous work experience with FDA regulations and GMP requirements is required.
• Minimum of a BS degree in science with a minimum of 5+ years of experience in performing and discussing audits.
• Thorough knowledge of current standard practice and regulations
• Ability to review technical documents
Location:
• Hybrid work style with requirements to travel overseas to perform onsite audits
Benefits
This unique opportunity provides:
• Exceptional hourly rates on 1099 or C2C.
• Reimbursement of all expenses, while working on the project.
This position will be responsible for planning and conducting audit procedures, including identifying and defining audit issues, developing audit criteria, reviewing and analyzing evidence, documenting the status and operating procedures of the organization, and preparing audit reports. The Lead Auditor will be responsible for the assessment of the organization's quality system and compliance status in accordance with all relevant regulations and guidelines, such as 21CFR Parts 211, Parts 600s, Parts 3 &4, as well as Part 820. The lead auditor will independently perform quality audits of drug product manufacturing practices to ensure products, controls, procedures, and processes meet quality standards. The Lead Auditor will also prepare audit reports and communicate findings to stakeholders.
Responsibilities:
• Able to perform high-profile audits for manufacturing facilities and clinical trial sites.
• Lead a team of auditors, conduct manufacturing sites audits, and identify and follow up on any resolved audit findings identified during a Quality Assurance Audit.
• Adheres to all safety, environmental, and quality requirements, not limited to: Quality Management Systems (QMS), U.S. Food and Drug Administration (FDA) regulations, company policies and operating procedures, and other regulatory requirements.
• Schedules audit activities with the internal sites and provide audit agenda.
• Writes audit reports of findings, recommendations, and management corrective action plans.
• Assure that issues from sponsor audits are promptly communicated to the appropriate team
• Tracks audit responses and auditees' remediation CAPAs until completion and closeout.
• Independently performs evaluations of quality systems and practices to identify potential problems
• Stays up to date on current FDA and Health Canada manufacturing trends
Education & Experience & Knowledge & Skills:
• Previous work experience with FDA or Health Canada Agencies is a requirement.
• Minimum of a BS degree in science with a minimum of 5+ years of experience in performing and discussing audits.
• Thorough knowledge of current standard practice and regulations
• Ability to review technical documents
This unique opportunity provides:
• Exceptional hourly rates on 1099 or C2C.
• Reimbursement of all expenses while working on the project.
Requirements
Education & Experience & Knowledge & Skills:
• Previous work experience with FDA regulations and GMP requirements is required.
• Minimum of a BS degree in science with a minimum of 5+ years of experience in performing and discussing audits.
• Thorough knowledge of current standard practice and regulations
• Ability to review technical documents
Location:
• Hybrid work style with requirements to travel overseas to perform onsite audits
Benefits
This unique opportunity provides:
• Exceptional hourly rates on 1099 or C2C.
• Reimbursement of all expenses, while working on the project.
About Synergy BIS
Sourced by ZipRecruiter
Company size
501 - 1,000 Employees
Headquarters location
Reston, VA, US
Year founded
2005