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Part Time Fda Auditor Jobs (NOW HIRING)

Certified Group

Part-time Courier

Dallas, TX · On-site

$15.50 - $19.75/hr

EAS Consulting Group - A regulatory consulting firm offering expert guidance, training, and auditing support across FDA, USDA, and other regulated sectors, powered by a large network of independent ...

Eliquent Life Sciences, Inc

Consultant 1

Montrose, CA · On-site

Provide support during audits and inspections to ensure systems meet regulatory expectations (FDA ... Attractive salary and comprehensive benefits package for full-time and part-time employees ...

CookUnity

Food Safety Associate - Part Time

Chicago, IL · On-site

$18 - $20/hr

Ensure the facility is always ready for inspection by local regulator or third party auditor ... Experience working in a high compliance food processing facility (USDA, FDA) * Positive and ...

CookUnity

Food Safety Associate - Part Time

Chicago, IL · On-site

$18 - $20/hr

Ensure the facility is always ready for inspection by local regulator or third party auditor ... Experience working in a high compliance food processing facility (USDA, FDA) * Positive and ...

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Part Time Fda Auditor information

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$10

$19

$46

How much do part time fda auditor jobs pay per hour?

As of Jul 15, 2026, the average hourly pay for part time fda auditor in the United States is $19.21, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $19.23 per hour, depending on experience, location, and employer.
What are the most commonly searched types of Fda Auditor jobs? The most popular types of Fda Auditor jobs are:
Part Time Fda Auditor jobs near you
Senior Auditor, Vendor Audit (contract)

Senior Auditor, Vendor Audit (contract)

Premier Research

Remote

$70/hr

Part-time

Re-posted 23 days ago

Job description

Premier Research is looking for a Senior Auditor, Vendor Audit (contract) to join our Functional Services Provider (FSP) team.
You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.
  • We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires.
  • Your ideas influence the way we work, and your voice matters here.
  • As an essential part of our team, you help us deliver the medical innovation that patients are desperate for.

Join us and build your future here.
What you'll be doing:
  • Organizes and hosts Vendor audits to support global operations (including preparation of audit plans, audit checklists, audit reports and certificates)
  • Manages complex audit activities in accordance with the Premier Research Vendor audit schedule and ensures the approved vendor list remains up to date and that only approved vendors are listed as available for use at a study level.
  • Collaborates with operational teams to ensure any documented Vendor issues and/or gaps raised at a study level are reviewed on an ongoing basis and trended for potential systemic issues. Any systemic issues are formally documented, and corrective actions implemented at a global level (to include contracts etc. as appropriate).
  • Acts as Point of Contact (POC) for vendor audit activities.
  • Ensures compliance with established internal control procedures by examining records, reports, operating practices, and documentation.
  • Communicates audit findings by preparing a final report; discussing findings with auditees.

What we are searching for:
  • Bachelor's degree, or international equivalent from an accredited institution, in Health or Life Sciences, or equivalent experience
  • 5-8 years specialized GxP experience in auditing (i.e., vendor audits, GCP audits, GMP audits), or 8+ years relevant experience with 5+ years' experience conducting Vendor audits
  • Ability to interpret controlled documentation (i.e., protocols, validation documents, manufacturing records and data)
  • Demonstrated ability to independently review the majority of the following: databases, trial master files, investigator sites, statistical/clinical study reports, vendors, manufacturers,
    master batch records, device history files, laboratories, system validation documentation
  • Demonstrated knowledge of ICH Guidelines, FDA Code of Federal Regulations and other applicable regulatory authority laws and regulations
  • Preferred Location: East Coast
  • Please note this is a part-time 6 month 1099 contractor opportunity

Premier Research is dedicated to providing compensation that is fair and competitive with market standards. The starting hourly rate for this role is $70/hr USD. The actual hourly rate will be influenced based on a variety of factors such as the candidate's qualifications, skills, competencies, and proficiency for the role.
Premier Research is proud to be an equal opportunity employer that is compliant with all federal guidelines. All qualified applicants will receive equitable consideration without regard to race, color, religion, sexual orientation, gender identity, national origin, disability or veteran status

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