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$33K

$76.3K

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How much do remote fda auditor jobs pay per year?

As of Jun 9, 2026, the average yearly pay for remote 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 are some common challenges faced by Remote FDA Auditors, and how can they be managed effectively?

Remote FDA Auditors often encounter challenges such as limited access to physical documents, time zone differences with global clients, and ensuring secure communication. To manage these effectively, auditors should familiarize themselves with digital audit tools, establish clear communication protocols with clients, and stay updated on remote auditing best practices. Proactive planning and strong organizational skills are essential for success in this role.

What is the difference between Remote Fda Auditor vs Remote Quality Assurance Specialist?

AspectRemote Fda AuditorRemote Quality Assurance Specialist
CertificationsFDA auditor certification, GxP, GMP, GLPISO, Six Sigma, GMP, GCP
Work EnvironmentRegulatory agencies, pharmaceutical, biotech companiesManufacturing, clinical trials, healthcare companies
Industry UsagePrimarily in pharma, biotech, medical devicesBroader across healthcare, manufacturing, biotech

The Remote Fda Auditor focuses on ensuring compliance with FDA regulations through audits of facilities and processes, mainly in pharma and biotech industries. The Remote Quality Assurance Specialist oversees quality systems, policies, and procedures across various healthcare sectors. While both roles require knowledge of GMP and regulatory standards, the Fda Auditor emphasizes compliance verification, whereas the QA Specialist concentrates on maintaining quality standards throughout the organization.

What are Remote FDA Auditors?

Remote FDA Auditors are professionals who conduct audits and inspections of facilities, processes, and documentation to ensure compliance with the U.S. Food and Drug Administration (FDA) regulations, but they do so virtually rather than on site. Using digital tools and secure platforms, they review records, interview staff, and assess procedures from a remote location. This approach increases flexibility and efficiency while maintaining the integrity of compliance checks. Remote FDA Auditors are especially vital for organizations in the pharmaceutical, biotech, food, and medical device industries that must adhere to FDA standards.

What are the key skills and qualifications needed to thrive as a Remote FDA Auditor, and why are they important?

To thrive as a Remote FDA Auditor, you need a deep understanding of FDA regulations, auditing procedures, and quality management systems, typically supported by a degree in life sciences or a related field. Familiarity with electronic audit management tools, documentation systems, and relevant certifications such as Certified Quality Auditor (CQA) are highly valuable. Strong attention to detail, analytical thinking, and effective virtual communication are crucial soft skills for this role. These competencies ensure accurate compliance assessments, clear reporting, and effective collaboration while working remotely.
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What cities are hiring for Remote Fda Auditor jobs? Cities with the most Remote Fda Auditor job openings:
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Remote Fda Auditor jobs near you
Infographic showing various Remote Fda Auditor job openings in the United States as of May 2026, with employment types broken down into 4% Internship, 76% Full Time, 9% Part Time, 7% Temporary, 2% Contract, and 2% Nights. Highlights an 87% Physical, 6% Hybrid, and 7% Remote job distribution, with an average salary of $76,256 per year, or $36.7 per hour.
Pharmaceutical Quality GVP Auditors Freelance/Independent (Consulting)

Pharmaceutical Quality GVP Auditors Freelance/Independent (Consulting)

Advarra

Remote

Part-time

Posted yesterday

Job description

If you're not already part of our Network, please register using the Expert Enrollment Form. https://advarra.my.site.com/experts/s/ Registration is required to be considered.
If you are in our network DO NOT fill out this form or click on the link.
Location
This role is open to candidates based in North America.
Company Information
At Advarra, we seek to foster an inclusive and collaborative environment where everyone is treated with respect and diverse perspectives are embraced. Treating one another, our clients, and clinical trial participants with empathy and care are key tenets of our culture at Advarra; we are committed to creating a workplace where each person is not only valued but empowered to thrive and make a meaningful impact.
Company Culture
Our people--both employees and consultants-are the heart of Advarra. They are the key to our success and the driving force behind our mission and vision. Our values (Patient-Centric, Ethical, Quality Focused, Collaborative) guide our actions and decisions. Knowing the impact of our work on trial participants and patients, we act with urgency and purpose to advance clinical research so that people can live happier, healthier lives.
Job Overview Summary
Advarra is seeking Good Pharmacovigilance Practice (GVP) Auditors to join our consultant network for North America -based projects. Auditors support compliance reviews across GVP clinical sites and vendors.
Job Duties & Responsibilities
  • Conduct Good Pharmacovigilance Practice (GVP) audits (planning, agenda, physical or remote audit, and report writing)
  • Evaluate investigator sites, CROs, and vendor compliance or qualification.
  • Prepare comprehensive audit reports detailing findings and root-causes.
  • Provide written audit reports in English.
  • If required will provide corrective actions support and present findings to QA leadership and stakeholders
  • Work collaboratively with clients to ensure quality standards.

Basic Qualifications
  • Minimum 10+ years of Clinical Quality Assurance and/or Good Pharmacovigilance Practice (GVP) experience.
  • Minimum 5+ years of Good Clinical Practices auditing experience.
  • Demonstrated experience with regulatory agency expectations (e.g., FDA, EMA) and audit readiness activities.
  • Demonstrated experience in developing and implementing quality assurance plans, audit programs, and corrective action plans.
  • Fluent English communication, verbal and written
  • Bachelor's degree

Preferred Qualifications
  • Strong interpersonal and client interaction skills.
  • Excellent analytical, problem-solving, communication, and report-writing skills.
  • Ability to work collaboratively across departments and interact with internal and external stakeholders.

Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
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About Advarra

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

201 - 500 Employees

Headquarters location

Columbia, MD, US

Year founded

1983

Social media

Twitter

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