Volga PartnersHiring

Regulatory Compliance Auditor Subject Matter Expert, AI Model Evaluation

  • USD 20 to 50 per hour
  • Remote, United States
  • Freelance
  • Senior
  • Posted 5 days ago
In one line

Freelance, task-based work for experienced pharmaceutical auditors who review AI-written compliance content and flag what is wrong. Remote in the US, paid by the hour.

About the role

Suits someone with a background in pharma auditing, quality systems and inspection readiness who wants occasional paid review work alongside their career. Assignments come as they are available and may be irregular.

At a glance

Pay
USD 20 to 50 per hour
Remote scope
Remote, United States
Seniority
Senior
Employment
Freelance
Skills
FDA requirements, GMP, ICH guidelines, Auditing, Quality systems, Inspection readiness
Posted
30 Oct 2026
Last checked
3 Nov 2026

What you will do

  • Check AI-written pharma answers for accuracy, completeness and consistency with industry rules
  • Read content on quality systems, manufacturing, validation, submissions and compliance work
  • Judge whether the conclusions drawn are backed by science and by regulators
  • Spot unsupported claims, technical mistakes, missing context and weak reasoning
  • Explain findings in writing and suggest corrections that are technically sound

What they look for

  • Hands-on experience in pharmaceutical auditing, regulatory compliance or quality systems
  • Familiarity with FDA requirements, GMP rules and ICH guidelines
  • Able to judge regulatory reasoning and audit scenarios without supervision
  • Clear written feedback that points to specific problems and fixes
  • Comfort working on an online platform and hitting project deadlines

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Questions about this job

Is this job fully remote, and from where?

Yes, it is listed as remote, aimed at candidates in the United States.

What does this job pay?

The posting states USD 20 to 50 per hour.

What experience is needed?

It is a senior role. The posting asks for: hands-on experience in pharmaceutical auditing, regulatory compliance or quality systems; familiarity with FDA requirements, GMP rules and ICH guidelines; able to judge regulatory reasoning and audit scenarios without supervision. Skills it names include FDA requirements, GMP, ICH guidelines, Auditing.

How do I apply with Keywordise AI?

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