Volga PartnersHiring

GMP Compliance & Validation Subject Matter Expert, AI Model Evaluation

  • USD 20 to 50 per hour
  • Remote, United States
  • Freelance
  • Senior
  • Posted 6 days ago
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In one line

Freelance, task-based work reviewing AI-written pharmaceutical compliance content and correcting it, done remotely from anywhere in the United States.

About the role

Tasks arrive as projects open, so the volume is irregular and suits people who want extra income. You judge AI answers on validation, quality systems and inspection readiness rather than running compliance programs.

At a glance

Pay
USD 20 to 50 per hour
Remote scope
Remote, United States
Seniority
Senior
Employment
Freelance
Skills
GMP, Validation, FDA Regulations, ICH Guidelines, Quality Systems, Inspection Readiness
Posted
29 Oct 2026
Last checked
3 Nov 2026

What you will do

  • Assess AI-generated pharmaceutical answers for accuracy, completeness and regulatory fit
  • Check content on quality systems, manufacturing, validation, submissions and development
  • Judge whether conclusions rest on sound science and accepted regulatory expectations
  • Flag unsupported claims, technical errors, missing context and weak reasoning
  • Write clear feedback with corrections, using FDA rules, GMP and ICH guidelines as reference

What they look for

  • Hands-on experience with pharmaceutical GMP compliance, validation and qualification work
  • Familiarity with regulatory requirements and inspection readiness in regulated plants
  • Ability to explain technical findings clearly in written feedback

Nice to have

  • Prior experience with AI evaluation is helpful but not required

How Keywordise applies for you

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Claude

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Connector URL
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Muse

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Message for Muse
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Muse is available in the US only for now.

Prompt
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How to connect

Questions about this job

Is this job fully remote, and from where?

Yes. The posting lists GMP Compliance & Validation Subject Matter Expert, AI Model Evaluation as a remote role for 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 with pharmaceutical GMP compliance, validation and qualification work; familiarity with regulatory requirements and inspection readiness in regulated plants; ability to explain technical findings clearly in written feedback. Skills it names include GMP, Validation, FDA Regulations, ICH Guidelines.

How do I apply with Keywordise AI?

Select Apply with Keywordise AI, sign up and upload your CV. Keywordise writes a CV and a cover letter for this job from your real experience and applies for you. The 7-day free trial needs no card.

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