Volga PartnersHiring

QA/Analytical Development 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 pharma QC and analytical development specialists who review AI-generated scientific content and flag errors. Remote in the US, paid hourly.

About the role

Evaluating AI output on quality systems, manufacturing, validation and compliance topics, and scoring it against regulatory expectations. Work arrives as tasks are available, so volume varies.

At a glance

Pay
USD 20 to 50 per hour
Remote scope
Remote, United States
Seniority
Senior
Employment
Freelance
Skills
Quality control, Analytical development, GMP, ICH guidelines, FDA requirements, Method development
Posted
30 Oct 2026
Last checked
2 Nov 2026

What you will do

  • Check AI-generated pharmaceutical answers for accuracy, completeness and regulatory fit
  • Review content on quality systems, manufacturing, validation, submissions and compliance
  • Judge whether conclusions follow from accepted scientific and regulatory principles
  • Point out unsupported claims, missing context and flawed reasoning
  • Cite FDA requirements, GMP rules and ICH guidelines when validating information
  • Write clear feedback with recommended corrections and use the project scoring guidelines

What they look for

  • Hands-on background in pharmaceutical quality control or analytical development
  • Knowledge of method development, laboratory investigations and regulatory expectations
  • Ability to explain technical findings clearly in writing

Nice to have

  • Experience with AI or model evaluation work

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Questions about this job

Is this a remote job, and where can I work from?

Yes. The posting lists QA/Analytical Development 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 background in pharmaceutical quality control or analytical development; knowledge of method development, laboratory investigations and regulatory expectations; ability to explain technical findings clearly in writing. Skills it names include Quality control, Analytical development, GMP, 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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