Volga PartnersHiring

Pharmaceutical CMC Regulatory Affairs Subject Matter Expert, AI Model Evaluation

  • USD 20 to 50 per hour
  • Remote, United States
  • Freelance
  • Senior
  • Posted 7 days ago
Apply with Keywordise AI

or apply from Claude / ChatGPT / Muse

In one line

Freelance, task-based work reviewing AI-generated pharmaceutical regulatory content for accuracy and compliance; remote in the United States.

About the role

The work is judging model output against real regulatory and manufacturing knowledge, flagging errors and unsupported claims, and writing structured feedback that improves the model.

At a glance

Pay
USD 20 to 50 per hour
Remote scope
Remote, United States
Seniority
Senior
Employment
Freelance
Skills
CMC regulatory affairs, GMP, ICH guidelines, FDA requirements, Quality systems, Validation
Posted
28 Oct 2026
Last checked
3 Nov 2026

What you will do

  • Assess AI-written pharmaceutical and regulatory answers for accuracy, completeness and consistency
  • Check content on quality systems, manufacturing, validation, submissions and compliance
  • Judge whether conclusions follow from scientific principles and regulatory expectations
  • Point out unsupported claims, technical errors, missing context and weak reasoning
  • Cite FDA requirements, GMP rules, ICH guidelines and accepted industry practice when validating content
  • Explain findings clearly and suggest technically correct fixes

What they look for

  • Experience in CMC regulatory affairs in the pharmaceutical or biotech industry
  • Ability to read scientific and regulatory material closely and spot technical errors
  • Clear written feedback that explains why something is wrong
  • Familiarity with AI work is a plus, not a requirement

Benefits

  • Pay of $20 to $50 USD per hour, set by specialty, experience and project needs
  • Remote work done as an independent contractor

How Keywordise applies for you

  1. 1Upload your CVAdd your CV once. It takes about a minute.
  2. 2Tailored to this jobKeywordise writes a CV and a cover letter for this job from your real experience.
  3. 3The form fills itselfName, email, experience and screening questions, field by field.
  4. 4Application sentYou get a receipt and follow it in your dashboard.

Apply with Keywordise AI7-day free trial, no card.

Apply from your AI assistant

Connect Keywordise to your assistant once, then send it the prompt. It applies for you.

ClaudeConnectorChatGPTConnectorMuseby Meta

Claude

  1. In Claude, open Settings, then Connectors, and choose Add custom connector.
  2. Name it Keywordise and paste the connector URL.
  3. Click Connect, log in to Keywordise and approve. Then send the prompt in a new chat.
Connector URL
https://keywordise.com/mcp

Disconnect any time in your Keywordise settings.

ChatGPT

  1. In ChatGPT, open Settings, then Connectors. On plans that need it, turn on developer mode first.
  2. Add a new connector with the connector URL and choose OAuth. Leave the client ID and secret empty.
  3. Log in to Keywordise and approve. Then send the prompt in a new chat.
Connector URL
https://keywordise.com/mcp

Disconnect any time in your Keywordise settings.

Muse

  1. Open Muse (muse.ai or the app) and send it the message below.
  2. If Muse asks how to sign in, answer OAuth. Open the sign-in link it sends, log in to Keywordise and approve.
  3. Send the prompt. Muse asks before it sends anything.
Message for Muse
Add a custom connector called Keywordise. It is a remote MCP server at https://keywordise.com/mcp and uses OAuth. Give me the sign-in link.

Muse is available in the US only for now.

Prompt
Apply to Keywordise job uxvdafflfp
How to connect

Questions about this job

Is this job fully remote, and from where?

Yes. The posting lists Pharmaceutical CMC Regulatory Affairs 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: experience in CMC regulatory affairs in the pharmaceutical or biotech industry; ability to read scientific and regulatory material closely and spot technical errors; clear written feedback that explains why something is wrong. Skills it names include CMC regulatory affairs, GMP, ICH guidelines, FDA requirements.

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.

More remote science and research jobs

All remote science and research jobs
Volga PartnersRemote, United States
Apply with Keywordise AI