Remote | United States | Project-Based Independent Contractor Compensation: $20-$50 USD/hour, based on specialty, experience, and project requirements Help Shape the Future of AI in Pharmaceutical What if your expertise in Pharmaceutical GMP compliance, validation programs, qualification activities, and regulator
About the role
Remote | United States | Project-Based Independent Contractor
Compensation: $20-$50 USD/hour, based on specialty, experience, and project requirements
Help Shape the Future of AI in Pharmaceutical
What if your expertise in Pharmaceutical GMP compliance, validation programs, qualification activities, and regulatory requirements could help artificial intelligence better understand pharmaceutical manufacturing controls, validation standards, and inspection readiness expectations?
At Volga Partners , we're connecting experienced pharmaceutical professionals with opportunities to contribute to the development and evaluation of advanced AI models.
We're seeking experienced Pharmaceutical GMP Compliance and Validation professionals who can apply their compliance expertise, technical knowledge, and industry experience to evaluate AI-generated pharmaceutical content.
This isn't a traditional validation or compliance position. You won't be executing validation protocols, leading qualification activities, managing compliance programs, or supporting regulatory inspections. Instead, you'll evaluate complex compliance and validation-related content, identify technical inaccuracies, assess regulatory reasoning, and provide structured feedback that improves AI model performance.
Your pharmaceutical expertise is what matters. AI experience is a plus, not a requirement.
Important Note: This is a freelance, task-based role designed for those seeking supplemental income. It’s essential to understand the nature of freelance work—tasks will be assigned as they become available, and work may be irregular or intermittent.
The Opportunity
As a GMP Compliance & Validation Subject Matter Expert (SME) , you'll serve as a subject matter evaluator, helping assess the quality, accuracy, completeness, and regulatory compliance of Pharmaceutical AI-generated content. …
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