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Regulatory Compliance Auditor Subject Matter Expert -AI Model Evaluation
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Job Description
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 auditing, regulatory compliance, quality systems, and inspection readiness could help artificial intelligence better understand compliance risks, regulatory expectations, and audit best practices?
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 Regulatory Compliance Auditors who can apply their auditing expertise, compliance knowledge, and industry experience to evaluate AI-generated pharmaceutical content. This isn't a traditional auditing position.
You won't be conducting supplier audits, preparing organizations for regulatory inspections, or managing compliance programs.
Instead, you'll evaluate complex compliance and audit-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 Regulatory Compliance Auditor 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.
You'll analyze auditing, quality, manufacturing, compliance, supplier oversight, and inspection-readiness scenarios, identify errors or unsupported conclusions, and provide expert feedback grounded in regulatory requirements, audit principles, and p
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