Pharmaceutical experts evaluating AI-generated regulatory, scientific, and manufacturing content for Volga Partners. Providing structured feedback to improve healthcare AI models.
Responsibilities
Evaluate AI-generated pharmaceutical content for scientific, technical, and regulatory accuracy, completeness, consistency, and compliance
Review information related to quality systems, manufacturing, validation, submissions, development, and compliance
Analyze whether AI-generated conclusions are supported by scientific principles, regulatory expectations, and industry best practices
Identify unsupported claims, technical inaccuracies, missing context, and flawed reasoning
Reference FDA requirements, GMP regulations, ICH guidelines, and accepted pharmaceutical industry practices
Provide expert feedback, explain findings, identify improvements, and recommend accurate corrections
Apply project-specific evaluation criteria, scoring guidelines, and quality standards
Complete independent evaluations using designated online platforms within project timelines
Requirements
Minimum of four years of relevant professional experience in the regulated US based pharmaceutical or biotechnology industry
Bachelor's degree or higher in Pharmacy, Pharmaceutical Sciences, Chemistry, Biotechnology, Engineering, Regulatory Affairs, or a related discipline
Strong expertise in at least one listed pharmaceutical specialty
Working knowledge of FDA requirements, GMP regulations, and relevant ICH guidelines, including applicable portions of ICH Q7-Q12
Ability to critically evaluate scientific, technical, and regulatory information
Strong analytical, research, and problem-solving abilities
Excellent written English communication skills
Confidence reviewing complex information and explaining technical conclusions
Comfort using digital platforms, web-based applications, and online research tools
Ability to work independently, follow detailed instructions, and meet established quality standards
Must understand and be comfortable with a task-based freelance engagement model
Preferred: PharmD, PhD, or advanced scientific credentials
Preferred: Experience preparing or reviewing regulatory submissions (IND, NDA, BLA, ANDA, MAA, or equivalent)
Preferred: Experience with FDA-regulated manufacturing, quality, compliance, validation, or development environments
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