Remote Pharma SME for AI Content Evaluation

Volga Partners; United States; Remote; USD 28,000 - 55,000; Full time

Job summary

Volga Partners is seeking Pharmaceutical SMEs to evaluate AI-generated pharmaceutical and regulatory content from the US industry. You will assess scientific and regulatory information, identify errors, and provide structured feedback grounded in FDA requirements, GMPs, and ICH guidelines.

Remote, project-based freelance engagement with flexible schedules. Applicants should have pharmaceutical or biotech expertise and demonstrate independent, high-quality evaluations for AI model improvement.

Qualifications

• 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 pharmaceutical specialty listed above.
• 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.

Responsibilities

• Evaluate AI-generated pharmaceutical content: Assess scientific, technical, and regulatory responses for accuracy, completeness, consistency, and compliance with industry standards.
• Review scientific and regulatory information: Examine content related to quality systems, manufacturing, validation, submissions, development, and compliance activities.
• Analyze technical reasoning: Determine whether AI-generated conclusions are supported by relevant scientific principles, regulatory expectations, and industry best practices.
• Identify errors and inconsistencies: Recognize unsupported claims, technical inaccuracies, missing context, and flawed reasoning.
• Validate information: Reference relevant FDA requirements, GMP regulations, ICH guidelines, and accepted pharmaceutical industry practices.
• Provide expert feedback: Clearly explain findings, identify opportunities for improvement, and recommend technically accurate corrections.
• Support AI quality improvement: Apply project-specific evaluation criteria, scoring guidelines, and quality standards.
• Complete independent evaluations: Use designated online platforms to complete assignments accurately and within established project timelines.

Skills

Regulatory knowledge

Quality systems

Analytical thinking

Technical evaluation

Independent work

Education

Bachelor's degree or higher in Pharmacy, Pharmaceutical Sciences, Chemistry, Biotechnology, Engineering, Regulatory Affairs, or a related discipline

Job description

Volga Partners is seeking Pharmaceutical SMEs to evaluate AI-generated pharmaceutical and regulatory content from the US industry. You will assess scientific and regulatory information, identify errors, and provide structured feedback grounded in FDA requirements, GMPs, and ICH guidelines.

Remote, project-based freelance engagement with flexible schedules. Applicants should have pharmaceutical or biotech expertise and demonstrate independent, high-quality evaluations for AI model improvement.