Pharma MSAT SME for AI Content Evaluation (Remote)

Volga Partners; United States; Remote; USD 28,000 - 69,000; Part time

Job summary

Volga Partners seeks experienced Pharmaceutical Manufacturing and MSAT professionals to act as SME evaluators for AI-generated pharmaceutical content. You will assess accuracy, regulatory alignment, and technical reasoning across quality systems, manufacturing, submissions, and process validation in a remote, project-based setting.

This freelance role offers flexible assignments, varying hours, and the chance to shape how AI understands pharmaceutical manufacturing.

Qualifications

• Minimum 4 years in Pharmaceutical Manufacturing/MSAT or related operations.
• Experience with GMP environments and regulatory understanding.
• Strong analytical, research, and problem-solving skills.
• Excellent written English communication.

Responsibilities

• Evaluate AI-generated pharmaceutical content for accuracy, completeness, and regulatory compliance.
• Review scientific and regulatory information related to quality systems, manufacturing, validation, submissions, and compliance.
• Analyze technical reasoning to ensure support by scientific principles and regulatory expectations.
• Identify errors, inconsistencies, missing context, and flawed reasoning.
• Validate information referencing FDA requirements, GMP regulations, ICH guidelines, and industry practices.
• Provide expert feedback with clear explanations and corrective recommendations.
• Support AI quality improvement using project-specific evaluation criteria and timelines.
• Complete independent evaluations on designated online platforms within deadlines.

Skills

Pharmaceutical MSAT experience

Regulatory understanding

Excellent written English

Education

Bachelor's degree or higher in Pharmaceutical Sciences / Pharmacy / Chemical Engineering / Biotechnology / Chemistry / Biochemistry / Biomedical Engineering / Life Sciences

Job description

Volga Partners seeks experienced Pharmaceutical Manufacturing and MSAT professionals to act as SME evaluators for AI-generated pharmaceutical content. You will assess accuracy, regulatory alignment, and technical reasoning across quality systems, manufacturing, submissions, and process validation in a remote, project-based setting.

This freelance role offers flexible assignments, varying hours, and the chance to shape how AI understands pharmaceutical manufacturing.