Pharmaceutical Subject Matter Expert – AI Model Evaluation

Volga Partners

. Evaluate AI-generated pharmaceutical content for accuracy, completeness, consistency, and compliance with industry standards .

Posted 10/27/2026contractRemote • United States, India, Pakistan, Jordan, EgyptMid-LevelSenior💰 $20 - $40 per hourWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in evaluating AI-generated pharmaceutical content for accuracy and compliance with FDA requirements and GMP regulations. Proficient in analyzing scientific and regulatory information while providing expert feedback and recommendations for improvements.

Highest-signal resume keywords

Pharmaceutical Quality AssuranceRegulatory Compliance AuditingGMP Compliance / ValidationTechnical WritingFDA Requirements

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Scientific EvaluationRegulatory Submission PreparationQuality ControlAnalytical DevelopmentProblem-SolvingResearch SkillsAI Model EvaluationData AnnotationRubric DevelopmentCompliance Assessments

Soft Skills

Excellent Written CommunicationAnalytical AbilitiesConfidence in Reviewing Complex InformationAbility to Work IndependentlyAttention to Detail

Tools & Technologies

Digital PlatformsWeb-Based ApplicationsOnline Research Tools

Certifications & Qualifications

PharmDPhDAdvanced Scientific Credentials

Industry Keywords

Pharmaceutical IndustryBiotechnology IndustryFDA RegulationsICH GuidelinesQuality SystemsTechnical DevelopmentRegulatory AffairsManufacturing ComplianceScientific Content AssessmentTask-Based Freelance Engagement

About the role

Key responsibilities & impact

Evaluate AI-generated pharmaceutical content for accuracy, completeness, consistency, and compliance with industry standards
Review scientific and regulatory 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
Validate information against FDA requirements, GMP regulations, ICH guidelines, and accepted pharmaceutical industry practices
Provide expert feedback, explain findings, identify improvements, and recommend technically accurate corrections
Apply project-specific evaluation criteria, scoring guidelines, and quality standards
Complete independent evaluations using designated online platforms within project timelines

Requirements

What you’ll need

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: CMC Regulatory Affairs; Pharmaceutical Quality Assurance; CMC Science / Technical Development; Regulatory CMC Submission Writing; Quality Control / Analytical Development; GMP Compliance / Validation; Regulatory Compliance Auditing; or Pharmaceutical Manufacturing / MSAT
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
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 preferred
Experience performing quality reviews, regulatory audits, or scientific content evaluations preferred
Experience with technical writing, structured reviews, or compliance assessments preferred
Familiarity with AI model evaluation, prompt review, rubric development, or data annotation preferred
Previous involvement in scientific, regulatory, quality, or technical content assessment activities preferred

Benefits

Comp & perks

Remote work from an eligible location
Flexible, variable, assignment-based schedule
Project-based assignments
Opportunity to contribute to advanced AI technologies
Opportunity to improve scientific accuracy of AI-generated pharmaceutical information
Experience contributing to AI evaluation initiatives
Supplemental-income freelance engagement