Pharmaceutical Subject Matter Expert – AI Model Evaluation

🔥 1 minute ago

🌐 United States, India, +3 more countries – Remote

🇺🇸 United States – Remote 🇮🇳 India – Remote 🇵🇰 Pakistan – Remote 🇯🇴 Jordan – Remote 🇪🇬 Egypt – Remote

💵 $20 - $40 / hour

⏳ Contract/Temporary

🟡 Mid-level

🟠 Senior

🤖 Artificial Intelligence

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 2%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Volga Partners

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 2020

🤖 Artificial Intelligence

🤝 B2B

🏢 Enterprise

Artificial Intelligence • B2B • Enterprise

Volga Partners is a technology services firm that specializes in Artificial Intelligence and Machine Learning solutions, data annotation and labeling, and development of customer service platforms powered by generative AI. The company also provides IT and software development services across web, app, full-stack, cybersecurity advisory, and e-commerce support, supported by a large multilingual crowd workforce and remote on-demand resources. Volga Partners focuses on partnering with enterprise clients to deliver scalable, cost-effective AI tooling, content moderation, linguistic services, and managed software projects.

📋 Description

• 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

• 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

• 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