QA/Analytical Development Subject Matter Expert – AI Model Evaluation

Job not on LinkedIn

🔥 18 minutes ago

🇺🇸 United States – Remote

💵 $25 - $50 / hour

⏳ Contract/Temporary

🟡 Mid-level

🟠 Senior

🔧 QA Engineer (Quality Assurance)

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This company has sponsored H1B visas in the past.

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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 scientific, technical, and regulatory accuracy, completeness, consistency, and compliance • Review information related to quality systems, manufacturing, validation, submissions, development, and compliance activities • 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, and recommend technically accurate corrections • Apply project-specific evaluation criteria, scoring guidelines, and quality standards • Complete independent evaluations on designated online platforms within project timelines

🎯 Requirements

• Minimum of 4 years of professional experience in Quality Control, Analytical Development, Analytical Chemistry, Pharmaceutical Testing, or related laboratory functions • Bachelor's degree or higher in Chemistry, Pharmaceutical Sciences, Pharmacy, Biochemistry, Biotechnology, Microbiology, Life Sciences, or a related discipline • Experience supporting pharmaceutical laboratory operations within regulated environments • Experience with analytical method development, validation, transfer, or routine testing activities • Familiarity with HPLC, UPLC, GC, LC-MS, UV, dissolution systems, or related technologies • Understanding of OOS, OOT, deviations, and root cause analysis • Knowledge of FDA regulations, GMP requirements, and relevant ICH guidelines • Experience reviewing scientific and manufacturing documentation • Ability to critically evaluate technical and regulatory information • Strong analytical, research, and problem-solving skills • Excellent written English communication skills • Ability to work independently and follow detailed review instructions • Comfortable working within a task-based freelance engagement model • AI model evaluation experience is beneficial but not required

🏖️ Benefits

• Remote work • Flexible, project-based assignments • Opportunity to contribute to advanced AI technologies • Experience contributing to AI evaluation initiatives • Supplemental-income freelance work

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