Pharmaceutical Manufacturing Science & Technology Subject Matter Expert – AI

Job not on LinkedIn

🔥 1 minute ago

🇺🇸 United States – Remote

💵 $25 - $50 / hour

⏳ Contract/Temporary

🟡 Mid-level

🟠 Senior

🤖 Artificial Intelligence

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 2%

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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 using designated online platforms within project timelines

🎯 Requirements

• Minimum of 4 years of professional experience in Pharmaceutical Manufacturing, Manufacturing Science & Technology (MSAT), Technical Operations, Process Engineering, Production Support, or related pharmaceutical functions • Bachelor's degree or higher in Pharmaceutical Sciences, Pharmacy, Chemical Engineering, Biotechnology, Chemistry, Biochemistry, Biomedical Engineering, Life Sciences, or a related discipline • Experience supporting pharmaceutical manufacturing operations in GMP-regulated environments • Experience with process monitoring, process optimization, manufacturing investigations, or technical operations support • Understanding of pharmaceutical production processes and manufacturing controls • Knowledge of FDA regulations, GMP requirements, and relevant ICH guidelines • Experience reviewing manufacturing documentation, batch records, process performance data, or technical reports • 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 • Preferred: PharmD, MS, MBA, PhD, or other advanced scientific credentials • Preferred: Experience supporting technology transfer from development to commercial manufacturing • Preferred: Experience troubleshooting manufacturing deviations and process issues • Preferred: Experience with process characterization, process validation, and continued process verification • Preferred: Experience supporting sterile, biologic, vaccine, or oral solid dosage manufacturing operations • Preferred: Knowledge of Lean Manufacturing, Six Sigma, Operational Excellence, or Continuous Improvement methodologies • Preferred: Experience collaborating with Quality Assurance, Validation, Regulatory Affairs, Engineering, and Supply Chain teams • Preferred: Experience interpreting process performance metrics and manufacturing trends • Preferred: Experience with technical writing, investigation reports, or manufacturing documentation review • Preferred: Familiarity with AI evaluation, data annotation, or quality review activities

🏖️ Benefits

• Remote work arrangement • Flexible, assignment-based schedule • Opportunity to contribute to advanced AI technologies • Supplemental-income freelance engagement • Experience contributing to AI evaluation initiatives

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