Pharmaceutical Manufacturing Science & Technology Subject Matter Expert - AI

Remote | United States | Project-Based Independent Contractor

Compensation: $20-$50 USD/hour, based on specialty, experience, and project requirements

What if your expertise in pharmaceutical manufacturing, process optimization, technology transfer, and Manufacturing Science & Technology (MSAT) could help artificial intelligence better understand pharmaceutical production processes, operational excellence, and manufacturing best practices?

At Volga Partners
, we’re connecting experienced pharmaceutical professionals with opportunities to contribute to the development and evaluation of advanced AI models.

We’re seeking experienced Pharmaceutical Manufacturing and MSAT professionals who can apply their manufacturing expertise, technical judgment, and industry knowledge to evaluate AI-generated pharmaceutical content.

Your pharmaceutical expertise is what matters. AI experience is a plus, not a requirement.

Important Note:

This is a freelance, task-based role designed for those seeking supplemental income. It’s essential to understand the nature of freelance work—tasks will be assigned as they become available, and work may be irregular or intermittent.

As a Pharmaceutical Manufacturing / Manufacturing Science & Technology (MSAT) Subject Matter Expert (SME), you’ll serve as a subject matter evaluator, helping assess the quality, accuracy, completeness, and scientific validity of Pharmaceutical AI-generated content.

You’ll analyze manufacturing, process engineering, technology transfer, operational excellence, facility operations, and quality-related scenarios, identify errors or unsupported conclusions, and provide expert feedback grounded in pharmaceutical manufacturing principles, regulatory expectations, and industry best practices.

Your contributions will help improve how AI systems understand and respond to complex pharmaceutical and biotechnology challenges.

• Evaluate AI-generated pharmaceutical content: Assess scientific, technical, and regulatory responses for accuracy, completeness, consistency, and compliance with industry standards.
• Review scientific and regulatory information: Examine content related to quality systems, manufacturing, validation, submissions, development, and compliance activities.
• Analyze technical reasoning: Determine whether AI-generated conclusions are supported by relevant scientific principles, regulatory expectations, and industry best practices.
• Identify errors and inconsistencies: Recognize unsupported claims, technical inaccuracies, missing context, and flawed reasoning.
• Validate information: Reference relevant FDA requirements, GMP regulations, ICH guidelines, and accepted pharmaceutical industry practices.
• Provide expert feedback: Clearly explain findings, identify opportunities for improvement, and recommend technically accurate corrections.
• Support AI quality improvement: Apply project-specific evaluation criteria, scoring guidelines, and quality standards.
• Complete independent evaluations: Use designated online platforms to complete assignments accurately and within established project timelines.

Apply Your Industry Expertise in a New Way
Use the knowledge you’ve developed throughout your pharmaceutical or biotechnology career to contribute to advanced AI technologies.

Help Improve Scientific Accuracy
Your evaluations will help strengthen the quality and reliability of AI-generated pharmaceutical and regulatory information.

Work Remotely
Participate in project-based assignments from an eligible location, with flexibility based on project needs and availability.

Explore the Future of Pharmaceutical Technology
Gain experience contributing to AI evaluation initiatives while…