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 GMP compliance, validation programs, qualification activities, and regulatory requirements could help artificial intelligence better understand pharmaceutical manufacturing controls, validation standards, and inspection readiness expectations?
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 GMP Compliance and Validation professionals who can apply their compliance expertise, technical knowledge, and industry experience to evaluate AI-generated pharmaceutical content.
This isn't a traditional validation or compliance position. You won't be executing validation protocols, leading qualification activities, managing compliance programs, or supporting regulatory inspections. Instead, you'll evaluate complex compliance and validation-related content, identify technical inaccuracies, assess regulatory reasoning, and provide structured feedback that improves AI model performance.
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 GMP Compliance & Validation Subject Matter Expert (SME), you'll serve as a subject matter evaluator, helping assess the quality, accuracy, completeness, and regulatory compliance of Pharmaceutical AI-generated content.
You'll analyze validation, quality, manufacturing, engineering, compliance, and inspection-readiness scenarios, identify errors or unsupported conclusions, and provide expert feedback grounded in GMP regulations, validation principles, and pharmaceutical industry best practices.
Your contributions will help improve how AI systems understand and respond to complex compliance, qualification, and validation challenges across regulated pharmaceutical environments.
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 applying your existing scientific and regulatory expertise.
No AI Background Required
We're looking for professionals who can recognize accurate scientific reasoning, identify errors, and communicate expert assessments with clarity.
Volga Partners offers project-based hourly compensation based on specialization, relevant experience, professional qualifications, geographic location, and assignment requirements.
GMP Compliance & Validation Subject Matter Expert: $25-$50 USD/hour
Compensation may vary based on experience level, area of expertise, and task complexity.
Specific assignments, schedules, workloads, and project dates will be communicated as they are confirmed. Hours and future assignments are not guaranteed.
If you're an experienced pharmaceutical or biotechnology professional who enjoys analyzing complex scientific information, applying regulatory and technical expertise, and contributing to innovative technology, we'd love to hear from you.
Join Volga Partners and help shape the next generation of pharmaceutical AI.
Apply today to be considered for upcoming project opportunities.
Requirements
We're seeking experienced GMP Compliance and Validation professionals who bring practical industry expertise and are comfortable reviewing technical information, exercising independent judgment, and clearly explaining their conclusions.
We encourage applications from professionals with backgrounds such as:
Experience with AI model evaluation, large language models (LLMs), research, or structured quality assessments is beneficial but not required.
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