Regulatory Compliance Auditor Subject Matter Expert -AI Model Evaluation

About the role

Remote | United States | Project-Based Independent Contractor

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

Help Shape the Future of AI in Pharmaceutical

What if your expertise in pharmaceutical auditing, regulatory compliance, quality systems, and inspection readiness could help artificial intelligence better understand compliance risks, regulatory expectations, and audit 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 Regulatory Compliance Auditors who can apply their auditing expertise, compliance knowledge, and industry experience to evaluate AI-generated pharmaceutical content.

This isn't a traditional auditing position. You won't be conducting supplier audits, preparing organizations for regulatory inspections, or managing compliance programs. Instead, you'll evaluate complex compliance and audit-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.

The Opportunity

As a Regulatory Compliance Auditor 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 auditing, quality, manufacturing, compliance, supplier oversight, and inspection-readiness scenarios, identify errors or unsupported conclusions, and provide expert feedback grounded in regulatory requirements, audit principles, and pharmaceutical industry best practices.

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

What You'll Do

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.

Why Join Volga Partners?

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.

Compensation:

Volga Partners offers project-based hourly compensation based on specialization, relevant experience, professional qualifications, geographic location, and assignment requirements.

Regulatory Compliance Auditor Subject Matter Experts: $25-$50 USD/hour

Compensation may vary based on experience level, area of expertise, and task complexity.

Project Details

Engagement Type: Project-based independent contractor

Work Arrangement: Remote

Primary Location: United States preferred

Additional Markets: Professionals outside the United States may be considered if they possess substantial U.S. pharmaceutical industry experience

Schedule: Variable and assignment-based

Project Type: Pharmaceutical AI content evaluation

Project Duration: Based on project requirements and assignment availability

Selection Process: Qualified candidates may be required to complete screening questions and evaluation exercises prior to project selection

Specific assignments, schedules, workloads, and project dates will be communicated as they are confirmed. Hours and future assignments are not guaranteed.

Bring Your Pharmaceutical Expertise to the Future of AI

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

Who We're Looking For

We're seeking experienced Regulatory Affairs professionals in the Pharmaceutical world who bring practical industry expertise and are comfortable reviewing technical information, exercising independent judgment, and clearly explaining their conclusions.

Required Qualifications

Minimum of 4 years of professional experience in Regulatory Compliance, Quality Auditing, GMP Auditing, Supplier Quality, Quality Assurance, or related pharmaceutical functions

Bachelor's degree or higher in Pharmacy, Pharmaceutical Sciences, Chemistry, Biotechnology, Engineering, Life Sciences, Regulatory Affairs, or a related discipline

Experience conducting or participating in GMP audits, supplier audits, compliance inspections, or quality system assessments

Strong knowledge of FDA regulations, GMP requirements, and relevant ICH guidelines

Experience evaluating quality systems, compliance programs, and corrective action plans

Familiarity with audit planning, execution, reporting, and CAPA verification activities

Experience reviewing quality, manufacturing, laboratory, or regulatory documentation

Ability to critically evaluate technical and compliance-related 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 Qualifications

We encourage applications from professionals with backgrounds such as:

Lead Auditor certification or equivalent auditing credentials

PharmD, MS, MBA, PhD, or other advanced scientific credentials

Experience conducting supplier, contract manufacturer, or third-party audits

Experience supporting FDA, EMA, MHRA, Health Canada, or international regulatory inspections

Experience leading compliance remediation and CAPA effectiveness programs

Knowledge of GMP, GDP, GLP, and GCP requirements

Experience performing risk-based auditing and compliance gap assessments

Experience evaluating Quality Management Systems (QMS)

Experience collaborating with Manufacturing, Quality Assurance, Regulatory Affairs, Validation, and Technical Operations teams

Experience with technical writing, audit reporting, or compliance documentation review

Familiarity with AI evaluation, data annotation, or quality review activities

Experience with AI model evaluation, large language models (LLMs), research, or structured quality assessments is beneficial but not required.

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