Skip to content

Domain Experts

Pharmaceutical Quality Assurance Subject Matter Expert - AI Model Evaluation

Volga Partners logoVolga Partners$20–$50/hrRemote in United StatesContractPosted 1d ago
Apply on Volga Partners (opens the job details)Is Volga Partners legit? Pay and reviews

The middle of its range, $35/hr, is below the $70/hr median of the Law, Medicine & Finance roles open now, whose typical pay runs $40–$150/hr. How that pay moves week by week is in our research on Law, Medicine & Finance work.

Half of all Law, Medicine & Finance roles come down within 29.5 days of being listed, and 51.4% are still up after four weeks. This one was posted 1 day ago.

About the role

Help Shape the Future of AI in Pharmaceutical

What if your expertise in pharmaceutical quality systems, GMP compliance, and quality oversight could help artificial intelligence better understand quality management practices and regulatory expectations?

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

We're seeking Pharmaceutical Quality Assurance professionals who can apply their expertise in quality systems, compliance, investigations, and GMP operations to evaluate AI-generated pharmaceutical content.

This isn't a traditional position. You won't be preparing submissions, managing product registrations, or interacting with health authorities. Instead, you'll evaluate complex regulatory 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 Pharmaceutical Quality Assurance Subject Matter Expert (SME), you'll serve as a subject matter evaluator, helping assess the quality, accuracy, and reasoning of AI-generated pharmaceutical and biotechnology content.

You'll analyze scientific, regulatory, manufacturing, and compliance-related scenarios, identify errors or unsupported conclusions, and provide expert feedback grounded in industry standards, regulatory frameworks, and professional judgment.

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.

Apply Your Industry Expertise in a New Way

Use the knowledge you've developed throughout your regulatory affairs 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 availability.

Explore the Future of Pharmaceutical Technology

Gain experience contributing to AI evaluation initiatives while leveraging your existing regulatory expertise.

No AI Background Required

We're looking for professionals who can identify regulatory risks, evaluate compliance considerations, and communicate expert assessments clearly.

Compensation

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

Pharmaceutical Quality Assurance Subject Matter Expert (SME),: $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 regulatory professional who enjoys analyzing complex compliance requirements, evaluating technical information, and applying regulatory judgment, 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.

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 4 years of pharmaceutical QA experience
  • Bachelor's degree or higher in Pharmacy, Pharmaceutical Sciences, Chemistry, Biotechnology, or a related discipline
  • Experience with GMP-regulated environments
  • Understanding of QMS, CAPA, deviations, and change control systems
  • Strong analytical and technical review skills
  • 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

We encourage applications from professionals with backgrounds such as

  • Quality Systems leadership experience
  • Inspection readiness experience
  • Supplier quality management experience
  • ASQ certification or equivalent quality credentials
  • Experience managing post-approval changes and variations
  • Technical writing or document review experience
  • 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.

Where you can work

This role is 100% remote, for applicants located in United States.

From Volga Partners's job posting, checked 30 Oct 2026.

Apply on Volga Partners (opens the job details)

The application

Your details, CV and LinkedIn, then 26 questions (2 written).

Have readyCVLinkedInPhoto (optional)Cover letter (optional)
  1. 1.
    HeadlineShort answer · optional
  2. 2.
    EducationShort answer · optional
  3. 3.
    ExperienceShort answer · optional
  4. 4.
    SummaryWritten answer · optional
  5. 5.
    Are you currently based in the United States?Yes or no
  6. 6.
    Are you authorized to work in the United States?Yes or no
  7. 7.
    If yes, which state are you currently residing?Short answer
  8. 8.
    How many years of professional experience do you have in the regulated pharmaceutical or biotechnology industry?Pick any: 6583041 · 6583042 · 6583043 · 6583044
  9. 9.
    Which pharmaceutical specialties match your professional experience?Pick any (9 options)
  10. 10.
    Which settings account for your relevant professional experience?Pick any (9 options)
  11. 11.
    What is your highest completed qualification relevant to this role?Pick any: 6583063 · 6583064 · 6583065 · 6583066 · 6583067 · 6583068
  12. 12.
    Employment supporting U.S. pharmaceutical / biotechnology operationsPick any: 6583069 · 6583070 · 6583071 · 6583072 · 6583073 · 6583074
  13. 13.
    Have you previously evaluated AI-generated medical content, participated in medical AI training, or performed structured clinical quality reviews?Pick any: 6583075 · 6583076 · 6583077 · 6583078
  14. 14.
    Which standards have you applied in your professional work?Pick any (8 options)
  15. 15.
    Where will you be physically located while performing this project?Pick any: 6583087 · 6583088
  16. 16.
    If outside Unites States, provide which country.Short answer
  17. 17.
    Can you complete selection and onboarding steps and be available for potential participation beginning Monday, October 26, 2026?Pick one: 6583089 · 6583090 · 6583091 · 6583092
  18. 18.
    Which days can you regularly accept on-call assignments?Pick any (7 options)
  19. 19.
    How many hours per week could you make available if assignments are offered?Pick any: 6583100 · 6583101 · 6583102 · 6583103 · 6583104
  20. 20.
    What hourly rate in USD would you accept for this content evaluation scope?Pick any: 6583105 · 6583106 · 6583107 · 6583108 · 6583109
  21. 21.
    Which relevant review activities have you performed? Select All That ApplyPick any (7 options)
  22. 22.
    List your ongoing working windows and time zone. Include any scheduling restrictions.Written answer
  23. 23.
    Are you comfortable evaluating AI-generated medical responses, identifying inaccuracies, and providing structured written feedback in English?Yes or no
  24. 24.
    Must understand and accept that this is a task-based, freelance role. [Task-Based Project Scope] This is a freelance, task-based role designed for those seeking supplemental income. It’s essential to understand the nature of freelance work-Yes or no
  25. 25.
    Do you understand this is an on-call freelance project, with assignments subject to confirmation and task availability rather than guaranteed weekly hours?Yes or no
  26. 26.
    Are you willing to work remotely as a project-based independent contractor, with hours and assignments varying according to project requirements?Yes or no

From Volga Partners's apply page, checked 30 Oct 2026.

About Volga Partners

An AI data company that hires on-call subject-matter experts and language reviewers for AI evaluation projects; US expert roles pay $35 to $60 an hour, healthcare students and trainees $15 to $35 (its postings, 27 Oct 2026).

How it pays: Not stated beyond the hourly rate; US expert roles are 1099 independent contracts, and a shortlisted candidate completes a trial task that is paid only if it meets the standard.

Volga Partners jobs with full postings Every open Volga Partners role Read the full Volga Partners review

Similar open roles

Some links on AITraining.jobs are referral links. If you sign up through one, AITraining.jobs may earn a commission at no extra cost to you. It never changes what a platform pays you. A role at a platform that pays us a referral fee weighs more in this order.

A licensed or credentialed professional?

One profile for every AI training platform. Companies ask us for people with a specific language, country or credential: add yours once, and when a role fits, we introduce you, only with your yes. Free.

Create my profile

Get new Volga Partners roles by email

We check the Volga Partners job board every hour and email you its newest roles each week, plus similar paid roles elsewhere. Free, unsubscribe anytime.