We are looking for US Pharma-Quality Control (QC) / Analytical Development Scientist to work on an AI based project of our client. Project: US Pharma Experience Required: 5+ years in analytical testing, method validation, stability testing, specifications Pay: $15
- $25 (Based on Experience and Profile) Number of hours: Minimum 4-5hours/day Duration
- 2-3 days(can be extended)

Skills:
Mandatory to have US Pharma experience Project Start Date: Immediate Role Overview:The project aims to evaluate dataset accuracy across three dimensions—prompts, rubrics, and artifacts—with a focus on scientific and regulatory correctness, source-document consistency, and benchmark quality. Education Background: Bachelor's or Master's in Pharmacy, Pharmaceutical Sciences, Chemistry, Biotechnology, Chemical Engineering, or related fields.



PharmD or PhD preferred for specialized roles. Required

Skills:
Regulatory knowledge: Working knowledge of FDA 21 CFR Parts 210/211, ICH Q7–Q12, GMP, and applicable FDA/EMA guidance Documentation expertise: Experience with SOPs, specifications, batch records, deviation reports, CAPA, change controls, or CTD Module 3. Evaluation

skills:
Robust written English and ability to assess AI-generated responses against detailed rubrics. Analytical

skills:
Ability to reconcile conflicting records, identify authoritative documents, and provide evidence-backed decisions.

📌 US Pharma-Quality Control (India)
🏢 EduRun Group
📍 India