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 (QC) / Analytical Development Scientist (India)
🏢 EduRun Group
📍 India