Key Responsibilities:
Conduct GCP audits (e.g., site, vendor, document, system audits).
Ensure clinical trial compliance with FDA, EMA, ICH, and other regulatory bodies.
Identify quality issues and collaborate on corrective/preventive actions (CAPAs).
Support inspection readiness and regulatory agency audits.
Maintain quality documentation and QA metrics.
Job Type: Full-time
Pay: ₹330,000.00 - ₹650,000.00 per year
Benefits:
Health insurance
Work Location: In person