Pharma CSV Engineer: Validation & Compliance Expert

biotech in Singapore seeks a CSV Validation Specialist to develop and review validation plans, IQ/OQ/PQ protocols, and related reports for computerized systems across manufacturing processes.

You will perform risk assessments, ensure compliance with FDA/EU guidelines, collaborate with IT, QA, and Manufacturing, manage change controls, and support regulatory audits. A bachelor’s degree and 5–8 years in CSV are required.