CSV Engineer - Milan, Italy - 12 Month Contract
Our client is a leading global CDMO providing end‐to‐end pharmaceutical development and manufacturing services. Its expertise spans from APIs to finished drug products, supporting pharmaceutical and biotech companies in bringing medicines to market. What You'll Do Draft and review validation documentation, including technical reports, for computerised system validations.
Review SOPs, specifications, and production documents in compliance with GMP and company procedures.
Review validation activities of computerised systems used in different departments, ensuring consistency with GMP requirements.
Write and review procedures related to computerised system validation.
Support,



within the validation group, operators performing tests to ensure computer system validation activities.
High school diploma and/or degree in scientific subjects.
Extensive experience in a similar role.
Good knowledge of GMP.
Good knowledge of English for documentation purposes and participation in customer and regulatory audits.
Client‐Server architectures, standalone systems, backup & restore, access and profile management, laboratory systems (LIMS; Empower), production systems (SCADA).

📌 Ingénieur diplômé (Italia)
🏢 QCS Staffing
📍 Italia