Chiesi is seeking a senior expert to lead validation, qualification, and compliance activities at the Parma site. You will oversee end-to-end validation programs, ensure Data Integrity, and coordinate cross-functional teams for multiple projects within a GMP framework.
With 8–10 years in pharma manufacturing, you will drive regulatory readiness, support inspections, and shape the site’s validation strategies in alignment with EU and FDA requirements.
📌 Remote Senior Validation (Lazio)
🏢 Chiesi
📍 Lazio