Remote Senior Validation
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.
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.