About this role
Regulatory Affairs Specialist at Recordati Industria Chimica. Location: Milano, Lombardy, Italy. Role: preparing submissions, managing dossiers, coordinating affiliates Requirements: Scientific degree required, master in regulatory affairs preferred; >5 years regulatory affairs experience in multinational pharma or consulting; experience with EU centralized/decentralized procedures, OTC lifecycle management, and regulatory submissions; fluent English. Category: Legal and Compliance Seniority: Senior Level Tools: RIMS, DMS, eCTD platform Commitment: Full Time Workplace: Hybrid Languages: English