About this role
Regulatory Affairs CMC Specialist at Recordati Industria Chimica. Location: Milan, Lombardy, Italy. Role: writing modules, assessing gaps, conducting assessments Requirements: 3+ years CMC regulatory affairs experience; degree in chemistry, pharmacy or biotechnology; knowledge of GMP/ICH/EMA/WHO guidance; ability to prepare Module 3 dossiers and perform gap analyses; fluent English. Category: Research and Development (R&D) Seniority: Mid Level Tools: CTD, GMP, ICH, Eur. Ph. Commitment: Full Time Workplace: Hybrid Languages: English