Eusa Pharma in Spoleto, Italy seeks a Regulatory Affairs Specialist to manage regulatory activities for SPC medicinal products for human use. The role covers EU authorisations via CP/MRP/DCP and regional regulatory support, requiring strong collaboration with cross-functional teams.
Candidates should have 5+ years in regulatory affairs within multinational pharma, with expertise in EU procedures and OTC lifecycle management, plus a high degree of autonomy.
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