Recordati is seeking a Regulatory Affairs Associate on a fixed-term contract to join the International Corporate Regulatory Affairs team in Italy. You will manage regulatory activities for SPC medicinal products for human use, including EU marketing authorisations and non-EU submissions.
Responsibilities include preparing and submitting regulatory documentation, coordinating with cross-functional teams, maintaining core dossiers, and monitoring legislation to ensure compliance.
📌 Specialist Regulatory Affairs (Turbigo)
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📍 Turbigo