Recordati is seeking a Regulatory Affairs Specialist to join their International Corporate Regulatory Affairs team in Turbigo, Italy. The successful candidate will manage regulatory activities for SPC medicinal products and prepare submissions to Health Authorities. A scientific degree is required, along with over 5 years of experience in Regulatory Affairs within multinational firms. Proficiency in English is essential, along with a proactive mindset and strong communication skills. This role offers the chance to impact a dynamic international environment.
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📌 Global Regulatory Affairs Specialist (Bardi)
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