Job Description The Regulatory Affairs Specialist provide regulatory and operational support across a broad range of activities, ensuring that medicinal products and medical devices, where applicable, remain compliant with Italian and European regulatory requirements throughout their lifecycle. Reporting to the Regulatory Affairs, Quality Assurance & Pharmacovigilance Associate Director, will work closely with internal departments and external stakeholders and will contribute to the maintenance…
Regulatory Specialist
Sobi
IT
🎯 Intermedio🧭 Other🏢 Sanità⏳ 3+ anni🗣️ Italiano
Competenze richieste
regulatory affairsgmpiso-13485pharmacovigilanceeuropean medical device regulations
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