INDIBA Group in Sant Quirze del Vallès is looking for a Regulatory Affairs Specialist to obtain, update and maintain worldwide regulatory approvals for medical devices and cosmetics. You will work across regions to ensure compliance with regulatory requirements and maintain the quality systems in place.The role requires a degree in a health sciences field and at least three years of regulatory affairs experience, with strong knowledge of MDR 2017/745, ISO 13485 and experience with US FDA
📌 Regulatory Affairs Specialist – Medical Devices (Vallés)
🏢 Indiba Group
📍 Vallés
Postulate a este anuncio
Muestra tus habilidades a la empresa, rellenar el formulario y deja un toque personal en la carta, ayudará el reclutador en la elección del candidato.