15 oct
|
Intuitive
|
Madrid
Intuitive seeks a Regulatory Affairs Specialist to provide advanced regulatory support for NPD, market expansion, and sustaining operations across EMEA.
Las cualificaciones, habilidades y toda la experiencia relevante necesaria para este puesto se pueden encontrar en la descripción completa a continuación.
Must master EU MDR, ISO 13485, and RoHS, and lead regulatory submissions with cross-functional teams.
The role requires collaboration with Product Lifecycle Management, Supply Chain, Marketing, and Commercial groups to align regulatory requirements with business goals. xcskxlj
Strong project management and integral regulatory knowledge are essential.
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📌 EMEA Regulatory Affairs Specialist (Medical Devices) (Madrid)
🏢 Intuitive
📍 Madrid