INDIBA Group is seeking a Regulatory Affairs Specialist to join our Sant Quirze del Vallès office. You will manage regulatory approvals worldwide for medical devices and cosmetics, ensuring compliance and timely submissions.Qualifications include a degree in health sciences or related field, 3+ years in regulatory affairs, and strong knowledge of MDR 2017/745 and ISO 13485. Bilingual Spanish/English is required, with additional languages a plus.
📌 Regulatory Affairs Specialist – Medical Devices (Madrid)
🏢 remoteo
📍 Madrid
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