16 oct
|
Indiba K-Laser
|
Madrid
16 oct
Indiba K-Laser
Madrid
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 (Hybrid) (Madrid)
🏢 Indiba K-Laser
📍 Madrid