Regulatory Affairs Specialist – Medical Devices

Hace 5 días

Barcelona, Cataluña, España INDIBA K-LASER Jornada completa
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. #J-18808-Ljbffr