remoteo
Regulatory Affairs Officer
- Híbrido
- Tiempo completo
- Contrato
... experience in regulatory affairs within a medical device or pharmaceutical company, or a regulatory consultancy. - In-depth knowledge of medical device legislation, particularly the Medical Device Regulation (MDR) 2017/745 and ISO 13485. Experience with devices covered by Annex XVI, relating to products without an intended medical ...
San Quirico de Tarrasa, España