10 nov
|
Confidential
|
España
10 nov
Confidential
España
MDx CRO is seeking an experienced Regulatory Affairs professional with a strong focus on clinical evaluation, medical writing and technical documentation for medical devices to join our consulting team. ¿Quiere enviar su solicitud? Lea toda la información sobre este puesto a continuación y luego pulse el botón de solicitar. You will prepare CERs, CEPs, and EU MDR‐compliant technical documentation, support US regulatory submissions, and collaborate with multidisciplinary teams across international projects. xcskxlj The role offers autonomy, exposure to leading MedTech clients, and opportunities for professional development #J-18808-Ljbffr Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.
📌 MedTech Clinical Evaluation (España)
🏢 Confidential
📍 España