MedTech Clinical Evaluation (España)

MedTech Clinical Evaluation (España)

07 nov
|
MDx CRO
|
España

07 nov

MDx CRO

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.

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You will prepare CERs, CEPs, and EU MDR‑compliant technical documentation, support US regulatory submissions, and collaborate with multidisciplinary teams across international projects. xqbhyrx

The role offers autonomy, exposure to leading MedTech clients, and opportunities for professional development

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Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.

📌 MedTech Clinical Evaluation (España)
🏢 MDx CRO
📍 España

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