MedTech Clinical Evaluation & Regulatory Docs Expert (Remote) (Madrid)

MedTech Clinical Evaluation & Regulatory Docs Expert (Remote) (Madrid)

07 nov
|
MDx CRO
|
Madrid

07 nov

MDx CRO

Madrid

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. You will prepare CERs, CEPs, and EU MDR‑compliant technical documentation, support US regulatory submissions, and collaborate with multidisciplinary teams across international projects. The role offers autonomy, exposure to leading MedTech clients, and opportunities for professional development

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📌 MedTech Clinical Evaluation & Regulatory Docs Expert (Remote) (Madrid)
🏢 MDx CRO
📍 Madrid

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