Aortyx seeks a Regulatory Affairs Specialist to drive regulatory strategy for medical devices in Europe and the US.
Compruebe a continuación si tiene lo necesario para esta posibilidad y, si es así, envíe su solicitud lo antes posible.
You will develop and maintain the regulatory roadmap, manage risk analyses, and guide R&D; teams to ensure compliance across product lifecycles.
Collaboration with labs, consultants, and authorities is essential to navigate EU MDR and FDA requirements. xqbhyrx
You will prepare and review regulatory submissions, oversee labeling, and support audits and inspections.
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📌 Regulatory Affairs Lead, Medical Devices (Barcelona)
🏢 Aortyx
📍 Barcelona
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