Sinclair is seeking a Risk Manager in Spain to lead risk management for medical devices and aesthetic products, aligning with ISO 14971, MDR and ISO 13485.
Las cualificaciones, habilidades y toda la experiencia relevante necesaria para este puesto se pueden encontrar en la descripción completa a continuación.
You will coordinate risk activities across development and legacy devices and partner with Human Factors to ensure user safety.
The idóneo candidate has 2+ years in regulated medical devices, experience in usability engineering, and a Master’s in Engineering. xhfqzwm
Fluent English is required, with opportunities for growth in a global company.
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📌 Risk Manager, Medical Devices & Regulatory (Río Henares)
🏢 Sinclair
📍 Río Henares
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