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. You will coordinate risk activities across development and legacy devices and partner with Human Factors to ensure user safety.The ideal candidate has 2+ years in regulated medical devices, experience in usability engineering, and a Master’s in Engineering. Fluent English is required, with opportunities for growth in a general company.#J-18808-Ljbffr
📌 Risk Manager, Medical Devices & Regulatory (Madrid)
🏢 Sinclair
📍 Madrid
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