Cordis in Mexico is seeking a Regulatory Affairs Specialist II to support regulatory submissions, registrations and lifecycle activities for our cardiovascular devices. You will work closely with Manufacturing, Quality, Engineering and Product Development at the Juarez site to ensure integral regulatory compliance.
The role requires 3+ years in regulatory affairs, a Bachelor's degree, and knowledge of FDA, EU MDR, ISO 13485 and MDSAP.
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📌 Regulatory Affairs Specialist II – Medical Devices (México)
🏢 Cordis
📍 México