Post Market Surveillance Specialist supporting regulatory compliance for medical devices across EU markets. Evaluate incoming complaints and maintain records in electronic database following company procedures
Collect, trend, and escalate post-market surveillance data to appropriate regulatory agencies
Knowledge of EU MDR 2017/745, UK Medical Devices Regulations, and Swiss Medical Devices Ordinance
~ Bachelor's degree or Swiss CFC in Health Sciences preferred
~6 months to 2 years complaint handling experience in medical devices
~ Fluent in written and spoken English, Spanish, and Portuguese
~ Attention to detail with emphasis on accuracy and data completeness
~ Proficiency with Microsoft Office suite and general computer literacy
📌 CRM Marketer (España)
🏢 Intuitive Surgical
📍 España
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