Regulatory Affairs Lead, Medical Devices CE/MDR

4 giorni fa


Roma, Italia Vantive Manufacturing A tempo pieno

A leading medical device firm in Italy is seeking a Regulatory Affairs professional to support CE marking activities for medical devices. The role involves ensuring regulatory compliance, developing strategies, and collaborating with cross-functional teams. Ideal candidates will have 3-5 years of experience in Regulatory Affairs and possess a good understanding of CE marking regulations. This full-time position offers the chance to make a significant impact in the medical device industry.#J-18808-Ljbffr



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