EU Device Labeling Regulatory Lead

A leading pharmaceutical company in Madrid is looking for a Regulatory Affairs Specialist to provide advice on EU MDR and ensure compliance with labeling requirements for assigned products. The candidate will collaborate with global teams to analyze competitor labeling and maintain active awareness of relevant EU legislation. Applicants should have 5-7 years of experience in Regulatory or R&D, with strong project management and communication skills. Flexibility for time zone differences is required.
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