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.
Por favor, presente su candidatura sin demora si su perfil encaja bien con este puesto, debido al alto nivel de interés.
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. xhfqzwm
Flexibility for time zone differences is required.
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