A pharmaceutical company in Alcobendas seeks a Regulatory Affairs Specialist responsible for general regulatory submissions and compliance with regulations. The ideal candidate must have at least 3 years of experience in regulatory roles, strong knowledge of EMA and ICH guidelines, and be fluent in English. Responsibilities include preparing regulatory dossiers, collaborating with health authorities, and supporting product registrations. This position plays a crucial role in ensuring product availability and compliance in the market.
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