A leading pharmaceutical company in Madrid is looking for a Regulatory Affairs Specialist to support general regulatory submissions and ensure compliance with regulatory requirements. The role involves preparing regulatory dossiers, collaborating with cross-functional teams, and maintaining high-quality regulatory documentation. This position requires a minimum of 3 years of experience in regulatory roles, strong knowledge of EMA and ICH regulations, and fluency in English. Join us to make a significant impact on product availability and regulatory compliance.
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