Solo Quedan 24h: Regulatory Affairs
hace 3 semanas
Objetivos del Puesto
- Colaborar en la obtención y seguimiento de autorizaciones de comercialización y sus modificaciones.
- Preparar, revisar y presentar expedientes regulatorios (nuevos registros, revalidaciones, variaciones, etc.).
- Elaborar documentación requerida para las agencias reguladoras y seguir las solicitudes.
- Colaborar con otras áreas para garantizar el cumplimiento normativo de productos en mercados nacionales e internacionales.
- Actualizar los sistemas de seguimiento interno y externo de información regulatoria.
- Comunicarse con autoridades sanitarias y equipos globales de asuntos regulatorios.
Requisitos del Cargo
- Grado o Licenciatura en Ciencias de la Salud (Farmacia, Veterinaria, Biología, Biotecnología u otros afines).
- Postgrado o máster en Industria Farmacéutica y/o Asuntos Regulatorios (valorable).
- Experiencia previa en el área de Regulatory Affairs o consultoría (valorable).
- Conocimientos básicos sobre regulación de medicamentos veterinarios en la Unión Europea.
- Nivel de inglés intermedio-avanzado .
- Conocimiento de francés y/o experiencia internacional (se valorará).
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