Regulatory Affairs Specialist — Hybrid, Dossier

Overview In this role you support the pharmaceutical manufacturer by preparing and reviewing regulatory dossiers, ensuring compliance, and coordinating documentation for health authority submissions. You will liaise with authorities and clients on changes to manufacturing or control processes, and help implement and train staff on regulatory policies. You...

Overview In this role you support the pharmaceutical manufacturer by preparing and reviewing regulatory dossiers, ensuring compliance, and coordinating documentation for health authority submissions. You will liaise with authorities and clients on changes to manufacturing or control processes, and help implement and train staff on regulatory policies. You...

ManpowerGroup Talent Solutions busca un/a Regulatory Affairs Specialist CMC para el Área de I+D de una multinacional farmacéutica de genéricos de valor añadido, ubicada en Martorelles, Cataluña. La misión es preparar la documentación del Módulo 3 Calidad para nuevas solicitudes, variaciones y cartas de deficiencias.Se exige al menos 5 años de...

Overview In this role you support the pharmaceutical manufacturer by preparing and reviewing regulatory dossiers, ensuring compliance, and coordinating documentation for health authority submissions. You will liaise with authorities and clients on changes to manufacturing or control processes, and help implement and train staff on regulatory policies. You...

Overview In this role you support the pharmaceutical manufacturer by preparing and reviewing regulatory dossiers, ensuring compliance, and coordinating documentation for health authority submissions. You will liaise with authorities and clients on changes to manufacturing or control processes, and help implement and train staff on regulatory policies. You...

Grifols, empresa global del sector salud, busca un especialista IH/Regulatory Affairs para unirse al departamento de Regulatory Affairs Diagnóstico. El/la profesional gestionará expedientes de registro y variaciones, y asesorará sobre requisitos regulatorios a nivel mundial. Las responsabilidades incluyen coordinación con I+D, fabricación y QA,...

Overview In this role you support the pharmaceutical manufacturer by preparing and reviewing regulatory dossiers, ensuring compliance, and coordinating documentation for health authority submissions. You will liaise with authorities and clients on changes to manufacturing or control processes, and help implement and train staff on regulatory policies. You...

Overview In this role you support the pharmaceutical manufacturer by preparing and reviewing regulatory dossiers, ensuring compliance, and coordinating documentation for health authority submissions. You will liaise with authorities and clients on changes to manufacturing or control processes, and help implement and train staff on regulatory policies. You...