Experteer Overview
Sea uno de los primeros solicitantes, lea la descripción completa del puesto a continuación y luego envíe su candidatura para que sea considerada.
In this Barcelona-based on-site role, you support Regulatory Affairs Management (RAM) to obtain and maintain licenses and applications per AstraZeneca standards. You work跨 closely with HA systems, manage regulatory files, and assist with simple submissions and regulatory dispatch planning. You’ll coach RAM members, contribute to process improvements, and act as a point of contact for non-drug project roles. This position offers exposure to HA portals and AZ processes within a collaborative, growth-focused culture.
Compensaciones / Incentivos
• Document management: upload and track regulatory files per AZ procedures
• Plan, prepare, and execute simple submissions; assist planning of regulatory dispatches




• Interface with Health Authority systems for designated tasks (fees, FDA correspondence, EudraLink, EudraPortals)
• Order and track regulatory requirements (Registration samples, CPs, Legal docs, translations)
• Provide cross-group support; act as point of contact or superuser for assigned roles
• Coach, mentor and share knowledge within RAM; contribute to process improvement xqbhyrx
Responsabilidades
• 1–3 years of Regulatory experience in biopharma industry or health authority
• Proficient written and spoken English
• Project management skills
• Experience with document management and tracking databases
• Scientific background in related field
• Knowledge of AZ business processes (preferred)
Requisitos principales
•

📌 Regulatory Affairs Associate (Barcelona)
🏢 AstraZeneca
📍 Barcelona