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In this role, you will support Regulatory Affairs Management in securing and maintaining licenses under AstraZeneca standards. You will interact with Health Authorities and manage regulatory files, ensuring timely submissions and compliant documentation. You’ll contribute to process improvements and share knowledge within the RAM group.

The position blends on-site regulatory tasks in Barcelona with cross-functional collaboration to advance product approvals and lifecycle activities. This is a growth-focused role for a detail-oriented regulatory professional who thrives in a fast-paced, mission-driven environment.

Compensaciones / Incentivos

- Document management and tracking of regulatory files per AZ procedures and regulatory requirements
- Plan, prepare,



and execute simple submissions; assist with regulatory dispatch planning
- Interface with Health Authority systems for tasks like fees, FDA correspondence, and EudraLink
- Order and track regulatory items (e.g., Registration samples, Certificates of Pharmaceutical Product, legal documents, translations)
- Support the group as a point of contact or superuser for non-drug projects
- Provide coaching and knowledge sharing xugodme within RAM
- Contribute to process improvement

Responsabilidades

- 1–3 years of regulatory experience in biopharma, health authority, or relevant field
- Associate's degree in a scientific discipline or related field
- Proficient verbal and written English
- Project management skills
- Experience in document management and tracking databases

Requisitos principales

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📌 Regulatory Affairs Associate (Barcelona)
🏢 AstraZeneca
📍 Barcelona