MSD in Spain is seeking a Regulatory Affairs Specialist to manage regulatory lifecycle for oncology and vaccines portfolios. You will coordinate with local, regional and general teams and engage with AEMPS to ensure timely access to innovative therapies.
You will prepare MA applications, manage variations and renewals, and ensure labeling and SmPCs comply with EU and Spanish guidance. Strong Spanish/English skills and 1–2 years of experience are required.
📌 Regulatory Affairs Specialist – Oncology (Madrid)
🏢 Msd
📍 Madrid