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 integral 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.
#J-18808-Ljbffr
📌 Regulatory Affairs Specialist (España)
🏢 Msd
📍 España
Postulate a este anuncio
Muestra tus habilidades a la empresa, rellenar el formulario y deja un toque personal en la carta, ayudará el reclutador en la elección del candidato.