Roche is seeking a Regulatory Submissions professional to lead dossier preparation for moderate?complexity products and to craft integral submission plans for market access. You will apply knowledge of IVDR, FDA, and ISO * frameworks to ensure compliant pathways and collaborate with internal teams and external regulators.
With 1+ years in Regulatory Affairs, QA, R&D;, or Clinical Operations, you will use MS Office and EDMS/RIMS to manage documents, drive improvements, and support audits.
#J-*-Ljbffr
📌 Global Regulatory Submissions (Barcelona)
🏢 Roche
📍 Barcelona
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.