Roche is seeking a Regulatory Submissions professional to lead dossier preparation for moderate‑complexity products and to craft general submission plans for market access. You will apply knowledge of IVDR, FDA, and ISO 13485 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-18808-Ljbffr
📌 Global Regulatory Submissions & Compliance Lead (Madrid)
🏢 Roche
📍 Madrid