09 nov
|
Roche
|
Barcelona
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.
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📌 Global Regulatory Submissions (Barcelona)
🏢 Roche
📍 Barcelona