Roche is seeking a Regulatory Affairs professional to oversee submission compilation for complex diagnostics products and manage cross‑functional, general regulatory strategies from this Sant Cugat location. You will work with teams across regions to influence timelines and approvals, applying strong regulatory knowledge and stakeholder engagement. The role emphasizes adapting strategies to regulatory changes, maintaining high integrity, and collaborating to ensure patient access and compliance
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📌 Global Regulatory Affairs Lead — Diagnostics & Submissions (Madrid)
🏢 Roche
📍 Madrid
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