Roche is seeking an International Regulatory Affairs Professional to drive regulatory strategies for general IVD/MD instrument and software submissions. You will ensure compliance with international requirements and collaborate with R&D;, Quality, and Clinical teams to advance regulatory initiatives.You bring a bachelor’s degree in life sciences and 5–7 years of Regulatory Affairs experience, along with strong organizational skills and the ability to manage multiple projects in a fast-paced
📌 Global Regulatory Affairs Lead – Ivd/Software (España)
🏢 Roche
📍 España
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