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 (Madrid)
🏢 Roche
📍 Madrid