Global Regulatory Affairs Lead – Ivd/Software

Roche is seeking an International Regulatory Affairs Professional to drive regulatory strategies for global 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 #J-18808-Ljbffr