A global biopharmaceutical company is seeking a GRA Device Associate to contribute to regulatory strategies for in-vitro diagnostics. The role involves partnering with the Device Regulatory Lead, providing regulatory guidance, and managing submissions. Ideal candidates have 6+ years in the pharmaceutical or medical device industry with strong IVD regulatory experience. Duties also include interacting with health authorities and ensuring compliance while navigating complex regulatory landscapes. Join us to help improve patient access to innovative therapies through regulatory expertise.
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