Global IVD Regulatory Affairs Project Manager (Hybrid)
Roche
Roche in New Jersey seeks an experienced Regulatory Affairs professional to support global medical diagnostic products. The role involves registering and addressing affiliate questions, improving processes with RPA, and ensuring regulatory compliance across US and international markets. You will participate in submissions (CE, PMA, 510(k)), maintain technical files, and work with cross‑functional teams on labeling, documentation, and product changes. Hybrid work arrangement included. #J-18808-Ljbffr Roche
Vacancy posted 4 days ago
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