Global IVD Regulatory Project Lead
Roche
Roche – Tucson, AZ – is seeking an experienced regulatory affairs professional to support regulatory activities for a broad range of diagnostic products. You will review changes, maintain filings, and help ensure compliance across US and international markets. The role requires handling PMA/510(k) submissions, CE registrations, and ongoing regulatory documentation while coordinating with researchers, physicians, and regulatory authorities. Hybrid work applies. #J-18808-Ljbffr Roche
Vacancy posted 13 hours ago
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