Carestream Healthcare International Company Limited seeks a Regulatory Affairs professional in Mexico to lead product registrations across LATAM. You will coordinate with Health Authorities, manage dossiers, and guide internal teams on regulatory requirements. The role requires 5+ years in medical devices or pharma, experience with LATAM regulations, and strong project management with English and Spanish fluency. #J-18808-Ljbffr
📌 Regulatory affairs specialist - medical devices (latam) (Centro Tular)
🏢 Jobtailor
📍 Centro Tular
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