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.
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📌 Regulatory Affairs Specialist - Medical Devices (LATAM) (Centro)
🏢 Jobtailor
📍 Centro
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