The Regulatory Affairs Specialist II, LATAM Operations & Submissions, will support regulatory strategy, regulatory operations and submission planning across LATAM within QARA International. This role provides regulatory guidance, readiness and partners with local affiliates to enable compliant product registrations and lifecycle management across international markets.
Based in Mexico City or Bogota, you will contribute to integral regulatory processes, drive collaboration, and help ensure timely
📌 LATAM Regulatory Affairs Specialist II — Submissions (Ciudad de México)
🏢 Johnson & Johnson MedTech
📍 Ciudad de México
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