Full-time

Especialista de Asuntos Regulatorios

Posted by Abbott Laboratories • June 13, 2026

📍 Remote, Remote, Colombia
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Description

Location

Bogotá, Colombia

Responsibilities

  • Receive data from affiliates and consolidate reports for regional teams.
  • Include updates for the global plan in the template based on information received from RA leaders.
  • Follow up with QA, clinical, and TPM areas to request modules ensuring dossiers can be prepared by RA specialists.
  • Keep the RA database 2024 plan updated according to approvals or submissions reported by affiliates.
  • Ensure change controls activities are uploaded in the system and reminder notifications sent to owners to close the change control.
  • Notify deviations to their respective due dates.
  • Track indication updates in the risk assessment for labeling distribution.
  • Verify inserts versions approved by manufacturing and receiving countries.
  • Upload dossiers for submission and validate their visualization in DARIUS.
  • Ensure correct filling of information in DARIU...

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