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Regulatory Affairs Associate (Colombia)

Regulatory Affairs Associate (Colombia)

Location Colombia
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Job ID
CB1060
Date posted
04/08/2026
Category
Regulatory Affairs
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Contract: 12 months

Location: Bogota, Colombia 

Summary / Purpose of the Role
The Regulatory Affairs Specialist is responsible for providing operational and administrative support to Regulatory Affairs activities for the medical devices portfolio in Colombia. Guided by senior Regulatory Affairs professionals, this role supports regulatory documentation management, systems updates, and project coordination to ensure compliance with applicable regulations and internal requirements.

Key Responsibilities

  • Support collection and tracking of regulatory documentation for INVIMA submissions

  • Perform initial completeness checks of regulatory documentation

  • Maintain organized and audit-ready regulatory files

  • Assist in executing approved regulatory plans under supervision

  • Update regulatory systems, databases, and trackers

  • Support the coordination of regulatory projects and cross-functional requests

  • Ensure compliance with company policies and procedures

Qualifications

  • Bachelor’s degree in Life Sciences, Engineering, Pharmacy, or related field

  • Entry-level role; prior internships or exposure to regulated environments are a plus

  • Basic understanding of Colombian medical device regulations (Decree 4725 of 2005)

  • Proficiency in Microsoft Office tools

  • Strong attention to detail and willingness to learn

Core Competencies & Behaviors

  • Learning agility and curiosity

  • Attention to detail

  • Accountability for assigned tasks

  • Collaboration with cross-functional teams

  • Proactive communication

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