Location
bogotá, bogotá, distrito capital, Colombia
Posted
June 29, 2026
Job Description
Emmes is looking for a Controlled Documents Specialist to manage the document lifecycle within the Veeva Quality platform. The role emphasizes compliance with regulatory requirements and quality management standards.
You will oversee document creation, review, and approval while supporting audit readiness and maintaining accurate metadata. A bachelor's degree in Life Sciences and 1-3 years of experience in regulated environments are required.
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