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. #J-18808-Ljbffr
Remote Veeva Controlled Documents Specialist
EMMES
Bogotá, Bogotá
Publicado hace 11 días
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