12 ago
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Bristol-Myers Squibb
|
Bogotá
12 ago
Bristol-Myers Squibb
Bogotá
Bristol Myers Squibb in Bogotá, Colombia seeks a Senior Documentation Specialist to independently manage eDMS processes and publishing of regulatory documents. You will mentor GSRD staff and external authors, ensuring submission readiness and high-quality output aligned with ICH and eCTD standards.
The role requires a BS/BA with 2–4 years of regulatory documentation experience, strong candidate management, and excellent cross-functional collaboration.
📌 Senior Regulatory Documentation Lead (Bogotá)
🏢 Bristol-Myers Squibb
📍 Bogotá