Bristol Myers Squibb is seeking a lead End-to-End Documentation Specialist to steer regulatory filings and HA responses. You will guide GSRD and external authors on eDMS, model documents, and submission-ready formatting for protocol and submission documents, ensuring timely, compliant deliverables across multiple submission types.
The role requires a BS/BA with 4+ years in regulatory documentation, strong Acrobat and ISI Toolbox expertise, and proven ability to train teams and manage timelines
📌 Global Regulatory Documentation Lead (Bogotá)
🏢 Biopharma Careers
📍 Bogotá
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