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Bristol Myers Squibb

Bogotá / Global

Senior Regulatory Documentation Specialist

Job Description

Bristol Myers Squibb seeks a Senior Documentation Specialist to independently manage eDMS processes, formatting, and publishing of regulatory documents. You will collaborate with GSRD and external authors, ensuring submission readiness across protocol and CSR content.

The role emphasizes meticulous document control, cross-functional coordination, and continuous improvement of regulatory workflows within a fast‑paced environment.

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