Bristol Myers Squibb is seeking a Senior Documentation Specialist in Bogote1 to independently manage eDMS processes and publication of regulatory documents. You will mentor colleagues, collaborate with GSRD and external authors, and define submission-ready requirements for protocol and submission documents.
Idóneo candidates have a BS/BA with 2–4 years of regulatory documentation experience, strong Acrobat/ISI toolbox skills, and experience with document management systems to support efficient,