Senior eDMS & Regulatory Publishing Specialist
Bristol-Myers Squibb
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.
Ideal 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,
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