Bristol Myers Squibb is seeking a Senior Documentation Specialist to independently manage eDMS processes, publish regulatory documents, and collaborate with GSRD and external authors. The role involves mentoring, ensuring submission-ready formatting, and coordinating protocol and CSR
At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to
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,
At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to
At Bristol Myers Squibb, our employees often ask, Who are you working for?, a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines