Bristol Myers Squibb REGULATORY AFFAIRS ANALYST in SÃO PAULO, United States

• Understands and fulfills current and local regulations and internal policies while assessing, planning and executing regulatory processes• Prepares regulatory low-mid complexity filings w/o major supervision• Assist on preparation of major filings under certain supervision• Formulates mitigation plans for regular issues, identifies impacted areas and processes and drives the process under supervision• Updates local labeling components, review and approve promotional materials in full adherence to the Company Core Data Sheets (CCDS), BMS policies and local applicable regulations. • Timely and accurately feeds systems, databases and archives.• Drives contacts and consultations with HA within his/her scope• Supports preparation and deployment of HA interactions• Participates in Trade Association meetings• Develops its own working plan taking accountability for timely completion of assigned functions• Takes full accountability for timely delivery of quality results, with reasonable sense of urgency and priority

We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.

Bristol-Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.