Bristol Myers Squibb Regulatory Analyst in SÃO PAULO, United States

The Regulatory Affairs area is strategic for the growth of the company. Through regulatory processes with ANVISA, the company expands and renews its portfolio. The regulatory environment is constantly changing, requiring companies to be ready to anticipate them, analyze their impacts, plan and implement them in a timely and effective manner. In addition, the Regulatory Affairs area is also responsible for ensuring that the company complies with the applicable health regulations in order to continue business, avoid penalties and protect the company's image. The Regulatory Affairs Analyst should be prepared to work in this environment and deliver the expected results through teamwork, timely and quality.

  • 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

Skills, Competencies and Knowledge

  • Ability to develop new projects, contingency plans and solution / mitigation of regulatory problems

  • Knowledge of the regulations applicable to new and biological drugs

  • Knowledge of Clinical Research regulations will be considered a differential

  • Ability to interact in all functions and geographies

  • Teamwork, interpersonal relationships, commitment and dynamism

  • Ability to communicate fluently (written and verbally) in English and Portuguese

  • Ability to organize / prioritize tasks

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.