Sr Manager, Regulatory Affairs

Gilead Sciences

Sao Paulo, Brazil
On-site
Local regulatory strategies
Strategic and tactical regulatory advice
Regulatory interface with anvisa
Gilead Sciences is seeking a Senior Manager of Regulatory Affairs in São Paulo, Brazil, to lead local regulatory strategies for their products and pipeline assets. The ideal candidate will have extensive experience in regulatory affairs, particularly within the Brazilian market, and will play a critical role in ensuring compliance and successful interactions with health authorities

Job Summary

  • Lead and own the development, execution and oversight of local regulatory strategies for registered products and pipeline assets, ensuring alignment with global and regional regulatory objectives.
  • Serve as a regulatory interface with ANVISA and other relevant external stakeholders, leading health authority interactions, negotiations and regulatory discussions, in alignment with Gilead policies and standards.
  • Provide regulatory intelligence and thought leadership, contributing to internal discussions, trade associations and public consultations, supporting the shaping and implementation of regulatory requirements in Brazil.

Matching Summary

Match Score: 85

Gilead Sciences is seeking a Senior Manager of Regulatory Affairs in São Paulo, Brazil, to lead local regulatory strategies for their products and pipeline assets. The ideal candidate will have extensive experience in regulatory affairs, particularly within the Brazilian market, and will play a critical role in ensuring compliance and successful interactions with health authorities.

Skills & Requirements

Must-have

  • local regulatory strategies
  • strategic and tactical regulatory advice
  • regulatory interface with ANVISA
  • monitor regulatory environment changes
  • regulatory risk assessments
  • promotional and non-promotional materials review

Nice-to-have

  • sense of urgency and priorities
  • agile in an evolving environment
  • resilient with ability to influence
  • demonstrate leadership commitments
  • contribute to continuous improvement

Key Requirements

  • Bachelor’s degree in Pharmacy / Biochemistry
  • 8–10 years of progressive regulatory affairs experience
  • Strong exposure to Brazilian regulatory requirements
  • Fluency in English is required

Work Rights

Not specified

Tailored Resume

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