Staff Regulatory Affairs Specialist (Hybrid)

Stryker do Brazil Lda

📍 São Paulo, State of São Paulo, Brazil

Full time Business Operations Specialists Posted March 01, 2026

Job Description

Work Flexibility: Hybrid

What you will do

In this role, you will support the Neurovascular Division in Brazil, ensuring regulatory compliance for Class III and IV medical devices while collaborating within a LATAM matrix structure.

Main responsabilities:

  • Prepare, submit, and maintain regulatory submissions to ANVISA for Class III and IV medical devices, including monitoring authority reviews and managing follow-up actions.

  • Maintain product registrations and support new product launches in Brazil, ensuring compliance with applicable RDCs and local regulatory requirements.

  • Provide regulatory guidance on product lifecycle changes, including Change Notification assessments, impact analysis, filing strategy, and development of local regulatory action plans.

  • Ensure full adherence to the Brazilian Quality Management System and applicable regulatory procedures, in coordination with the local regulatory team.

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