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Regulatory Affairs Analyst (Hybrid)

Stryker
Full time
há 3 semanas
Work Flexibility: Hybrid

What You Will Do

We are seeking a Regulatory Affairs Analyst responsible for preparing and maintaining regulatory documentation for the registration and compliance of medical devices with ANVISA. This professional will manage product licenses, support new product launches, oversee electromedical certifications, and ensure all internal regulatory controls are up to date. The role requires strong collaboration with manufacturing sites, certification bodies, and internal teams, as well as a solid understanding of Brazilian regulatory frameworks. The ideal candidate will be highly organized, analytical, and capable of communicating effectively with external authorities and internal stakeholders.

Key Responsibilities:

What you need:

Required:

Preferred:

Travel Percentage: None

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