Estágio em Assuntos Regulatórios, 2026

Prepare technical documentation for new product registration, renewals, and post-registration changes in Brazil, ensuring compliance with ANVISA regulations and internal procedures. Monitor daily regulatory intelligence from ANVISA and competitor sites based on assigned intellectual property. Support change control processes by managing the lifecycle of change requests, including initiation, closure, and follow-up. Organize and route internal documents for official dispatch to regulatory authorities. Collaborate on strategic discussions regarding synthetic and biologic products while assisting in Good Manufacturing Practice certifications across multiple manufacturing sites.