Gerente Pl Assuntos Regulatórios

Manage the regulatory portfolio for Oncology in Brazil, developing and executing strategies for initial registrations, new indications, line extensions, and lifecycle maintenance of medications. Lead submissions for new drug registrations and ensure compliance with ANVISA requirements. Conduct strategic interactions with ANVISA and evaluate opportunities to accelerate approvals for patient treatments.

Bachelor's degree in Pharmacy or related health sciences with relevant regulatory experience. Minimum of 7 years in Regulatory Affairs within the pharmaceutical industry, with strong knowledge of Brazilian regulations. Advanced or fluent English is required; Spanish is desirable but not mandatory.