The role is responsible for ensuring portfolio compliance with ANVISA by leading registration, renewal, and post-registration change processes
Job Summary
The role is responsible for ensuring portfolio compliance with ANVISA by leading registration, renewal, and post-registration change processes.
Candidates will collaborate with Quality, Pharmacovigilance, Operations, and the Campinas factory to align regulatory documentation with production processes.
The position offers exposure to a robust portfolio of generics and similar medicines within a dynamic regulatory team focused on patient access.
Matching Summary
The role is responsible for ensuring portfolio compliance with ANVISA by leading registration, renewal, and post-registration change processes.
Skills & Requirements
Must-have
Knowledge of Brazilian sanitary legislation
Experience with ANVISA registration processes
Ability to manage regulatory lifecycle
Nice-to-have
Competitive intelligence in pharma market
Collaborative teamwork skills
Proactive problem solving approach
Key Requirements
Degree in Pharmacy, Biochemistry, or Chemistry
Intermediate or advanced English proficiency
Desirable experience in pharmaceutical industry regulatory affairs