I am a Biomedical Doctor with 05 years of experience in Regulatory Affairs and Quality Assurance for medical device companies.
I work in Post Marketing Surveillance (PMS) and have experience in investigating technical complaints, adverse events, clinical evaluation and risk management according to regulatory requirements (ISO 13485, 14971, 20416 and RDC 665).
I also have skills with data analysis and visualization with tools (Ms PowerBI | Ms Excel | Power Query | ETL.