




Job Summary: This professional will support the analysis of regulations, development of procedures, extraction of data, and recording of adverse events in pharmacovigilance. Key Highlights: 1. Will support the analysis of pharmacovigilance resolutions and ordinances 2. Will assist in the development, review, and implementation of internal procedures 3. Will participate in audits and regulatory inspections Description: * Currently pursuing a bachelor's degree in Pharmaceutical Sciences, Biomedicine, or Nursing; * Intermediate English proficiency; * Intermediate proficiency in Microsoft Office suite; * Prior experience in pharmacovigilance or technical documentation within the pharmaceutical industry is desirable; * Willingness to travel occasionally; * Availability to work Monday through Friday, from 8:00 AM to 5:00 PM, in Itapira/SP. * Support the analysis of pharmacovigilance-related resolutions and ordinances; * Assist in the development, review, and implementation of internal procedures; * Extract data from the pharmacovigilance database and collaborate on drafting legal documents and internal reports; * Perform collection and registration of adverse events in the database, assessing causality when necessary; * Participate in activities related to internal/external audits and regulatory inspections. 2512100202181911602


