




Job Summary: This role supports pharmacovigilance activities, including analysis of regulations, development of procedures, data extraction, adverse event reporting, and participation in audits. Key Highlights: 1. Support in analyzing pharmacovigilance resolutions and ordinances 2. Assistance in drafting and reviewing internal procedures 3. Participation in internal/external 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 analysis of pharmacovigilance-related resolutions and ordinances; * Assist in drafting, reviewing, and implementing internal procedures; * Extract data from the pharmacovigilance database and support preparation of legal documents and internal reports; * Perform adverse event capture and registration in databases, assessing causality when necessary; * Participate in activities related to internal/external audits and regulatory inspections. 2512100202181911602


