Analista de Farmacovigilância Pl (vaga afirmativa para pessoas pretas e pardas)

Prepare regulatory submissions, manage adverse event reports, and oversee risk management plans for pharmaceutical products. Draft and maintain standard operating procedures, training materials, and regulatory documents while interacting with global matrices and partners. Support audit readiness, third-party approvals, and CAPA action plans within the pharmacovigilance department. Monitor regulatory updates and assist in translating product labeling. Act as a backup for case processing and operational activities. Requires pharmacy degree, advanced English, and relevant experience. Full-time role in Brazil with salary commensurate with experience.