Especialista Asuntos regulatorios Licitaciones

Responsible for managing planning of medical device registration projects in Mexico and LATAM, including budgeting, preparing and submitting dossiers to the Ministry of Health (COFEPRIS), and obtaining approvals for new registrations, renewals, modifications, import permits, advertising notices, technovigilance reports, and NOM 137 labeling. The role maintains awareness of regulatory changes affecting medical devices and coordinates with manufacturers, distributors, and internal commercial, marketing and supply chain teams to support product launches.