Assist in accompanying the Regulatory Affairs plan of the sector, managing the medical product registration plan with ANMAT and ENACOM
Job Summary
Assist in accompanying the Regulatory Affairs plan of the sector, managing the medical product registration plan with ANMAT and ENACOM.
Coordinate and manage regulatory documents with international suppliers, and manage and analyze claim indicators (KPI) for service improvement.
Collaborate in the preparation of safety campaigns to foster a culture of care and assist in the preliminary identification of risks in O2 and ventilation.
Matching Summary
Assist in accompanying the Regulatory Affairs plan of the sector, managing the medical product registration plan with ANMAT and ENACOM.
Skills & Requirements
Must-have
ANMAT and ENACOM registrations
international regulatory documents
Tecnovigilancia documentation management
claim indicators analysis
O2 and ventilation risk identification
medical equipment forms validation
Nice-to-have
fostering solid relationships
continuous improvement
team development facilitation
safety culture promotion
detailed technical vision
Key Requirements
Advanced student of Bioengineering or Biomedical Engineering