Professional with solid experience in Quality Management Systems (QMS) in a regulated medical device company. Works independently in conducting critical activities in compliance with national and international regulations (ANVISA, ISO 13485, MDSAP, MDR, FDA), supporting the implementation and maintenance of quality systems. Participates in product development projects under Design Control, risk analysis, internal and external audits, and actively contributes to committees such as Change Control and MRB. Works in supplier management, CAPA control, continuous improvement support, and technical training...