Responsible for collecting documentation and implementing the Quality Management System for medical devices according to the ISO 13485:2016 standard, from the creation of the processes, establishment of their measurement parameters and compliance with legal requirements, such as decree 4725 of 2005 and resolution 4816 of 2008. In conjunction with the SG-SST administration.

Structure, develop and finalize research project for a new product line for launch in 2023 focused on Medical Devices.

Responsible for ensuring that the custom PEEK, PMMA and Titanium implants met the organization's requirements with documentary support, I was also in charge of meeting the requirements requested for the failure analysis of osteosynthesis materials and providing support to the commercial area with all the requirements they had with maxillofacial specialists, neurosurgeons, orthopedists and chest doctors.

Make a methodological proposal for the development of a Medical Device, advise on the purchase of equipment and structuring procedures for the operation of FCP.

Responsible for carrying out the optimization and standardization of the pigment weighing process for the manufacture of tires, according to the recipes requested by the compounder and programming orders requested by the operational process, along with the QMS audit for compliance with the requirements. of the ISO 9001:2015 standard, and support in second-party external audits and recertification. The administration of the SG-SST is also carried out.

Completion of a 50-hr ARL course and morphological characterization of raw materials for machine design and development with international suppliers.