- Drive organizational change by championing process improvement initiatives and fostering a culture of continuous improvement, promoting best practices and accountability. - Organize and lead global and cross-functional teams. - Facilitate workshops, Value Stream Mapping, and project meetings.- Identify and mitigate project risks. Define and respect project roadmaps. - Communicate process changes and updates to stakeholders and provide support throughout the transition period.- Lead change management activities.- Identify, obtain and maintain executive sponsorship- Prepare and present progress reports, highlighting key findings, trends, and recommendations to senior management and project sponsors.- Author process documentation: procedures, work instructions, guides, and diagrams.- Analyze Business Intelligence (BI) data and create visual reports to communicate performance.- Build and roll-out a training plan for engineers

- Identify product requirements based on internal and external stakeholders' needs.- Electro-mechanical design and development.- Perform Design and Process Failure Mode and Effects Analysis (DFMEA and PFMEA).- Lead product verification and certification activities, including tests performed by Nationally Recognized Testing Laboratories (NRTL) (IEC 60601-1 and IEC 60601-1-2).- Biocompatibility evaluation, testing, and risk analysis (ISO 10993-1, 10993-5, and 10993-10)- Collaborate with cross-functional internal and external teams in different countries to ensure product compatibility.- Support for ISO13485, MDSAP, INMETRO, and MDR audits

Medical device product development (R&D), Manufacturing Engineering, and Engineering changes:- Project management for engineering changes and PLM Key user (Enovia).- Technical problems solving- Electromechanical and Computer-assisted design (CAD)- Supplier selection, qualification, and integration. - Production transfer, including implementing incoming quality controls, training of manufacturing employees, and First article inspections.- Support QA team for ISO13485, MDSAP, INMETRO, and MDR audits.- Requirements definition from internal and external stakeholders.

Design, optimization, and verification of a patient positioning medical device:- Computer-assisted design (SolidWorks)- Redaction and execution of verification protocols and reportsImplementation of a new electronic system for Product lifecycle management (PLM):- Project Management- Data processing- Process reengineering- Employee training

Design of a standardized template for the processing and registration of PET brain images:- Positron emission tomography (PET) image processing - Creation of a standardized template to facilitate PET image processing- Matlab, linux, and shell programming