Description and details of activities * Intermediate to advanced English (spoken and written). * Collaborative leadership with a technical focus on continuous improvement, product safety, and regulatory compliance. * Ability to present, justify, request support at different organizational levels, and generate executive reports for senior management. * Accuracy and attention to detail in data analysis and preparation of technical documentation. * Skill in coordinating actions with multidisciplinary teams, without direct personnel responsibility. * Self-management, critical thinking, and decision-making. * Project management and administration with a results-oriented approach. * Maintain effective communication with support groups and sister plants. Experience and requirements * University degree in Engineering or related field. * Minimum of 3 years of professional experience in technical or regulated areas, focused on analysis, continuous improvement, or regulatory compliance. * Solid knowledge of manufacturing processes and quality management systems. * Experience in statistical analysis and problem-solving methodologies. * Advanced proficiency in databases and analysis tools. * Familiarity with regulations applicable to medical devices (FDA, ISO 13485, MDSAP, etc.). * Proficiency in computer tools: Microsoft Office; preferably Oracle, TrackWise and Agile. Benefits * Life insurance * Savings fund * Medical expense insurance * Transportation * Daycare * Guaranteed bonuses * Savings box * On-site medical services * Dining room * life insurance * Benefits according to the Federal Labor Law **Number of vacancies** 1 **Area** Quality **Contract** Permanent **Modality** In-person **Shift** Daytime **Workload** Full-time **Schedule*** Full-time **Education** Professional degree **English** Spoken: Advanced, Written: Advanced **Travel availability** No