Job Description and Details of Activities **Position Summary** The Quality Engineer role ensures that manufacturing processes comply with specifications and governmental standards. This role works to identify root causes and implement corrective actions in collaboration with various functional teams. It supports the change process related to raw materials. Essential Duties and Responsibilities The duties and responsibilities listed in this document are illustrative rather than exhaustive; therefore, the incumbent may perform other functions and tasks related to their area of work as derived from departmental objectives and strategies. * Be responsible for supervising quality systems in accordance with: * ISO 13485 requirements * CFDA requirements * Corporate policies and procedures * Other applicable national and international regulations/standards. Experience and Requirements **Knowledge and Skills** * Knowledge of quality systems required under ISO/GMP * Strong communication skills and sound logical thinking. * Integrity, ethical values, and attention to detail. Minimum Qualifications, Education, and Experience * Bachelor’s degree * 1–3 years of direct experience in the medical device industry or industries with similar regulatory requirements involving quality systems. (Educational requirements may be fulfilled through an educational institution or through equivalent work experience.) Benefits * Benefits as stipulated by the Federal Labor Law (LFT) * Life insurance * Savings fund * Medical expense insurance * Transportation * Inflation-adjustment plan * Guaranteed profit-sharing * Savings box * On-site medical services * Cafeteria * Life insurance * Annual bonuses * Savings fund * Cafeteria **Number of Vacancies** 3 **Department** Quality **Employment Type** Permanent **Work Modality** On-site **Shift** Day shift **Work Schedule** Full-time **Working Hours** Full-time **Education** Bachelor’s degree with professional title **English** Spoken: Intermediate, Written: Intermediate **Willingness to Travel** Yes