




Job Summary: Quality Assurance Assistant to work in an industrial company, providing analytical support for controlling and maintaining the Quality Management System. Key Highlights: 1. Support for Quality Assurance activities 2. Monitoring and handling of medical device safety information 3. Support for technical investigations and report preparation We are the largest silicone implant manufacturer in Latin America, operating for 47 years and market leaders in sales across Brazil. Founded in Rio de Janeiro in 1978, Silimed originated from a group of young entrepreneurs and today is a multinational with presence in South America, Europe, and Asia. Our goal? To expand and be present on every continent. We are relentless in pursuing victory, proud of our journey, and passionate about what we do. Our culture and values have sustained Silimed at the top for over 47 years. We believe in developing people and driving successful careers. We seek a **Quality Assurance Assistant** with an analytical profile and interest in processes to join the **Quality Assurance** team of an industrial company. **MISSION:** Provide support to Quality Assurance activities, contributing to the control and maintenance of the Quality Management System, as well as to the monitoring and handling of information related to the safety, performance, and conformity of medical devices after their commercialization. **REQUIREMENTS:** * Completed or ongoing undergraduate degree in Pharmacy; Biomedical Engineering; Nursing; Biomedicine; or related fields; * Intermediate-level Office software proficiency; **PREFERRED:** * Experience in processes relevant to the Quality Assurance area. **SOFT SKILLS:** * Organization and attention to detail; * Strong written and verbal communication skills; * Collaboration and teamwork; * Commitment to deadlines. **RESPONSIBILITIES:** * Support monitoring and recording of adverse events and technical complaints related to medical devices; * Assist in collecting, organizing, and performing preliminary analysis of data from internal and external notifications; * Support technical investigations under guidance from the Technovigilance Analyst or the Quality Assurance Coordination; * Contribute to preparing and updating technical reports and departmental indicators; * Support post\-market surveillance, ensuring compliance with applicable regulatory deadlines and requirements; * Participate in developing, reviewing, and controlling Quality procedures and records; * Support conducting internal audits and tracking corrective and preventive action plans; * Ensure that activities under one's responsibility are performed in accordance with internal procedures, quality standards, and current regulations.


