




Job Summary: Quality Assurance Assistant to support control and maintenance of the Quality Management System at a market-leading multinational. Key Highlights: 1. Supporting Quality Assurance activities in an industrial company 2. Monitoring and handling security and compliance information 3. Opportunity at a market-leading company with 47 years of experience We are the largest silicone implant manufacturer in Latin America, operating for 47 years and leading sales in Brazil. Founded in Rio de Janeiro in 1978, Silimed emerged from the initiative of a group of young entrepreneurs and has grown into a multinational present across South America, Europe, and Asia. Our goal? To expand and establish presence 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 an analytical **Assistant**, interested in processes, to join the **Quality Assurance** team of an industrial company. **MISSION:** To support Quality Assurance activities, contributing to the control and maintenance of the Quality Management System, as well as to monitoring and handling information related to safety, performance, and compliance of medical devices after commercialization. **REQUIREMENTS:** * Completed or ongoing undergraduate degree in Pharmacy; Biomedical Engineering; Nursing; Biomedicine; or related fields; * Intermediate 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 Quality Assurance Coordination; * Contribute to drafting and updating technical reports and departmental indicators; * Support post\-market surveillance, ensuring compliance with applicable regulatory requirements and deadlines; * Participate in drafting, reviewing, and controlling Quality procedures and records; * Support execution of internal audits and follow-up on corrective and preventive action plans; * Ensure that activities under one's responsibility are performed in accordance with internal procedures, quality standards, and current regulations.


