SENIOR RESEARCH AND DEVELOPMENT ANALYST

Description

Job Summary: Senior Research and Development Analyst responsible for executing development and improvement projects for implantable medical devices, with a focus on silicone prostheses. Key Highlights: 1. Leader in silicone implants in Latin America 2. Focus on safety and compliance with national and international standards 3. Opportunity for technical mentoring and continuous process improvement We are seeking a Research and Development Analyst to join our team! We are the largest silicone implant manufacturer in Latin America, with 45 years in the market and market leader in sales in Brazil. Founded in Rio de Janeiro in 1978, Silimed emerged from the initiative of a group of young entrepreneurs and has today become a multinational company present in South America, Europe, and Asia. Our goal? To expand and be present on all continents. We are driven to win, proud of our journey, and passionate about what we do. Our culture and values have sustained Silimed at the top for over 40 years. We believe in developing people and advancing successful careers. Responsible for executing new product development and improvement projects for implantable medical devices, with a focus on silicone prostheses, ensuring safety and compliance with national and international standards. Key Responsibilities: * Prepare project documentation. * Execute development of new products and improvements to existing products, in accordance with procedures. * Prepare and review technical drawings and product specifications. * Analyze reports from mechanical and performance tests, in accordance with ISO 14607 and RDC 848:2024\. * Prepare test and shelf-life study reports. * Collaborate with regulatory affairs, quality, production, PCP, and marketing departments to ensure technical alignment of deliverables. * Monitor pilot manufacturing processes. * Use PPEs. * Participate in technical audits and provide technical support for national and international certifications (e.g., CE Mark, FDA). * Serve as technical mentor to junior analysts and contribute to continuous improvement of R&D processes. **Technical Requirements:** * Bachelor's degree completed in Pharmacy, Chemistry, Biomedicine, Physical Therapy, Biology, or Toxicology. * Minimum 3 years of experience in the field. * Preferred: Experience in planning and managing medical device development projects. * Familiarity with applicable technical standards (e.g., ISO 10993, ISO 13485, RDC 751/2022, MDR 2017/745\). * Intermediate technical English.