Quality Control Analyst

Description

Job Summary: We are seeking a Mid-Level Quality Control Analyst to analyze and monitor production processes, ensuring compliance with quality standards and regulatory requirements. Key Highlights: 1. Conduct analysis and monitoring of production processes 2. Ensure compliance with quality standards 3. Focus on continuous improvement and regulatory assurance 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 emerged from the initiative of a group of young entrepreneurs and has since grown into a multinational company with presence across South America, Europe, and Asia. Our goal? To expand and establish presence on all continents. We are looking for a Mid-Level Quality Control Analyst to analyze and monitor production processes, ensuring compliance with quality standards and regulatory requirements. If you possess strong attention to detail, interest in this field, and the desire to grow with us, this position is for you! **What we expect from you:** * Intermediate/advanced English proficiency (desirable) * Intermediate knowledge of MS Office applications (Word, Excel, PowerPoint) * Minimum 3 years of experience in processes relevant to this area * Knowledge of continuous improvement tools (e.g., PDCA) * Basic knowledge of applicable standards (GMP, ISO 13485) * Experience with chromatography (HPLC and GC) * Experience with analytical method validation * Experience with rheology (desirable) **Responsibilities:** * Perform chemical and physicochemical analyses of raw materials, inputs, and finished products, following standard operating procedures (SOPs) and internal standards * Conduct tests using chromatographic techniques (HPLC and GC) and interpret the obtained results * Execute analytical method validations, ensuring compliance with criteria for precision, accuracy, and robustness * Record and document all results in systems or spreadsheets, ensuring data traceability and integrity * Support continuous improvement initiatives by applying tools such as PDCA to optimize laboratory routines * Assist in implementing and maintaining GMP and ISO 13485 standards, ensuring regulatory compliance * Perform rheological analyses when required, interpreting data and contributing to formulation adjustments * Collaborate with the team on product development projects and resolution of non-conformities * Participate in training and technical updates to continuously enhance laboratory competencies.