Summary: This role involves establishing and monitoring quality standards, managing documentation, conducting audits, identifying and resolving non-conformities, and proposing improvements within a laboratory setting. Highlights: 1. Establish and monitor quality standards (ISO 17025, GLP) 2. Manage quality-related documentation and conduct audits 3. Identify non-conformities, propose improvements, and train employees Curitiba, Brazil Laboratory Job Type: Full Time Main Activities: * Establish and monitor quality standards: Define metrics and criteria to evaluate quality, ensuring that services and processes comply with the standards established by ISO 17025 and GLP; * Manage documents: Organize and maintain quality\-related documentation, such as manuals, procedures, and work instructions. * Conduct/organize/monitor internal (ISO 17025\) and external (CGCRE/INMETRO) audits. * Identify and resolve non\-conformities: Detect deviations from quality standards and propose corrective actions to ensure compliance. * Propose improvements: Identify opportunities for improvement in processes, products, and services, suggesting new technologies, methods, or processes to increase efficiency and quality. * Evaluate suppliers: Analyze supplier performance in relation to established quality standards, ensuring that the materials and services received meet the requirements. * Train employees: Train employees on quality standards and procedures, promoting awareness and engagement with the quality culture. Required Qualifications: * Academic Background / Courses: Completed Higher Education or Technical Course. * 2 years of experience in Quality Management focusing on ISO 17025\.
João Silva
Indeed · HR
João Silva
Indeed · HR
