Job Summary: A quality management professional responsible for implementing, maintaining, and auditing quality management systems to ensure regulatory compliance for products. Key Highlights: 1. Implementation and maintenance of QMS procedures in accordance with ISO 9001/ISO 13485 2. Conducting internal and external audits 3. Ensuring regulatory compliance with ANVISA, RDCs, and INMETRO Bachelor's degree in Quality Management, Biomedical Systems Technology, or Pharmacy. Responsibilities: Implement, maintain, and update QMS procedures in accordance with applicable standards (ISO 9001/ISO 13485). Conduct internal and external audits to verify compliance with regulatory requirements. Analyze nonconformities and implement corrective and preventive action plans, as well as related work instructions and forms. Ensure regulatory compliance of products and processes according to current legislation (ANVISA, RDCs, INMETRO). Collaborate with R&D, production, and marketing departments to ensure products comply with regulatory requirements from development through commercialization. Participate in regulatory audits (e.g., ANVISA, ISO) and provide technical support when required. Reside in Itu/Salto or Sorocaba/Indaiatuba. Employment Type: Full-time CLT Compensation: R$7,000.00 – R$8,000.00 per month Benefits: * Transportation allowance Work Location: On-site