RBTG is part of the RBT Group, which operates in the medical products sector with a focus on quality, innovation, and safety. Our mission is to contribute to people's health and well-being through reliable and high-performance solutions. We value committed, collaborative professionals who constantly pursue excellence. We are seeking a **Quality Analyst** to work at the manufacturing plant, ensuring product compliance with sanitary regulations (**RDC 665/2022 and ISO 13485**) and internal company procedures. We are looking for someone with an execution-oriented profile who ensures quality directly within manufacturing operations, enjoys being close to the production process, and works practically to guarantee **control, documentation, and traceability** of all steps impacting product quality. **Main Responsibilities** * **Conduct** quality inspections in process and on final products, verifying compliance with technical specifications, work instructions, and production orders; * **Record and control** inspection results, segregating and identifying non-conforming products according to internal procedures; * **Execute and record** line releases, ensuring only conforming products proceed to subsequent stages; * **Maintain control and traceability** of batches, production records, and release reports, ensuring complete documentation; * **Perform non-conformity analyses and lead corrective and preventive action processes (NC, CA, and PA)** with relevant departments, ensuring effectiveness of actions; * **Work closely with Production, Logistics, Engineering, Maintenance, RT, and Procurement**, ensuring alignment and fulfillment of quality requirements; * **Participate technically in qualification of suppliers and service providers** applicable to production areas (calibration, maintenance, pest control, etc.); * **Maintain control and perform calibrations** of measurement instruments and equipment used in production, according to established schedules; * **Execute and monitor preventive maintenance** of production equipment and **oversee technical qualifications** performed by qualified suppliers; * **Conduct sampling and record results** of validation processes with suppliers and according to schedule; * **Prepare and support consolidation** of technical reports related to validation, calibration, and qualification; * **Ensure application of Good Manufacturing Practices (GMP)** across all production process stages, acting as technical compliance reference; * **Conduct operational and SGQ process training**, ensuring all personnel understand and apply Good Practices and internal procedures; * **Review, maintain, and update** quality documents (work instructions, procedures, manuals, and record forms); * **Control validity** of SGQ documents and certifications, supplier and customer certifications, requesting renewals when necessary; * **Conduct and support internal audits, certifications, and sanitary inspections**, providing required evidence and records; * **Investigate customer complaints and conduct technovigilance processes**, in partnership with the Specialist and Technical Responsible; * **Actively contribute to continuous process improvement**, aiming to reduce rework, increase productivity, and strengthen regulatory compliance; * **Execute and keep operational records updated** via computerized systems (Viman / VS Pratics), ensuring traceability and data integrity.