• Deviation Management, with initial assessment and final approval, along with support for the entire production plant;• Complaints Management, with initial assessment and final approval, as well as reporting to the Client;• CAPA Management, opening and final approval;• Risk Management;• Production Support - Environmental Monitoring;• Assessment of the Effectiveness of action plans implemented for Deviations, Complaints and OOS;• Impact Assessment and Risk Analysis for Quality Change and Quality Event;• Execution and Reporting of Operations Quality Indicators;• Deviation and CAPA Trend Analysis;• Internal Audit and support in External Audits (Regulatory and Supplier);• Anual Periodic Review Deviations and CAPAs;• Review and Approval of Standard Operating Procedures;• FMEA Production Lines;• Production Support, oversight and assistance in investigating nonconformities; • Customer QA Support.

• Focal point in conducting laboratory events (OOS and OOL), for opening and conducting laboratory investigations;• Focal point in investigating and assessing quality deviations (nonconformities), managing the implementation and compliance with CAPA actions;• Development of projects focused on quality;• Reporting of plant quality indicators (KQI);• Support in internal and external audits (Corporate Audits, ANVISA);• Support in managing training and integration of new employees;• Preparation and review of operational procedures;• Support in developing, communicating and implementing quality strategies in line with the objectives of management and the global team.

• Analyzes of raw materials according to methodologies regulated by USP, Brazilian Pharmacopoeia and European Pharmacopoeia;• Physicochemical analyzes for release of raw materials, in-process control and finished product;• Physicochemical analyzes of WFI and purified water;• Routine execution in the laboratory for calibration and preventive maintenance of equipment, and preparation and factoring of solutions;• Qualitative and quantitative analyzes using techniques such as: Chromatography (TLC, HPLC), Spectrophotometry (UV/Visible, IR and Atomic Absorption), Titrimetry (Tituprocessor);• Operation of analyzes with the following equipment: Particle Counter, Osmometer; Colorimeter, Polarimeter and Flame Photometer;• Software: Empower 3, POMS, TCU, Lims and TrackWise 8; • Critical evaluation of analytical results versus specified limits, verifying the existence of laboratory events (OOS and OOL), as well as opening and conducting laboratory investigations;• Investigation and evaluation of quality deviations (non-conformities), managing the implementation and compliance with actions for their correction (CAPA).

• Preparation of Technical Data Sheets and Chemical Product Safety Data Sheets (MSDS);• Preparation of reports and monitoring of water potability analyses – Ordinance No. 2,914 of the Ministry of Health;• Performing analyses and monitoring of the chemical treatment of industrial water (chilled water, boiler and cooling tower);• Optimizing the preparation of technical reports on drinking and industrial water, reducing the delivery time to the customer by 48 hours;• Service, support and clarification to an average of 30 customers per week, improving response time by 60% and customer satisfaction by 90%;• Operation, organization and cleaning of the laboratory and raw materials in accordance with Good Laboratory Practices;• Preparation of maps of controlled chemical products for the Federal Police and Army;• Preparation and review of the laboratory's technical documentation;• Performing analyses of products for the treatment of drinking and industrial water;• Assistance in the operation of the Pilot Water Treatment Plant.

• Preparation of the Good Manufacturing Practices Manual (GMP) and SOPs;• Coordination of the entire process of granting the Company Operating Authorization (AFE) with ANVISA;• Monitoring and supervision of the production line for process validation and cleaning;• Implementation of a continuous improvement program for production planning and control;• Mapping of data for adaptation and development of production processes;• Quality control of raw materials and finished products;• Reduction of inventory costs and product losses, after the start of monthly inventory audits;• Qualification of suppliers, preliminary cost survey and purchase of raw materials;• Review of the product pricing strategy, resulting in growth of up to 50% in the profit of certain products;• Planning of delivery routes and sales logistics;• Preparation of product profit margin reports;• Review of mandatory nutritional labeling according to ANVISA standards.

• Participation in a multidisciplinary technical team of the Repository Project for Low and Medium Level Radioactive Waste – RBMN;• Creation of a partnership with the Department of Transportation Engineering and Geotechnics of the UFMG School of Engineering;• Bibliographic survey;• Planning and execution of experiments for soil and bentonite characterization;• Operation, analysis and interpretation of the results of characterization tests – X-ray Diffraction, Scanning Electron Microscopy (image and EDS), Granulometric Distribution, Moisture Content, Specific Surface, Particle Density, Cation Exchange Capacity and Hydraulic Conductivity;• Training, support and technical assistance to IC students;• Production of technical reports, scientific articles and presentation of papers at conferences.

• Receiving raw materials, checking the order against the invoice, ensuring compliance with the specifications reported by the suppliers;• Quality control: visual and temperature control of the finished product, control of the temperature of the cooling chamber, pH control of the supply water; control of shelf-life and check-lists;• Development of a project to test product recipes to investigate non-conformities: quantitative and qualitative tests of the ingredients used in the product recipes, with the aim of improving the finished product and increasing shelf life;• Production scheduling according to orders forwarded by the sales department;• Monitoring the production line and mapping the processes to identify the root cause and propose ways to prevent recurrence of product quality deviations;• Review and update of the GMP.