As a Senior Researcher, I lead various initiatives at the analytical research and development laboratory for cosmetics. In addition to conducting precise benchtop analyses, I oversee accelerated and long-term stability studies to ensure product quality and durability. I develop and implement advanced analytical methods to optimize processes in the factory, providing technical support and ongoing training for the technical team. I manage the calibration, qualification, and maintenance of all equipment, ensuring compliance and operational efficiency.My responsibilities include strategic team activity allocation, procurement of reagents, negotiation of contracts with commercial partners, and laboratory management. I am directly involved in managing critical projects for new product and method development not only in Brazil but across Latin America. Additionally, I organize events, conduct training sessions, and oversee the writing and review of technical documents. I perform literature research, respond to audits from regulatory and law enforcement agencies, conduct statistical analyses, and create BI dashboards to support strategic decision-making.

As a Quality Control Analyst, I played a pivotal role in managing and executing various additional responsibilities. In addition to overseeing finished product analysis, process validation, product stability, and SOP creation, I was responsible for the transfer of analytical methodology between company sites, ensuring compliance with current legislation, particularly RDC 166. I conducted technical training for technicians, assistants, and junior analysts, ensuring uniformity and high standards in analytical operations. As the technical focal point, I responded to regulatory demands from ANVISA during regulatory inspections, as well as other agencies such as the Civil Police, Federal Police, and Army, demonstrating my commitment to regulatory compliance and operational excellence.

As a Quality Control Analyst, I had a diverse and strategic role. In addition to overseeing finished product analysis, process validation, and water validation, I handled analysis of market complaint products and imported products. I made significant contributions to product stability, conducting analyses, documenting long-term stability reports, and performing statistical analyses of stability data. I ensured the accuracy of calculations and technical documentation prior to the release of finished products. I played a pivotal role in technical investigation processes related to analyses or products and was responsible for creating and revising Standard Operating Procedures (SOPs). Additionally, I actively trained junior analysts, sharing knowledge and best practices.

I have extensive experience as the focal point for finished product analysis, process validation, and water validation in the pharmaceutical industry. I utilized advanced techniques such as HPLC, GC, and Dissolution to ensure product compliance with regulatory standards. One of my major accomplishments was leading and implementing the 5S project in the Quality Control laboratory, resulting in significant improvements in workplace organization and efficiency. Additionally, I was responsible for creating and implementing the 5S documents. I contributed to the preparation of validation reports and actively participated in continuous improvement projects aimed at optimizing processes and ensuring the quality of pharmaceutical products.

I worked as a Junior Quality Control Analyst specializing in the analysis and characterization of raw materials. My role involved receiving, analyzing, and characterizing raw material samples using techniques such as infrared spectroscopy. I conducted a variety of physical-chemical to ensure that raw materials met required quality specifications. Additionally, I played a critical role in releasing raw materials for pharmaceutical production, utilizing systems like SAP and LIMS to manage documents and processes, ensuring efficiency and accuracy. I also reviewed and verified technical documentation, including release certificates and standard operating procedures (SOPs), ensuring regulatory compliance and product quality. I collaborated closely with multidisciplinary teams to achieve consistent and effective outcomes.

Responsible for receiving and analyzing samples of process control, finished product, semi-finished product, and raw materials in the Quality Control laboratory. Conducted a wide range of tests to ensure compliance with quality specifications. Additionally, played a crucial role in releasing raw materials for pharmaceutical production, ensuring compliance before production commencement.Utilized SAP and LIMS tools to manage documents and processes, ensuring efficiency and accuracy. Also reviewed and verified technical documentation, including release certificates and standard operating procedures (SOPs), ensuring regulatory compliance and product quality. Worked closely with multidisciplinary teams to achieve consistent and effective outcomes.

As a Chemist in the Research and Development Laboratory, I conducted detailed physico-chemical analyses of raw materials and pilot batches of products under development, ensuring compliance with technical specifications. I specialized in stability analysis using methods such as Conductivity and pH MRC. Additionally, I led the calibration (RBC) of essential equipment including pH meters, conductivity meters, thermometers, and fluoride-selective electrodes, ensuring accuracy of results. I managed quality control documentation in accordance with current legislation, including standards such as ABNT NBR ISO 17025, ABNT NBR ISO GUIDES 30 and 31, ensuring compliance and efficiency in laboratory processes.