Active participation in Validation processes of Laboratory systems, including densimeters and monitoring systems, between essential equipment.Effective collaboration between in multidisciplinary teams, guaranteeing the integration and effectiveness of the validation projects. Specialization in Computer Systems Validation and electronic records, in accordance with GxP, GAMP 5 and ALCOA+.Soid experience in equipment and systems validation related to clinical analysis laboratory and the pharmaceutical industry.Proficiency in data collection and analysis, which are fundamental to base validation processes and decision making.Establishment of solid and efficient relationships with clients, acting as the main interface to guarantee the satisfaction and understanding of needs.Development and implementation of personalized strategies to solve the clients problems in an efficient manner.Meticulous preparation of technical documentation and performance reports, in accordance with current legislation and international standards.Proficiency in the Office package to carry out administrative tasks and prepare reports.Experience in project management, ensuring deadlines and quality of deliveries are met.Ability to prepare technical documentation in accordance with standards established by ANVISA, FDA and other relevant regulations.