Description: * Technical or higher education degree in Chemistry, Biology, Biomedicine, Pharmacy, Chemical Engineering, or related fields. * Knowledge of Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and Good Documentation Practices. * Prior experience in a quality control laboratory, performing physicochemical and/or microbiological analyses. * Perform physicochemical and/or microbiological laboratory analyses on raw materials, intermediate products, and finished products, in accordance with established methodologies, standards, and specifications. * Record, control, and verify analysis results in designated systems, ensuring data traceability and compliance with Good Documentation Practices. * Conduct inspections and verifications of production processes, ensuring adherence to the company’s defined quality standards. * Support investigations of non-conformities, process deviations, and quality complaints by providing necessary information, records, and analyses. * Assist in the preparation, review, and updating of quality documents, such as SOPs, work instructions, technical specifications, and forms. * Perform environmental and utilities monitoring routines according to internal schedules and regulatory requirements. * Support equipment qualification, cleaning validation, and process validation activities, as applicable. * Manage retention samples, standards, and reagents, ensuring laboratory organization, identification, and environmental integrity. * Contribute to continuous improvement initiatives by supporting the implementation of corrective and preventive actions. * Provide support to other departments within the company and guide less experienced professionals on matters related to the area of expertise. * Perform other related activities as directed by immediate leadership. 2512210202551931254