Pharmaceutical laboratory is seeking a Technician, Technologist, Professional, or student in fields such as Industrial Engineering, Chemistry, Pharmaceutical Chemistry, or related disciplines for the position of VALIDATION ANALYST. Working hours from Monday to Friday. Key responsibilities include: * Carry out, document, and follow up on activities related to process validations, cleaning procedures, equipment qualifications, analytical method validations, critical support systems, computerized systems, and spreadsheets. * Develop and execute qualification and validation protocols included in the validation master plan. * Prepare protocols and reports for equipment, process, system, and analytical technique qualifications and validations. * Organize and plan daily work with necessary resources according to the validation master plan. * Develop and review analytical procedures. * Participate in internal and external quality audit teams. * Actively contribute to data collection and analysis within the framework of the "Annual Product Review" system to evaluate trends in product parameters or variables. * Attend validation committee meetings to address relevant topics. * Collaborate with personnel from production, maintenance, quality control, and technical management to perform job functions. * Monitor calibration of instruments used in process qualification and validation. * Participate in process standardization. Other duties inherent to the position. Job type: Full-time