Job Summary: This position aims to identify, propose, and follow up on improvement opportunities in manufacturing processes to optimize efficiency and quality. Key Highlights: 1. Improvement of efficiency and quality in manufacturing 2. Establishment of preventive measures against recurrence 3. Analysis of improvement opportunities in manufacturing processes **Date:** Feb. 11, 2026 **Address:** TLAJOMULCO DE ZUÑIGA, JALISCO, MX **Company:** Grupo PiSA **Type of Collaborator** Trust-based **Job Objective** Identify, propose, and follow up on improvement opportunities in Electrolit’s manufacturing process stages to enhance efficiency and quality in production areas and establish measures to prevent recurrence. **Responsibilities and Activities** * Conduct activities associated with the Quality System under the GMP compliance code. * Timely communicate adverse events and quality issues detected through assigned activities to the Quality Unit. * Responsible for maintaining the integrity of information and data generated throughout the entire documentary chain related to their functions. * Analyze improvement opportunities identified during manufacturing processes and follow up on implementation. * Establish corrective measures for technical process problems and communicate root causes to personnel. Experience 1 year of experience in manufacturing processes within the pharmaceutical and/or food industry. Knowledge * Good Manufacturing Practices (GMP). * Knowledge of risk analysis tools for processes. * Proficiency in Microsoft Office software. Education Bachelor’s degree in Chemical-Pharmaceutical or Chemical-Biological fields