**Date:** Oct 22, 2025 **Address:** Carr. a San Isidro Mazatepec 7, JALISCO, MX **Company:** Grupo PiSA Live your purpose and make a difference with Grupo PiSA. With over 80 years of history, Grupo PiSA is a 100% Mexican company committed to the health and well-being of millions of people, both in Mexico and internationally. Our growth reflects the effort, passion, and dedication of a team focused on excellence. Join us and become part of a company where every day is an opportunity to live "A Life in Service of Life". Together we can transform the future of health and leave a positive impact on the world! **Position Objective** Manage, ensure, and guarantee the reliability and integrity of physicochemical analytical results involved in the assessment of raw materials, in-process products, and finished products, as well as in supporting analyses for qualification and/or validation of critical systems, deviation investigations, and complaints. **Responsibilities and Activities** * Lead activities related to the Quality System under a Good Manufacturing Practices (GMP) compliance code. * Manage laboratory-related activities in accordance with the quality system and regulatory compliance requirements before national and international authorities. * Define strategies and lead continuous improvement projects within the quality system to mitigate production risks and ensure regulatory compliance across all processes. Experience 5 or more years in: * Pharmaceutical industry. * Personnel management. * National and international health regulations. * Quality management systems. * Management of FQ and MB laboratories. Education * Master's degree desirable Bachelor's degree in Chemical-Pharmaceutical or Chemical-Biological fields At Grupo PiSA, we prohibit violence and discrimination, promoting equal opportunities, inclusion, and diversity. Our selection processes are FREE of charge; report any irregularities at lineaeticagrupopisa@letica.email