**Date:** Oct 9, 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!**Type of collaborator** Trust staff**Position objective** Ensure the correct documentation process of manufacturing files in order to achieve timely product release, as well as detect and follow up on deviations arising within the involved areas of Grupo PiSA.**Responsibilities and activities** Conduct activities related to the Quality System under a compliance code with GMP. Analyze and identify process deviations generated during manufacturing. Document and manage corrective and preventive actions (CAPA), as well as oversee change controls generated in the manufacturing areas. Manage changes in documentation (Master Batch Record MBR and Standard Operating Procedures SOP). Review and approve master manufacturing records. Manage the closure of documentation for manufactured batches. Experience Experience handling file closures. Education Bachelor's degree in Chemical Engineering or \*Related fields At Grupo PiSA, we prohibit violence and discrimination, promoting equal opportunities, inclusion, and diversity. Our selection processes are FREE of charge; report any irregularity at lineaeticagrupopisa@letica.email