**Date:** Nov 27, 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 mark on the world! **Type of collaborator** Trust **Position objective** Develop and modify monographs and inspection plans according to the demands from requesters across various service areas, as well as update monographs based on the latest edition of the applicable pharmacopeia(s). **Responsibilities and activities** * Carry out activities related to the Quality System under a compliance code with GMP. * Develop and update monographs and inspection methods according to established procedures and in compliance with current regulations. * Develop and update inspection plans and maintenance plans according to established procedures and in compliance with current regulations. * Create and update data in the system (Stability Module) according to established procedures and in compliance with current regulations. Experience 1 year in document control management Knowledge of regulatory compendia such as FEUM, USP (Not mandatory) Knowledge Laboratory process analysis GLP, GPP, GMP (Not mandatory) Education Bachelor's degree **Complementary Profile** Service attitude Adherence to standards Process control 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