Job Summary: This position focuses on conducting and documenting validation and qualification studies for manufacturing processes, systems, equipment, and areas to comply with regulatory requirements and objectives. Key Highlights: 1. Part of a 100% Mexican company with an 80-year history. 2. Contributes to the health and well-being of millions of people. 3. Works within a team focused on excellence. **Date:** Feb. 6, 2026 **Location:** TLAJOMULCO DE ZUÑIGA, 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 healthcare and leave a positive impact on the world! **Employment Type** Confianza**Job Objective** Conduct and document applicable validation and qualification studies for manufacturing processes, critical systems, equipment, areas, facilities, and cleaning activities involved in pharmaceutical manufacturing to comply with current regulations and established objectives.**Responsibilities and Activities** 1. Perform activities associated with the Quality System under a code of compliance with Good Manufacturing Practices (GMPs). 2. Execute and monitor validation and qualification activities for assigned equipment and/or systems. 3. Conduct qualification and/or validation tests and perform corresponding analyses to generate conclusions regarding equipment and process operations in required reports. 4. Monitor deviations identified during execution of assigned qualifications or validations. 5. Support involved departments in implementing improvement projects for facilities, equipment, or processes (new or transferred). Experience * Pharmaceutical and/or food industry. * Equipment, process, area, and utility validation and qualification. Knowledge * Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) * Applicable pharmaceutical regulations (NOM-059) Education Bachelor’s degree in Pharmacy and Biochemistry or Biochemistry.**Complementary Profile** Equipment and instrument calibration. Descriptive and inferential statistics for data analysis and process performance estimation. At Grupo PiSA, we prohibit violence and discrimination, promoting equal opportunity, inclusion, and diversity. Our selection processes are FREE OF CHARGE; please report any irregularities to lineaeticagrupopisa@letica.email