VALIDATION ANALYST

Description

**Date:** Oct. 22, 2025 **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 mark on the world! **Employee Type** Confidential **Complementary Profile** **1\.** **Key Responsibilities:** 1\.1 Conduct quality system-related activities in compliance with Good Manufacturing Practices (GMP). 1\.2 Plan assigned equipment and instrument qualification and validation activities to ensure they are scheduled and executed properly. 1\.3 Execute tests defined in the approved qualification/validation protocol, analyze collected data, draw conclusions regarding equipment/process operation, and document all information in qualification/validation reports. 1\.4 Track deviations identified during the execution of assigned qualifications or validations. 1\.5 Provide technical support to Engineering and/or end users during new facility, equipment, or process projects. **2**. **Education Level:** 2\.1 Chemical Engineering, Pharmaceutical Biologist, or related degree. Degree certificate and/or letter of completion. 3\. Experience: 3\.1 In qualification/validation of areas, systems, equipment, and processes. At Grupo PiSA, we prohibit violence and discrimination, promoting equal opportunity, inclusion, and diversity. Our selection processes are FREE OF CHARGE; please report any irregularity to lineaeticagrupopisa@letica.email