VALIDATION ANALYST

Description

Position Summary: Plan and conduct scientific studies for the release and maintenance of validated status for facilities, utilities, equipment, and manufacturing processes. Key Highlights: 1. Plan and execute qualifications and validations 2. Provide technical support for new facility and process projects 3. Work under Good Manufacturing Practices (GMP) **Date:** Apr. 13, 2026 **Address:** 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! **Type of Employee** Confianza**Position Objective** Plan and conduct specific scientific studies for the release of use and maintenance of validated status for facilities, utilities, equipment, computerized systems, spreadsheets, manufacturing, packaging, and cleaning processes, complying with applicable regulatory requirements.**Responsibilities and Activities** * Conduct quality system-related activities under a code of compliance with Good Manufacturing Practices (GMP). * Plan assigned qualifications and validations. * Execute tests defined in the approved qualification/validation protocol, analyze collected data, and generate conclusions regarding equipment/process operation, documenting all information in qualification/validation reports. * Track deviations identified during execution of assigned qualifications or validations. * Provide technical support to Engineering and/or users during new facility, equipment, or process projects. Experience 6 months in: * Validation of processes, areas, utilities, equipment, and systems. * Pharmaceutical, food, cosmetic, or medical device industries. Knowledge * Good Manufacturing Practices (NOM\-059, FDA, Health Canada). * Microsoft Office suite (Word, Excel, PowerPoint). * Descriptive and inferential statistics. * Technical fundamentals of equipment, process, and facility operation and design. Education Bachelor's Degree**Complementary Profile** EXPERIENCE: * Pharmaceutical manufacturing processes. * Design of pharmaceutical facilities. * Physicochemical and microbiological analysis. KNOWLEDGE: * National and international pharmaceutical regulations. * ISO 13485, NOM 241 SSA2, 21 CFR 820\. At Grupo PiSA, we prohibit violence and discrimination, promoting equal opportunity, inclusion, and diversity. Our selection processes are FREE OF CHARGE; report any irregularity to lineaeticagrupopisa@letica.email