VALIDATION ANALYST

Description

Job Summary: Plan and conduct scientific studies for the release of use and maintenance of validated status for facilities and processes, complying with regulatory requirements. Key Highlights: 1. Committed to the health and well-being of millions of people. 2. Be part of a company where every day is an opportunity. 3. Contribute to transforming the future of healthcare. **Date:** Apr 13, 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! **Employee Type** Confidence **Job Objective** Plan and conduct specific scientific studies for the release of use and maintenance of validated status for facilities, services, equipment, computerized systems, spreadsheets, manufacturing, packaging, and cleaning processes, complying with applicable regulatory requirements. **Responsibilities and Activities** * Conduct quality system activities under a code of compliance with Good Manufacturing Practices (GMP). * Plan assigned qualifications and validations. * Execute tests defined in approved protocols and analyze results. * Track identified deviations. * Provide technical support to Engineering and end users for new facility, equipment, or process projects. * Execute validation of computerized systems and spreadsheets. Experience 6 months in: * Validation of processes, areas, services, 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 **Additional 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. Experience Certifications Language At Grupo PiSA, we prohibit violence and discrimination, promoting equal opportunities, inclusion, and diversity. Our selection processes are FREE; report any irregularity to lineaeticagrupopisa@letica.email