VALIDATION ANALYST

Description

Job Summary: Prepare validation documentation reports to ensure compliance and timely identification of the validated status of Grupo PiSA's service companies. Key Highlights: 1. Committed to the health and well-being of millions of people. 2. Be part of a company focused on excellence. 3. An opportunity to transform the future of healthcare. **Date:** Apr 28, 2026 **Address:** ABRAHAM LINCOLN 6235 PASEO DE , NUEVO LEON, 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** Prepare validation documentation reports for equipment, systems, facilities, processes, and facility cleaning to ensure compliance and timely identification of the validated status of Grupo PiSA's service companies. **Responsibilities and Activities** * Plan qualification and validation studies. * Execute qualification and validation tests. 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 operation and design of equipment, processes, and facilities. * NOM (059, 249, 241\), ISO 9001, ISO 13485 * Quality management systems * Metrology Education Bachelor's degree in Chemistry or Chemical-Pharmaceutical Biology **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