VALIDATION ANALYST

Description

Job Summary: Prepare validation documentation reports to ensure compliance and timely identification of the validated status of Grupo PiSA companies. Key Highlights: 1. Committed to the health and well-being of millions of people 2. An opportunity to live "A Life in Service of Life" 3. Part of a Mexican company with over 80 years of history **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** Trust-based **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 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 Pharmacy 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 recruitment processes are FREE OF CHARGE; please report any irregularities to lineaeticagrupopisa@letica.email