VALIDATION ANALYST

Description

Job Summary: Plan and execute scientific studies for the validation and maintenance of facilities, services, equipment, and processes, ensuring regulatory compliance. Key Highlights: 1. Commitment to health and wellness with over 80 years of history 2. Working in a team focused on excellence and continuous growth 3. Opportunity to transform the future of healthcare **Date:** Apr 22, 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 wellness 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! **Employment Type** Trust-based **Job Objective** Plan and conduct specific scientific studies for the release of use and maintenance of the validated status of facilities, services, equipment, computerized systems, spreadsheets, manufacturing processes, conditioning, and cleaning, 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 authorized protocols and analyze results. * Follow up on identified deviations. * Provide technical support to Engineering and users for new facility, equipment, or process projects. * Execute computerized system and spreadsheet validations. 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 in Chemical-Pharmaceutical or Chemical-Biological fields. **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, and 21 CFR 820 standards. At Grupo PiSA, we prohibit violence and discrimination, promoting equal opportunities, inclusion, and diversity. Our selection processes are FREE OF CHARGE; report any irregularity to lineaeticagrupopisa@letica.email