VALIDATION ANALYST

Description

Job Summary: Plan and conduct scientific studies for the release and maintenance of validated facilities, equipment, and processes, in compliance with regulations. Key Highlights: 1. Part of a Mexican company committed to health. 2. An opportunity to live "A Life in Service of Life". 3. Work within a team focused on excellence and growth. **Date:** May 15, 2026 **Address:** Rivera de Champayan 109\-A\-INT , TAMAULIPAS, 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 health and leave a positive mark on the world! **Employment Type** Confidential **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, 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 authorized protocols and analyze results. * Track identified deviations. * Provide technical support to Engineering and users for new facility, equipment, or process projects. * Perform 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 operation and design of equipment, processes, and facilities. 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, and 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 OF CHARGE; report any irregularity to lineaeticagrupopisa@letica.email