VALIDATION ANALYST

Description

Job Summary: Conduct and document validation and qualification studies for manufacturing processes, critical systems, equipment, and facilities to ensure regulatory and quality compliance. Key Highlights: 1. Commitment to health and well-being 2. Opportunity to transform the future of healthcare 3. Being part of a company dedicated to excellence **Date:** Mar 10, 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! **Employment Type** Confidential **Job Objective** Conduct and document applicable validation and qualification studies for manufacturing processes, critical systems, equipment, areas, and facilities, ensuring compliance with established regulatory requirements and quality standards. **Responsibilities and Activities** 1. Execute equipment, system, and process validation studies according to technical specifications and current regulations. 2. Ensure equipment is in proper working condition, meeting operational and maintenance specifications. 3. Ensure all documentation complies with applicable regulatory and statutory requirements, and maintain its validity through detailed validation activity reports. 4. Identify protocol acceptance criteria failures and/or deviations from the processes under evaluation, and address them to closure. 5. Ensure validation is performed in accordance with established procedures to meet industry pharmaceutical quality standards and regulations. Experience - Qualification and validation processes for areas, utilities, equipment, and processes. - 1 Year - Pharmaceutical or food industry - 1 Year Knowledge - Proficiency in Microsoft Office Suite - Intermediate * National Good Manufacturing Practices (NOM-059), U.S. FDA, and Health Canada regulations Education Bachelor's degree in Pharmacy and Biochemistry or Biochemistry **Complementary Profile** Equipment and instrument calibration Descriptive and inferential statistics for data analysis and process performance estimation. Experience Certifications Language At Grupo PiSA, we prohibit violence and discrimination, promoting equal opportunity, inclusion, and diversity. Our selection processes are FREE OF CHARGE; report any irregularities to lineaeticagrupopisa@letica.email