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Profesional de Validaciones (Temporal)

AstraZeneca

Mexico - Lomas Verdes part_time

Posted: March 11, 2026

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Quick Summary

We are seeking a profesional de Validaciones (Temporal) to develop and implement projects to ensure compliance with local and corporate norms, verifying the robustness, reliability, and reproducibility of processes and equipment in the LV plant.

Job Description

Profesional de Validaciones (Temporal) - AstraZeneca Lomas Verdes

Proveer servicios de tecnología e ingeniería de proyectos para apoyar las operaciones de negocios en la planta de LV. Verifica el cumplimiento de la normatividad local y corporativa, asegurando la robustez, confiabilidad y reproducibilidad de los procesos del sitio. Ejecuta las actividades derivadas del Plan maestro de Validación, así como las verificaciones para garantizar el mantenimiento al estado validado de procesos y calificado de equipos, sistemas críticos e instalaciones.

Responsabilidades:

• Desarrollar e implementar el Plan Maestro de Calificación/Validacion de los proyectos asignados a través del portafolio de proyectos y/o el programa del Plan Maestro de Validación del sitio.
• Elaborar y/ revisar documentación técnica y regulatoria incluida pero no limitada a controles de cambios, procedimientos, planes maestros de calificación/validación, protocolos de calificación / validación, protocolos de transferencia de tecnología, teportes técnicos
• Elaborar, ejecutar y/o revisar la calificación de equipos, validación de procesos, validaciones de limpieza y “start-up” de procesos, equipos, sistemas y transferencias de tecnología de procesos existentes.
• Cubrir proyectos del sitio de AstraZeneca Lomas Verdes en validación de limpieza y calificación de sistemas críticos (HVAC, aire comprimido y agua potable)
• Desarrollar y mantener sistemas para establecer estándares (prácticas) relativos a sistemas críticos.
• Proveer experiencia técnica, capacitación y entrenamiento (cuando aplique) y solución de problemas. Estar actualizado con respecto a la especialización o práctica.

Requerimientos

• Licenciatura en QFB, QFI o afín
• Experiencia en Buenas Prácticas de Fabricación y Documentación
• Conocimiento en sistemas documentales electrónico
• Conocimiento en revisiones periódicas 
• Calificación de sistemas críticos
• Validación de limpieza 
• Inglés intermedio

Deseable

• Manejo de sistemas SAP & VEEVA
• Inglés avanzando
• Proactividad a proyectos de mejora

AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

Date Posted

10-mar-2026

Closing Date

28-mar-2026

AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

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