Pharma Validation Engineer - Cleanroom & GMP

Colgate-Palmolive; San José Iturbide; Presencial; MXN 420.000 - 660.000; Jornada completa

Descripción de la vacante

Colgate-Palmolive in Guanajuato, Mexico, is seeking a Process and Systems Validation Coordinator to ensure that manufacturing processes, systems, and equipment meet the highest quality and safety standards, especially in cleanroom and pharmaceutical environments.

You will lead Validation Master Plans and align plant operations with FDA and Cofepris standards, guiding validation projects from planning to execution, including change control and audits.

Formación

• 2+ years of pharmaceutical or high-compliance manufacturing experience.
• Experience validating cleanrooms, critical systems and equipment.
• Knowledge of FDA and Cofepris standards for Pharma/API environments.

Responsabilidades

• Lead validation activities for HVAC, WFI/Purified Water, cleanrooms and equipment to ensure compliance.
• Develop and monitor protocols for Cleaning & Sanitization validation to prevent cross-contamination.
• Ensure adherence to 26 Corporate Quality Standards and regulatory requirements.
• Act as SME during internal and external audits, providing technical evidence for validation strategies.

Conocimientos

English proficiency

Validation instrumentation

Statistical software

Educación

Bachelor's degree in Chemical Engineering (preferred)

Industrial or Mechanical Engineering

Herramientas

Validation instrumentation

Specialized validation software

Descripción del empleo

Colgate-Palmolive in Guanajuato, Mexico, is seeking a Process and Systems Validation Coordinator to ensure that manufacturing processes, systems, and equipment meet the highest quality and safety standards, especially in cleanroom and pharmaceutical environments.

You will lead Validation Master Plans and align plant operations with FDA and Cofepris standards, guiding validation projects from planning to execution, including change control and audits.