Contract Quality Validation Engineer - Pharma Cleanrooms

Colgate; Guanajuato; Híbrido; MXN 670.000 - 1.004.000; Jornada completa

Descripción de la vacante

Colgate-Palmolive in Guanajuato, Mexico seeks a Quality Validation Engineer (Temporal) to lead validation activities for critical systems, cleanrooms, and pharmaceutical equipment, ensuring compliance with GMP, FDA, Cofepris, and corporate standards.

The role requires a Bachelor's in Chemical, Industrial, or Mechanical Engineering, 2+ years in pharmaceutical validation, proficiency in validation instrumentation and QA tools, and strong English proficiency.

Formación

• 2+ years of pharmaceutical or high‑compliance manufacturing experience.
• Deep knowledge of Cleaning & Sanitization (C&S) validation.
• Strong understanding of FDA and Cofepris standards.

Responsabilidades

• Lead and execute validation activities for critical systems (HVAC, Water for Injection/Purified Water), cleanroom areas, and specialized pharmaceutical equipment to ensure full compliance.
• Develop and monitor protocols for Cleaning & Sanitization (C&S) validation to eliminate cross-contamination risks.
• Ensure strict adherence to the 26 Corporate Quality Standards and FDA/Cofepris regulations through precise interpretation and implementation of validation requirements.
• Implement procedures and Validation Master Plans (VMPs) defining methodology, activities, and timelines to maintain validated status.
• Manage validation-related change controls and follow up on deviations to ensure accuracy and safety.

Conocimientos

Validation

GMP knowledge

Regulatory compliance

Process Engineering

Quality Management Systems

English proficiency

Educación

Bachelor's degree in Chemical Engineering

Herramientas

Validation instrumentation

Statistical software

Descripción del empleo

Colgate-Palmolive in Guanajuato, Mexico seeks a Quality Validation Engineer (Temporal) to lead validation activities for critical systems, cleanrooms, and pharmaceutical equipment, ensuring compliance with GMP, FDA, Cofepris, and corporate standards.

The role requires a Bachelor's in Chemical, Industrial, or Mechanical Engineering, 2+ years in pharmaceutical validation, proficiency in validation instrumentation and QA tools, and strong English proficiency.