Quality Validation Engineer (Temporal)

No Relocation Assistance Offered Job Number #173414 - San Jose Iturbide, Guanajuato, Mexico Who We Are Colgate-Palmolive Company is a global consumer products company operating in over 200 countries specializing in Oral Care, Personal Care, Home Care, Skin Care, and Pet Nutrition. Our products are trusted in more households than any other brand in the world, making us a household name! Join Colgate-Palmolive, a caring, innovative growth company reimagining a healthier future for people, their pets, and our planet. Guided by our core values—Caring, Inclusive, and Courageous—we foster a culture that inspires our people to achieve common goals. Together, let's build a brighter, healthier future for all.   Role Summary The Process and Systems Validation Coordinator is a high-level technical role responsible for ensuring that all manufacturing processes, systems, and equipment—particularly within  cleanroom and pharmaceutical environments —comply with the highest quality and safety standards. This role leads the implementation of Validation Master Plans (VMP) to guarantee system consistency and accuracy. By aligning plant operations with the  26 Corporate Quality Standards ,  FDA , and  Cofepris  regulations, this position is critical in maintaining product purity and ensuring full regulatory readiness. Key Responsibilities Critical Systems Validation:  Lead and execute validation activities for critical systems (HVAC, Water for Injection/Purified Water), cleanroom areas, and specialized pharmaceutical equipment to ensure full compliance. Specialized Protocols:  Develop and monitor specific protocols for Cleaning & Sanitization (C&S) validation, ensuring that all procedures effectively eliminate cross-contamination risks. Regulatory & Corporate Compliance:  Ensure strict adherence to the 26 Corporate Quality Standards and NOM/FDA/Cofepris regulations through the precise interpretation and implementation of validation requirements. Validation Master Planning:  Implement procedures and VMPs that define the methodology, activities, and timelines required to maintain the validated status of the entire plant. Change Control & Deviation Management:  Manage validation-related change controls and provide rigorous follow-up on deviations, ensuring all technical functions remain accurate and safe for the intended use. Audit Leadership:  Act as a subject matter expert (SME) during internal and external corporate audits, providing technical evidence and defending validation strategies to regulatory bodies. Required Qualifications Education:  Bachelor’s degree in Chemical Engineering (preferred), Industrial, or Mechanical Engineering. Experience:  2+ years of experience in pharmaceutical or high-compliance manufacturing operations, with a proven track record in validating cleanrooms, critical systems and equipment. Specialized Knowledge:  Deep understanding of Cleaning & Sanitization (C&S) validation and the management of…