Quality Validation Engineer (Temporal)

Colgate

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profile Job Location:

Ocosingo - Mexico

profile Monthly Salary: Not Disclosed
Posted on: Yesterday
Vacancies: 1 Vacancy

Job Summary

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 valuesCaring Inclusive and Courageouswe foster a culture that inspires our people to achieve common goals. Together lets 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 equipmentparticularly withincleanroom and pharmaceutical environmentscomply 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 the26 Corporate Quality StandardsFDA andCofeprisregulations 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:Bachelors 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 pharmaceutical clean areas.

  • Regulatory Expertise:Deep knowledge of FDA and Cofepris standards (specifically for Pharma/API environments).

  • Technical Mastery:Solid understanding of Process Engineering Good Manufacturing Practices (GMP) and Quality Management Systems.

  • Languages:Intermediate-Advanced English proficiency.


Desired Qualifications

  • Instrumentation & Software:Hands-on experience with validation instrumentation and specialized validation/statistical software.

  • Project Management: Ability to coordinate multiple complex validation projects and manage contractor personnel simultaneously with high attention to detail.


Our Commitment to Inclusion
Our journey begins with our peopledeveloping strong talent with diverse backgrounds and perspectives to best serve our consumers around the world and fostering an inclusive environment where everyone feels a true sense of belonging. We are dedicated to ensuring that each individual can be their authentic self is treated with respect and is empowered by leadership to contribute meaningfully to our business.

Equal Opportunity Employer
Colgate is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race color religion gender gender identity sexual orientation national origin ethnicity age disability marital status veteran status (United States positions) or any other characteristic protected by law.

Reasonable accommodation during the application process is available for persons with disabilities. Please complete this request form should you require accommodation.

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Required Experience:

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No Relocation Assistance OfferedJob Number#173414 - San Jose Iturbide Guanajuato MexicoWho We AreColgate-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 ...
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Descubra el Centro de información de cuidado bucal y dental de Colgate. El Centro de información de cuidado bucal y dental suministra información sobre salud dental, productos de salud bucal y mucho más. Enjuague bucal, crema dental, cepillo dental, cepillo de dientes eléctrico.

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