20 publicaciones de empleo destacadas de projects quality en parque industrial querétaro, que (¡Están contratando!)

Quality Validation Engineer (Temporal)
Colgate-Palmolive —San José Iturbide, Gto.
- Por temporada
- Administración de personal
- Inglés
- Licenciatura
8d
SDE
IMI Plc - Legacy Precision —Parque Industrial Querétaro, Qro.
- Tiempo completo
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Purchasing Manager
IMI Plc - Legacy Precision —Parque Industrial Querétaro, Qro.
- Tiempo completo
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Master Planner
Colgate-Palmolive —San José Iturbide, Gto.
- Administración de personal
- Inglés
- Maestría
8d
Quality Trainee
IMI Plc - Legacy Precision —Parque Industrial Querétaro, Qro.
- Inglés
Postulación rápida
Packaging Engineer
Colgate-Palmolive —San José Iturbide, Gto.
- Administración de personal
- ERP systems
- Inglés
2d
Continuous Improvement Engineer
IMI Plc - Legacy Precision —Parque Industrial Querétaro, Qro.
- Tiempo completo
- Inglés
- Licenciatura
- Mejora continua
Quality engineer
ZF —Santa Rosa de Jáuregui, Qro.
- Inglés
Accountant IV, Accounting
Gates Corporation —San José Iturbide, Gto.
- Microsoft Excel
- Administración de personal
- ERP systems
9d
Manufacturing Systems Specialist
Colgate-Palmolive —San José Iturbide, Gto.
- Administración de personal
- Inglés
- Licenciatura
13d
Quality Trainee
IMI plc —Parque Industrial Querétaro, Qro.
- Inglés
Senior Product Engineer
IMI plc —Parque Industrial Querétaro, Qro.
- Tiempo completo
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
6d
Senior Product Engineer
IMI Plc - Legacy Precision —Parque Industrial Querétaro, Qro.
- Tiempo completo
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Electromechanical Technician
IMI Plc - Legacy Precision —Parque Industrial Querétaro, Qro.
- Tiempo completo
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Engineering Manager
Eaton —Santa Rosa de Jáuregui, Qro.
- Bilingüe
- Administración de personal
- Maestría
Controls Engineer
The Timken Company —San José Iturbide, Gto.
- Inglés
- Controlador Lógico Programable
- Licenciatura
Master Data Administrator
Flowserve —Querétaro, Qro.
- Microsoft Excel
- Oracle
- ERP systems
Postulación rápida
SR MANUFACTURING ENGINEER
AIRBUS HELICOPTERS MEXICO QUERETARO, S.A. DE C.V. —Santiago, Qro.
- Tiempo completo
- Inglés
- Ensamblaje
- Mejora continua
2d
Senior Cost Accountant
Flowserve, S. de R.L. de C.V. (Mexico) —Querétaro, Qro.
- Microsoft Excel
- Oracle
- Licenciatura
Postulación rápida
14d
Maintenance Supervisor
Eaton —Santa Rosa de Jáuregui, Qro.
- Mantenimiento
- Ensamblaje
- Licenciatura
9d

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Quality Validation Engineer (Temporal)

Colgate-Palmolive -
San José Iturbide, Gto.

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Información del empleo

Por temporada
Hace 8 días

Cualificaciones

Software estadístico
Ingeniería mecánica
Administración de personal
Inglés
Licenciatura
HVAC
Limpieza
Experiencia en manufactura
Liderazgo

Descripción completa del empleo

No Relocation Assistance Offered
Job Number #175076 - San Jose Iturbide, Guanajuato, Mexico

Who We Are

Colgate-Palmolive Company is a global consumer products company operating in over 200 countries specialising 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.

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 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 people—developing 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, colour, 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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projects quality empleos en parque industrial querétaro, que

Quality Validation Engineer (Temporal)

SDE

Purchasing Manager

Master Planner

Quality Trainee

Packaging Engineer

Continuous Improvement Engineer

Quality engineer

Accountant IV, Accounting

Manufacturing Systems Specialist

Quality Trainee

Senior Product Engineer

Senior Product Engineer

Electromechanical Technician

Engineering Manager

Controls Engineer

Master Data Administrator

SR MANUFACTURING ENGINEER

Senior Cost Accountant

Maintenance Supervisor

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