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Ingeniero de Validaciones

Req # JR - 144289 Location Tijuana, Baja California, México Job Category Quality Date posted 08/30/2024
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Overview

This is where you make a difference in our patients’ safety. As a member of the Baxter Quality team, you will play an essential part in our mission of saving and sustaining lives. Quality is important throughout the entire product lifecycle and works collaboratively with all areas of the organization. Because Quality touches everything Baxter does, a role in Quality provides many opportunities for growth, learning and a successful career that has a daily impact on people’s lives.

  • Support for Parents

  • Continuing Education/ Professional Development

  • Employee Heath & Well-Being Benefits

  • Paid Time Off

  • 2 Days a Year to Volunteer

Success Profile

What makes a successful Quality team member at Baxter? Take a look at some of the top traits we’re looking for and see if you’re a fit.

  • Detail Oriented
  • Continuous Learner
  • Courageous
  • Collaborative
  • Critical Thinker
  • Influential

Ingeniero de Validaciones

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Vantive: A New Company Built On Our Legacy

Baxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us.

At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us are driven to help improve patients’ lives worldwide. Join us as we revolutionize kidney care and other vital organ support.

*Completion of the proposed separation of Kidney Care from Baxter into a standalone company (to be named Vantive) remains subject to the satisfaction of customary conditions.

Main Activities and Responsibilities:

  • Monitor compliance with FDA regulatory requirements of countries to which product is exported, international standards (ISO 9001/ISO 13485) and corporate requirements with special attention to 21CFR 820.22, 30, 65, 70, 75, 90, 100, 130, 184, and 198.
  • Statistical analysis of process variation, process/product control, risk analysis of plant product families, implementation of improvement actions resulting from analysis of internal and external product experience data.
  • Ensure compliance with applicable regulations to maintain validation status.
  • Perform qualification and validation process activities.
  • Qualify critical equipment and systems used in manufacturing processes.
  • Comply with the Validation Master Plan in force.
  • Review validation protocols and reports.
  • Collect information attached to validation protocols.
  • Develop and maintain updated procedures applicable to qualification and validation processes according to corporate standards and national and international legislation.
  • Be part of the decision making structure concerning regulatory compliance and quality standards in all the operations described above.
  • Direct support in regulatory inspections.
  • Apply and follow EHS guidelines according to established procedures, standards and official Mexican norms.
  • Supports Quality System compliance by participating in investigations as owner ensuring that activities related to NCR/CAPA follow-up are properly executed, completed and documented.
  • In addition to in case of having participation as a quality approver has the responsibility to ensure that investigations have had adequate cause investigation and that investigation closures or actions have been properly executed, meet system requirements and are properly documented.

Education:

  • Bachelor's degree level in the areas of Industrial Chemist, Chemical Engineer, Industrial Engineer or similar disciplines.

Experience:

  • 2 -3 years of experience in Validations, qualification of manufacturing equipment and critical systems.
  • 2-3 years minimum experience in process validation, analytical methods and computerized systems validation.
  • 2-3 years minimum experience in quality assurance processes, audit execution and manufacturing process implementation.

Knowledge:

  • Advanced English proficiency.
  • Knowledge of computer systems, statistics, equipment qualification.
  • Knowledge in the validation of computerized systems and processes, environmental control and application of local and international regulations applied to document control processes and audits.
  • Knowledge in basic statistics, Six Sigma methodology and risk assessment management.
  • Knowledge of chemical and microbiological laboratory.
  • ERP systems: SAP, TcU, JDEdwards.
  • MDSAP. (Medical Device Single Audit Program) (Desirable).

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

Recruitment Fraud Notice

Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

144289
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Address

Explore this location Blvd. Pacifico #10014 Parque Industrial Pacifico, 2A Seccion
Ecatepec
22643 Tijuana, BCN
Mexico
Explore This Location

Hear from Our Employees

Our company is enriched by a diverse population of individuals in more than 100 countries that work to solve, innovate, manufacture and drive better healthcare options for patients around the world.

Meet Christelle, Senior Quality Manager in Malta

“I was an Engineering Graduate with a Master's in Business Administration, and was more inclined toward working with people than with machines. When I came across an opportunity to work with Baxter as a Quality Engineer, it was the perfect combination: a manufacturing environment and a role that required me to collaborate with multiple teams daily. Baxter's mission of saving and sustaining lives gives me all the purpose and fulfilment I need.”

Meet Lorena, Senior QA Associate in London, UK

“I am registered pharmacist in the UK with experience with drug products and final product release. I am very dedicated to my work and accurate in details to ensure correct assessment is provided to our customers to ensure patients' safety.”

Meet Gary, Quality Research Manager in Singapore

“I have always enjoyed working at Baxter and I find here to be a great place to work! Management truly cares for you, and invests time and resources to support your career goals and aspirations. My current role provides me the opportunity to work with culturally diverse teams, bringing different talents together, learning from one another and working toward a common goal and mission.”

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