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Validation Engineer - 6 months temporary role

Req # JR - 186139 Location San Vittore, Grisons, Switzerland Job Category Quality Date posted 09/12/2025
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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

Validation Engineer - 6 months temporary role

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This is where your work makes a difference.

At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job—you will find purpose and pride. 

The validation engineer is critical in ensuring that all validation activities are executed in compliance with regulatory

standards and Baxter's internal quality requirements. The validation engineer will work closely with cross-functional

teams to develop, implement, and maintain validation protocols and documentation.

WHAT YOU'LL BE DOING:

Validation Planning: Develop and execute validation plans for the Line 2 downstream upgrade project,

ensuring alignment with project timelines and regulatory requirements.

· Protocol Development: Create, review, and approve validation protocols, including Installation Qualification

(IQ), Operational Qualification (OQ), and Performance Qualification (PQ) documents.

· Execution of Validation Activities: Conduct validation activities, including testing and data analysis, to

ensure that all systems and processes meet defined specifications and performance criteria.

· Collaboration: Work closely with engineering, manufacturing and quality teams to ensure seamless

integration of validation activities into the project lifecycle.

· Documentation: Maintain accurate and comprehensive validation documentation, including reports,

deviations, and change controls, in accordance with Good Manufacturing Practices (GMP) and Baxter's

quality standards.

· Risk Assessment: Perform risk assessments related to validation activities and implement appropriate

mitigation strategies.

· Training and Support: Provide training and support team members on validation processes and best

practices.

· Continuous Improvement: Identify opportunities for process improvements and contribute to the

development of validation strategies that enhance efficiency and compliance.

WHAT YOU'LL BRING:

Bachelor’s degree in engineering, Life Sciences, or a related field good knowledge of English language

Minimum of 3 years of experience in validation engineering within the pharmaceutical, biotechnology, or medical

device industries, with a focus on downstream processing

Strong understanding of validation principles and quality systems (ISO, cGMP).

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

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.

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Address

Explore this location Sapa Prodotti Plastici S.A. Zona Niscio
6534 6534 S. Vittore GR
Switzerland 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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