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Expert Qualification et Validation aux laboratoires QC

Req # JR - 144320 Location Lessines, Wallonia, Belgium Job Category Quality Date posted 10/15/2024
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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

Expert Qualification et Validation aux laboratoires QC

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This is where you save and sustain lives

At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.

RESUME DE LA FONCTION

L’ expert qualification et validation aux laboratoires QC assure la gestion, la maintenance et la qualification des instruments de laboratoire et systèmes informatisés liés.  Il/elle se positionne comme personne de référence pour les équipements de laboratoire et initie ou participe aux projets d’amélioration (digitalisation entre autres).

TACHES GENERALES

  • Participer à la validation de nouveaux équipements : rédiger les documents de qualification des instruments/software ainsi que les procédures liées, en accord avec les bonnes pratiques de laboratoire et autres standards.
  • Participer à la réalisation des qualifications (tests sur les équipements/softwares)
  • Être le point de contact des fournisseurs (achat de nouveaux équipements, back up pour la planification et suivi des maintenances, réparations).
  • Participer à la gestion du cycle de vie des instruments (enlèvement, déplacement, maintenance).
  • Assurer la formation du personnel aux nouvelles procédures et à l’utilisation des nouveaux équipements.
  • Assurer la documentation des évènements de calibration des hors-limites et des interventions sur les équipements selon les procédures en vigueur et en utilisant les outils adaptés (en tant que back up pour la rédaction ou en tant que reviewer).
  • Gérer les accès sur les instruments
  • Participer à l’élaboration des commandes/contrats liés aux instruments. (être le point de contact des fournisseurs)
  • Gérer les demandes de tests et documentations associées aux requis des tests « elemental impurities »
  • Apporte son support à l’équipe release en cas de besoin et suivant ses compétences.
  • Participer activement aux initiatives d’amélioration des processus liés aux activités du laboratoire.
  • Assurer le suivi de son plan de formation dans les délais impartis et vérifier que celui-ci est complet.
  • Remonter à son superviseur tout incident/retard pouvant affecter la tenue des targets définis pour les projets et autres activités.
  • Être le relais du superviseur dans le cadre des activités de routine (ex : planification des activités)

PROFIL RECHERCHE

  • Vous êtes issu d’une formation scientifique, et/ ou avez une expérience dans une fonction similaire en validation d’équipement
  • Vous disposez de bonnes connaissances d’anglais
  • Vous êtes à l’aise avec les logiciels IT, notamment la suite Office
  • Vous faites preuve de prise d’initiatives et êtes autonome dans la résolution de problèmes techniques

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.

144320
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Address

Explore this location Rue Rene Branquart, 80
7860 Lessines
Belgium
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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