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QA Releaser Compounding

Req # JR - 180116 Location Thetford, England, United Kingdom Job Category Quality Date posted 07/18/2025
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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

Expert, Validation analytique QC Lab - CDD 6 mois

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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.

VOTRE MISSION

L’expert, Validation QC Lab assure la gestion des validations, vérifications, transferts de méthodes analytiques au laboratoire QC, à travers des projets de remédiation/amélioration. Il/elle participe à la mise en conformité par rapport aux pharmacopées. Il/elle assure également l’évaluation de la revue périodique des fichiers Excel utilisés au laboratoire QC par l’équipe en charge du release. Il/elle documente son travail dans les systèmes qualités adéquats.  

VOS RESPONSABILITES

  • Participer à la mise en place de nouveaux projets (de remédiation ou d’amélioration) : Effectuer les tests préliminaires / Rédiger les protocoles et rapports afin de valider/vérifier ou transférer des méthodes analytiques, en accord avec les guidances en vigueur / Effectuer les tests requis et/ou effectuer les révisions qui s’imposent lors de validation/transfert/vérification de méthodes analytiques. : Documenter ces nouveaux projets dans les systèmes qualités adéquats.

  • Assurer la validation et l’évaluation de la revue périodique des feuilles excel utilisées pour le release.

  • Participer à la mise en place des changements de pharmacopées ou de nouvelles méthodes (deuxième série et révision de la documentation).

  • Former les analystes sur les méthodes dans le cadre d’une validation/vérification ou transfert.

  • Se positionner comme une personne de référence pour ses activités.

  • Prendre les tâches de back up selon les besoins de l’équipe

  • Assurer la mise en conformité des procédures et processus avec les requis légaux (EP, USP, dossier d’enregistrement,) et avec les documents corporate.

  • Apporter son support à l’équipe release en cas de besoin et suivant ses compétences.

  • Gère ses projets en autonomie

  • 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.

VOTRE PROFIL

  • Vous êtes issu d’une formation scientifique, Bachelier ou Master en chimie ou en Biotechnologie

  • Vous avez une première expérience dans une fonction similaire en validation de méthodes analytiques

  • 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.

  • Vous êtes Respectueux des règles et des procédures

  • Rigoureux, capacité d’organisation et de planification

  • Bon communicateur

  • Esprit de synthèse

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 Baxter Healthcare Ltd
Pharmacy Services, Caxton Way
Thetford
Norfolk
IP24 3SE
United Kingdom
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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