
Expert, Validation analytique QC Lab
Overview
Being an Engineer at Baxter means you play a critical role in helping us achieve our mission to save and sustain lives. From innovative product design through to production and patient delivery, our Engineers are key to delivering results for our customers and patients worldwide.
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Support for Parents
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Continuing Education/ Professional Development
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Employee Heath & Well-Being Benefits
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Paid Time Off
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2 Days a Year to Volunteer
Success Profile
What makes a successful Engineer at Baxter? Take a look at some of the top traits we’re looking for and see if you’re a fit.
- Problem Solver
- Analytical Thinker
- Data Driven
- Solution Focused & Results Oriented
- Collaborative
- Innovative
Expert, Validation analytique QC Lab
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
#LI-BAXGEN
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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