
Expert, Validation analytique QC Lab - CDD 6 mois
Descrição geral
Ser um engenheiro na Baxter significa que você desempenha um papel fundamental para nos ajudar a cumprir nossa missão de salvar e prolongar vidas. Desde o projeto de produtos inovadores até a produção e a entrega ao paciente, nossos engenheiros são cruciais para entregar resultados para nossos clientes e pacientes em todo o mundo.
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Apoio aos pais
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Educação continuada / Desenvolvimento profissional
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Benefícios de saúde e bem-estar para funcionários
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Férias remuneradas
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2 dias por ano para trabalho voluntário
Perfil de sucesso
O que torna um engenheiro bem-sucedido na Baxter? Confira algumas das principais características que procuramos e veja se o seu perfil se encaixa.
- Solucionador de problemas
- Pensador analítico
- Orientado por dados
- Focado em soluções e orientado a resultados
- Colaborativo
- Inovador
Expert, Validation analytique QC Lab - CDD 6 mois
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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Junte-se à nossa comunidade de talentos
Agradecemos seu interesse em uma carreira na Baxter e gostaríamos de conhecê-lo. Participar da nossa comunidade de talentos é uma ótima maneira de estar conectado, aprender mais sobre a Baxter e ajudar nossos recrutadores a te encontrar caso houver uma oportunidade que se alinhe com sua experiência, habilidades e interesses.