
Quality Compliance Manager
Descrição geral
É aqui que você faz a diferença na segurança de nossos pacientes. Como membro da equipe de Qualidade da Baxter, você desempenhará uma função essencial em nossa missão de salvar e prolongar vidas. A qualidade é importante em todo o ciclo de vida do produto e trabalha de forma colaborativa com todas as áreas da organização. Como a Qualidade afeta tudo o que a Baxter faz, uma função na Qualidade oferece muitas oportunidades de crescimento, aprendizado e uma carreira de sucesso que afeta a vida das pessoas todos os dias.
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Suporte aos pais
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Educação continuada/ Desenvolvimento profissional
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Benefícios de saúde e bem-estar dos 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 membro da equipe de qualidade da Baxter bem-sucedido? Confira algumas das principais características que estamos procurando e veja se o seu perfil se encaixa.
- Orientado para os detalhes
- Aprendiz contínuo
- Corajoso
- Colaborativo
- Pensador crítico
- Influente
Quality Compliance Manager
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.
Chez Baxter Healthcare Corporation, nous sommes engagés à sauver et préserver des vies grâce à des produits et services médicaux innovants. Notre équipe est passionnée de faire la différence et nous avons été reconnus comme un "Great Place to Work" pour la 7ème année consécutive. Rejoignez-nous dans notre mission et devenez partie prenante d'une industrie dynamique et en évolution.
Ce que vous ferez :
Gestion des audits
Participer aux audits externes : être référent pour les organismes de certification
Piloter les audits internes : organiser ces audits et coordonner les auditeurs
Suite aux audits, proposer les plans d’actions, contrôler leur réalisation et vérifier leur efficacité
Garantir la communication liée aux audits (préparation, résultats, …)
Pertinence, adéquation, efficacité et efficience du Système Qualité
Vérifier l’adéquation du SMQ avec l’évolution des exigences externes et internes, et avec les processus
Aider à la préparation des revues de direction et comités de pilotage
Participer à l’amélioration continue du SMQ
Gestion documentaire
Conseiller les services dans la mise en œuvre de leur organisation Qualité
Former les utilisateurs à l’outil de gestion du système documentaire
Assurer la vérification et l'approbation des documents et leur cohérence avec le Système Qualité
Participer à la traduction des documents applicables au site
Gestion des Actions Correctives & Préventives
Participer à la détection des écarts au SMQ
Former et conseiller les services dans l’application du processus CAPA
Gérer les indicateurs de gestion des CAPA
Être le référent du site pour les CAPA
Management du Service
Manager les ingénieurs et techniciens du service
Mener les entretiens de performance des subordonnés
Gérer le personnel et la permanence des missions du service (congés, remplacement)
Superviser les activités qualité de Master Validation Plan, IQ, OQ, and PQ des équipements et process.
Promotion – Formation
Promouvoir le SMQ
Former et conseiller les services dans l’application des nouvelles exigences
Développer & proposer les formations adéquates, afin d’accroître la compréhension et l’adhésion au SMQ
Suivi des indicateurs de formation du site.
Ce que vous apporterez :
Formation niveau Bac+5 en ingénierie, qualité ou équivalent.
Expérience professionnelle (l’un ou l’autre) :
5 ans dans un milieu industriel rattaché aux plus grands référentiels qualité (Pharmaceutique, aéronautique, FDA, ISO 13485, …)
2 ans dans un service qualité, intégré à une entreprise du milieu industriel des dispositifs médicaux
Management d’équipe
Maîtrise de l’anglais
Maîtrise des outils bureautiques, de gestion documentaire, analyse de données et tendances.
Esprit de synthèse
Maîtrise des référentiels Qualité applicables, ISO 13485, ISO 9001, FDA 21 CFR Part 820
Expérience dans la réglementation et Inspection FDA
Connaissance des principes de l’amélioration continue
Force de proposition
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.
Endereço

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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.