Validation Engineer, QA
Descripción general
Aquí es donde usted marca la diferencia en la seguridad de nuestros pacientes. Como miembro del equipo de Calidad de Baxter, desempeñará un papel esencial en nuestra misión de salvar y sostener vidas. La calidad es importante durante todo el ciclo de vida del producto y trabaja en colaboración con todas las áreas de la organización. Debido a que Calidad afecta todo lo que hace Baxter, un rol en Calidad brinda muchas oportunidades de crecimiento, aprendizaje y una carrera exitosa que tiene un impacto diario en la vida de las personas.
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Apoyo a las padres
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Educación continua/ Desarrollo profesional
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Salud de los empleados y Beneficios de bienestar
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Tiempo libre pagado
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2 días al año para ser voluntario
Perfil de éxito
¿Qué hace que un miembro del equipo de calidad de Baxter sea exitoso? Revise algunos de los rasgos principales que estamos buscando y vea si su perfil se ajusta.
- Orientado al detalle
- Aprendiz continuo
- Valiente
- Colaborativo
- Pensador crítico
- Influyente
Validation Engineer, QA
This is where your work makes a difference.
At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.
Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.
Here, you will find more than just a job—you will find purpose and pride.
LE JOB
Assurer les activités de validation de routine et associés aux projets pour les équipements et procédés du département Sterile Drugs et Plastics en compliance avec les standards GMP et les requis internes de validation.
TACHES GENERALES
Maintient le statut validé des équipements et des procédés en réalisant les évaluations périodiques selon les plannings en vigueur
Fournit une expertise validation et qualité pour le développement des projets.
Implication directe dans la définition des spécifications et analyse de risque des process/systèmes.
Revoit et approuve les URS/FS/DS sur les requis validation et qualité.
Définit les stratégies de validation.
Rédige la documentation validation en compliance avec les requis Baxter et cGMP et s’assure de l’application de ces requis (protocoles et rapports).
Organise et coordonne les activités de validation avec les différents départements impliqués en respectant les planning définis. Réalise les trainings associés aux tests.
Analyse, interprète, documente et approuve en tant que QA les résultats de test.
Gère les non-conformités de validation.
Maintient le statut validé des équipements/procédés suite aux modifications documentées dans le process de change control : assessment des changements, approbation des tests, clôture des tâches.
Met à jour les procédures et annexes du département validation selon les réglementations.
Distribue les documents de validation selon procédures en vigueur.
Approuve QA les documents de validation du labo QC.
Fournit les données validation selon les demandes Regulatory, R&D, etc…
Propose des suggestions pour l'amélioration des process et benchmark les bonnes pratiques de validation (interne et externe).
Réalise les audits internes du site selon le planning défini.
Participe aux audits externes et clôture les observations d’audits internes et externes.
Collecte et analyse les données validation pour les APQR et MMR.
S’assure que le planning release des produits est respecté.
PROFIL RECHERCHE
Bachelier ou Ingénieur en Sciences
Avoir 3 années d’expérience minimum dans une fonction équivalente en validation
Avoir une parfaite maitrise du français et très bonne connaissance de l’anglais
Etre orienté solutions avec un bon esprit critique
Team-player et orienté travail en équipe
Bonne connaissance des GMPs
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.
Dirección
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