Microbiologist (Evergreen)
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.
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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 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
Microbiologist (Evergreen)
Vantive: A New Company Built on Our Legacy
Since last year, Baxter has been on a journey to separate our Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us.
At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us are driven to help improve patients’ lives worldwide. Join us as we revolutionize kidney care and other vital organ support.
*Completion of the proposed sale of Vantive to funds managed by the Carlyle Group is subject to receipt of customary regulatory approvals and satisfaction of other closing conditions.
Objetivo principal del puesto:
Persona responsable de las labores asignadas a su cargo desde el punto de vista operativo en el Laboratorio de Calidad tanto en el área de Química como en el área de Microbiología. Coordinador del área en cumplimiento con las regulaciones aplicables al área. Dar soporte en la gestión, planeación, evaluación, ejecución y control de los procesos que afectan las condiciones ambientales de cuartos limpios y producto, optimizando la utilización de los recursos disponibles y previniendo problemas de contaminaciones biológicas o físico-químicas minimizando su impacto.
Principales Actividades y Responsabilidades:
1. Responsable del cumplimiento de los controles establecidos en los procedimientos para análisis
microbiológicos relacionados con el control ambiental de la planta y de los sistemas críticos:
microorganismos en aire, microorganismos en superficies, microorganismos en aire comprimido,
microorganismos en agua de planta y monitoreo de partículas no viables.
2. Otorgar soporte en la realización de los análisis microbiológicos de producto terminado, materia prima y
material de empaque de productos estériles y no estériles.
3. Realizar los siguientes Monitoreos:
a. Monitoreo de cloro en el agua de extrusoras.
b. Monitoreo de cloro del sistema de agua.
c. Monitoreo de presiones diferenciales.
d. Monitoreo microbiológico del agua de la extrusoras.
e. Monitoreo de partículas, microbiológico e hidrocarburos del sistema de aire comprimido.
f. Monitoreo de las condiciones ambientales del equipo y área de laboratorio.
g. Monitoreo microbiológico de personal.
h. Monitoreos ambientales extraordinarios por cambios programados o no conformidades.
i. Monitoreo de partículas viables.
j. Monitoreo de partículas no viables.
4. Responsable del control de análisis relacionados con producto final: bioburden, pirógenos y pruebas de
release.
5. Controlar y liberar producto final estéril fabricado en la planta para estar en cumplimiento con los
requerimientos del Sistema de Calidad, en caso de ser requerido por el Ingeniero de Esterilización.
6. Gestionar investigaciones ambientales en caso de exceder los límites de alerta y acción, emitiendo opinión
técnica de la causa de la falla, así como el de dar seguimiento con los responsables del área a las
acciones correctivas y preventivas correspondientes, y su despliegue de acuerdo a procedimientos.
7. Coordinar la elaboración y envió de muestras necesarias para el programa verificación de carga biológica
en coordinación con producción, y control de calidad proceso, en caso de ser requerido por el Ingeniero de
Esterilización.
8. Mantener el control de los archivos, registros y expedientes del programa de verificación de carga biológica. 9. Brindar atención a las siguientes actividades: a. Calculo de límites, revisión periódica y análisis de tendencias de parámetros y controles ambientales. b. Recibe, verifica y determina la condición adecuada de materiales y equipos. c. Coordina el almacenamiento o entrega de materiales y equipos para su disposición, ajuste o reemplazo. d. Participa y/o da soporte con monitoreo o emitiendo su opinión técnica en los proyectos de introducción de nuevos productos o durante modificaciones o reparaciones en el cuarto de producción. 10. Responsable del control de análisis relacionados con análisis físico-químicos. 11. Preparación de las soluciones necesarias para sus actividades. 12. 13. Responsable del control de análisis relacionados con medios de cultivo y equipos de laboratorio. Seguimiento a los controles de calidad de los equipo, reactivos y medios de cultivo del laboratorio de calidad. 14. Ejecución de actividades relacionadas con la validación de equipos y métodos de laboratorio. Soporte a validaciones de cuartos limpios y sistemas críticos. 15. Responsable de entender y contribuir con el mejoramiento de los procedimientos locales (SOP); así como cumplir con los requisitos de las especificaciones divisionales. 16. Contribuir con el proceso de mejora y resolución de oportunidades del área. 17. Contribuir con la administración del inventario de los reactivos y suministros del área de Microbiología. 18. Aplicar y seguir los lineamientos de EHS de acuerdo a los procedimientos establecidos, estándares y normas oficiales mexicanas. 19. Usar el equipo de protección asignado y cumplir con lo establecido en el punto seis de la NOM-017.
Puestos Supervisados:
N/A
Designación de suplencia (Aplica para, Dirección, Gerencia y Superintendencia):
N/A
Escolaridad:
Carrera profesional en las áreas de Ingeniería del Medio Ambiente, Bioquímica, QFB o disciplinas similares.
Experiencia:
· 1-3 años de experiencia probada en el campo o área afín.
· Experiencia en materia de ambiente controlado.
Conocimientos:
· Comprensión escrita del idioma inglés. Interpretación de documentos en inglés
· Conocimientos de Sistema de Calidad ISO 13485, FDA, QSR.
· MDSAP (Medical Device Single Audit Program).
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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