Manufacturing Eng Jr
hace 5 meses
**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.
**Principales Actividades, Responsabilidades y Autoridades**:
- Responsable de validaciones de primeros artículos (FAI)
- Actualización y/o creación de documentos
- Dar soporte a ejecuciones de validaciones (IQ/OQ/PQ/Pilot)
- Diseño y/o mejora de herramientas
- Soporte a transferencias de productos
- Cumplir sus funciones apegado a la cultura de cumplimiento de normas y prácticas de negocio éticas en la organización.
- Cumplir e impulsar el cumplimiento de las políticas de Baxter y el código de conducta.
- Implementar el código de conducta de Baxter, políticas y procedimientos, incluyendo, pero no limitado a la política Global de interacciones y política de terceros.
- Mantener la coordinación entre departamentos, para asegurar de manera ininterrumpida el flujo de trabajo.
- Apoyar en el desarrollo de nuevos productos desde la perspectiva de cada uno de los procesos tales como: manufactura, costura y ensamble.
- Participar en iniciativas de proyectos de mejora de la calidad en el producto y en los procesos de manufactura. Recomendar acciones preventivas y correctivas. Apoyar en la implementación de acciones correctivas en fallas del producto o proceso.
- Aplicar herramientas de mejora continua en producción, a través de metodología Lean y/o Six Sigma.
- Asegurar el cumplimiento de las medidas de seguridad y buenas prácticas en procesos de manufactura: reportar problemas relacionados al proceso y de seguridad, para asegurar el cumplimiento en todas las regulaciones.
- Apegarse a procesos de manufactura y calidad, así como asegurar el cumplimiento por parte de los operadores.
**Escolaridad**:
- Carrera en Ingenieria (Terminada o en proceso)
**Experiência**:
- Mínimo 1 - 2 años de experiência, trabajando directamente en procesos de manufactura (Industria Medica ISO13485 deseable).
**Conocimientos**:
- Conocimiento en técnicas de solución de problemas
- MS Office
- Inglés (Intermedio)
- Toma de tiempos
- Conocimientos de GD&T
- Conocimientos de CAD (AutoCad, Solidworks, Inventor, u otros)
- Conocimientos de Estadística
- Conocimiento en herramientas de manufactura esbelta
- Conocimientos sobre validación de procesos
- Conocimientos en buenas prácticas de documentación
**Competencias**:
- Comunicación.
- Enfoque en el cliente.
- Colaboración y Trabajo en Equipo.
- Pensamiento Crítico y Resolución de Problemas.
- Toma de decisiones.
**Atributos**:
- Entusiasmo por aprender y mejorar de forma continua.
- Responsabilidad personal sobre los resultados e integridad.
- Dedicación incondicional a la calidad
**Valores**:
- Integridad y Confianza.
- Ética Laboral.
- Honestidad Intelectual
**Reasonable Accommodations**
**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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