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Automation Engineer
hace 1 semana
MARTECH MEDICALes una empresa ubicada en el parque industrial PIMSA I Mexicali, ofrece productos/servicios comocateter de plástico para uso médico,juego de cateter con accesorios,dilatador de plásticoy su principal actividad es fabricación de material desechable de uso médico.
Automation Engineer
**Requisitos**:
Carrera profesional concluida.
Contar con título y/o cédula profesional.
Experiência mínima de dos años en puestos similares.
Inglés avanzado-conversacional
Microsoft office (Excel, Word, Power point, outlook, etc.)
**Conocimientos**:
Maquinaria y equipo de producción
Validación de procesos IQ, CQ, PQ, TQ, etc.
Análisis de Riesgo y PFMEA
Automatización y sistemas de control para equipo de manufactura
Programación de PLC
Six Sigma, Lean Manufacturing
**Descripción general**:
Responsable de liderear iniciativas de automatización de procesos de manufactura para mejorar la eficiencia o reducir costos, incluyendo análisis financiero del proyecto.
Responsable de evaluar equipo nuevo para producción, transferencia de productos, validación de procesos, análisis y solución de problemas en producción y maquinaria.
**Responsabilidades principales**:
Velar por la seguridad y salud propia y de los demás cumpliendo con las medidas de prevención adoptadas, de acuerdo con su formación y con las instrucciones de la empresa.
Evaluar y definir factibilidad de proyectos de automatización en base a análisis financieros, técnicos y de resultados esperados.
Diseñar, desarrollar e implementar soluciones de automatización para cubrir necesidades de los departamentos de producción y soporte.
Identificar riesgos en los procesos, evaluarlos y/o mitigarlos, siguiendo los lineamientos de seguridad establecidos por la empresa.
Validar procesos de manufactura, instalar maquinaria, debido a transferencias, desarrollo de procesos de manufactura, mejoras en producción o cambios de ingeniería; escribiendo y ejercitando protocolos de validación y documentos relacionados (CP-1100,VA, IQ, OQ, PQ, TQ, SCR, PDHF, CCR).
Elaborar, actualizar e implementar documentación para control de procesos y calidad como SOP´s, SUP´s, QAP´s, WS, AMV´s, flijos de proceso, PFMEA´s, etc y/o cualquier documentación relacionada con la transferencia de productos y mejoras en producción.
Proveer entrenamiento al personal de producción, calidad y personal técnico según se requiera en procesos o procedimientos nuevos o como resultado de cambios en documentación.
Diseñar, desarrollar, fabricar y validar herramientas (TQ) para procesos nuevos o mejoras.
Investigar y desarrollar nuevas tecnologías de manufactura y automatización.
Comunicación con personal de otros departamentos, de la planta matriz y de otras compañías para la resolución de problemas.
**Ubicación**: Mercurio # 46 Parque Industrial Mexicali I, CP 21210
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