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A quién buscamos:
Mejoradores de procesos orientados a detalles. Pensadores(as) críticos(as) que, naturalmente, ven oportunidades para desarrollar y optimizar procesos de trabajo, encontrando formas de simplificar, estandarizar y automatizar.
Gestores(as) de datos. Personas que disfrutan compilando, organizando y consolidando grandes volúmenes de datos e informes.
Documentadores meticulosos. Personas orientadas(os) a los detalles que disfrutan mantener una documentación meticulosa de informes, métricas, propuestas y presentaciones.
Traductores(as) de datos. Comunicadores altamente efectivos que pueden transformar los hallazgos de datos en recomendaciones para elaborar informes y presentaciones a nível ejecutivo.
Que Harás:
- Control de documentos.
- Seguimiento a las necesidades del área de regulatorios, ventas y licitaciones sobre la documentación legal de otros sitios filiales de Stryker.
- Soporte en el seguimiento de estrategias regulatorias locales y regionales.
- Comunicación con los sitios de manufactura para obtención de información vigente.
- Revisión de la información regulatoria para el desarrollo de productos a lo largo del ciclo de vida del producto dentro de la organización.
Que necesitas:
- Formación en Ingeniería Biomédica, Biotecnología, bioquímica, farmacia, o similares dentro del área de Ciencias de la Salud.
- Paquete office (Word, Excel)
- Deseable tener conocimiento del sistema JDE
- Tener conocimientos de inglés intermedios/avanzados
- Multitarea, resolución de problemas, organización, razonamiento lógico, enfocado en el detalle
