Specialist Regulatory Affairs

hace 4 semanas


Bogota, Colombia Abbott Laboratories A tiempo completo

**RA Specialist**

**Acerca de Abbott**

Abbott es líder mundial en cuidado de la salud, que crea ciencia innovadora para mejorar la salud de las personas. Siempre estamos mirando hacia el futuro, anticipando cambios en la ciencia y la tecnología médica.

**Trabajando en Abbott**

En Abbott, puedes hacer un trabajo que importa, crecer y aprender, cuidar de ti mismo y de tu familia, ser verdaderamente quien eres y vivir una vida plena. Tendrás acceso a:

- Desarrollo profesional con una empresa internacional donde podrás hacer crecer la carrera que sueñas.
- Una compañía reconocida como mejor lugar para trabajar en docenas de países alrededor del mundo y nombrada una de las empresas más admiradas del mundo por Fortune.
- Una compañía que es reconocida como una de las mejores compañías grandes para trabajar, así como un mejor lugar para trabajar para la diversidad, las madres trabajadoras, mujeres ejecutivas y científicas.

**La Oportunidad**

Esta posición está ubicada en Bogotá en nuestra división de Core Diagnostics.

Estamos potenciando la toma de decisiones médicas y económicas más inteligentes para ayudar a transformar la manera en que las personas manejan su salud en todas las etapas de la vida. Cada día, se realizan más de 10 millones de pruebas con los instrumentos de diagnóstico de Abbott, proporcionando resultados de laboratorio para millones de personas.

Como **RA Specialist**, tendrás la oportunidad de dar soporte en temas regulatorios sanitarios relacionados con reactivos y dispositivos médicos a otras áreas de la División y de la Afiliada. Asimismo, te encargarás de asegurar el mantenimiento de los sistemas de control establecidas por la división para controlar los procesos de evaluación, sometimiento y aprobación de registros sanitarios.

**Que harás**
- Apoyar la elaboración de expedientes para registro sanitario y seguimiento de trámites con el INVIMA dando cumplimiento a la normativa vigente y las políticas de Abbott.
- Evaluar el impacto de las notificaciones de cambios (NTC) y encuestas (Survey) de los productos del portafolio y programar los tramites aplicables de acuerdo con análisis realizado.
- Asegurar el archivo y control de documentos legales y técnicos requeridos para el mantenimiento de los registros sanitarios.
- Dar soporte a las Divisiones de Molecular y Transfusión en el trámite de obtención de registros sanitarios y aprobación de productos para su comercialización.

**Cualificaciones requeridas**

1. Profesional en Química Farmacéutica o Bacteriología

2. Habilidad de trabajo bajo presión, gestión de múltiples prioridades al mismo tiempo, capacidad de análisis, capacidad de resolución de problemas, enfoque al detalle, comunicación asertiva.

**Cualificaciones preferidas**

1 a 5 años de experiência en asuntos regulatorios de reactivos, dispositivos o medicamentos.

Aplicar ahora

Sigue tus aspiraciones profesionales con Abbott para obtener diversas oportunidades con una empresa que puede ayudarte a construir tu futuro y vivir tu mejor vida. Abbott es un empleador de igualdad de oportunidades, comprometido con la diversidad de los empleados.



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