QUALITY SYSTEMS ENGINEER
Descripción de la oferta de empleo
Se convertirá en una de las personas de referencia en el apartado de Compliance en relación con todas las regulaciones y estándares del sector, un nicho específico de la industria farmacéutica.
Responsabilidades.
Desarrollo de sistemas de Calidad y Gestión Documental.
Soporte a Registros Internacionales.
Evaluación de impacto en el uso de las herramientas vinculadas al área.
Responsable de la unidad de Control de Cambios y buenas prácticas.
Mejora continua de los procedimientos de Calidad y su integración en SAP.
Auditorías externas e internas.
Punto de referencia en materia normativa y regulatoria.
Requisitos.
Bachelor's degree in Chemistry, Biotechnology or other Sciences.
Al menos 3 años de experiencia en el área de Calidad dentro de la Industria Farmacéutica.
Valorable Máster relacionado con Gestión Documental.
Valorable SAP.
La empresa ofrece un proyecto indefinido, estable, con recorrido profesional y condiciones laborales y económicas competitivas.
Será fundamental, desde el punto de vista personal, que el candidato demuestre pasión por su trabajo, compromiso y liderazgo.
Detalles de la oferta
- Fyte
- Sin especificar
- 18/10/2024
- 16/01/2025
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