Corporate Quality Auditor at Grifols ensuring compliance with Good Manufacturing Practices and internal policies. Assessing quality across pharma and medical device manufacturing sites.
Responsibilities
Recoger los documentos necesarios para preparar las auditorías.
Definir la agenda de la auditoría.
Preparar los documentos asociados a la auditoría, antes de que se realice (lista de verificación, hojas de trabajo, etc).
Realizar las Auditorías de Calidad Corporativa, asegurando que se cumpla el plan de auditoría establecido en la agenda.
Escribir el Informe de Auditoría con las actividades relevantes realizadas en la empresa auditada, identificando los riesgos y oportunidades de mejora, de manera oportuna.
Clasificar las conclusiones y redactar recomendaciones.
Revisar las acciones correctivas y preventivas derivadas de la auditoría.
Apoyar la gestión de indicadores del área.
Requirements
Tienes un grado en Ciencias de la Vida (Farmacia, Biología, Química, Biotecnología,…) o un Grado en Ingeniería (Química o Industrial).
Tienes de 3 a 5 años de experiencia en GMP dentro de la industria farmacéutica/dispositivos médicos/productos estériles.
Muy valioso tener experiencia en Auditorías y/o Validaciones.
Tienes un alto conocimiento demostrado de GMP.
Tu inglés es avanzado.
Estás disponible para viajar (aproximadamente un 30%).
Benefits
Flexibilidad para trabajo híbrido
Horario flexible: de lunes a jueves de 7-10 a 16-19h y viernes de 8-15h
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