Quality Inspector I

hace 2 semanas

Alajuela, Alajuela, Costa Rica Abbott Laboratories A tiempo completo

_MAIN RESPONSABILITIES_:

Responsable del cumplimiento de las politlcas y procedimienlos corporativos y divisionales aplicables.

  • Revisar la calidad del material, Los equipos y Los sistemas mediante la inspecci6n, medicion o prueba de materias primas, componentes, subensamblaje, ensamblaje final, empaque, etiquetado y documentaci6n.
  • Ayudar con las pruebas de validacion como se define en los protocolos de validacion con orientacion de ingenieria.

Asegurarse que toda la documentacion de evidenc:
ia cumpla con los procedimientos.

  • Auditar y verificar procesos como la auditoria de Linea y ambiental para evitar impacto en el sistema de calidad y de manufactura.
  • Revisar y verificar el cumplimiento de la documentacion, como registros de lotes, informes de materiales no conformes y registros de inspeccion.
  • Notificar al supervisor de problemas o errores, proporcionando una respuesta inmediata.
  • Contribuir a la ejecucion de pruebas cuando lo requiere el Supervisor de calidad o el lngeniero de calidad.
- ldentificar y segregar material no conforme de acuerdo con los documentos. Se coordina con el ingeniero de calidad para preparar y manejar el material dentro y fuera del area de cuarentena designada.
- lngresar datos a Los sistemas requer1dos. El uso de CATSWeb se limita a ejecutar consultas y / o lotes de entrada, datos de prueba.

  • Puede apoyar actividades de capacitacion de otros tecnicos de calidad.
  • Proporciona ideas para mejorar en areas coma la calidad, la productividad y la seguridad.
  • Aplica el conocimiento adquirido de procedimientos y practicas y una comprension completa de los fundamentos en un area funcional, y el conocimiento practico de otras disciplinas relacionadas. Realizara este trabajo en un entorno de sistema de calidad. El incumplimiento de las tareas adecuadas puede dar Lugar a incumplimiento de las regulaciones gubemamentales.
  • Realiza tareas generalmente en la naturaleza del entorno de fabricacion, que requieren trabajar de forma independiente o con supervision menor. Puede contribuir en el diseno, desarrollo o modificacion de procesos o procedimientos especificos del area. Se pueden asignar tareas adicionales con supervision de ingenieria y requeriran considerable juicio e iniciativa

_ Education_:

  • Bachillerato en Educacion Media concluido o algun tecnico

EXPERIENCE:

  • 02 Años de experiência en empresas de dispositivos médicos (Vascular unicamente)
  • Manejo de Office: word, excel, power point
  • Conocimiento básico de matemáticas, cálculos matemáticos

Otros:

Esta posición es para el Turno B

Puesto para el área de Receiving Inspection

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