Quality Technician III

16 hours ago

Costa Rica, India BOSTON SCIENTIFIC Full time US$ 6,00,000 - US$ 12,00,000 per year
Job Description

Quality Technician III - Shift A Cartago

Fecha: 22 oct. 2025
Ubicacin: Zona Franca La Lima, Cartago, CR
Empresa: Boston Scientific

Diversidad - Innovacin - Preocupacin - Colaboracin global - Espritu ganador - Preocupacin - Alto rendimiento

En Boston Scientific, le brindaremos la oportunidad de aprovechar todo lo que hay dentro de usted trabajando en equipos de empleados diversos y de alto rendimiento, abordando algunos de los desafos ms importantes de la industria de la salud. Con acceso a las ltimas herramientas, informacin y capacitacin, lo ayudaremos a mejorar sus habilidades y su carrera. Aqu, recibir apoyo para progresar, sean cuales sean sus ambiciones.

Sobre el Rol:

Brindar apoyo al departamento de Calidad en las reas de Quejas, Recepcin, Liberacin de Calidad y Aseguramiento de la Calidad.

Sus responsabilidades incluyen:
  • Realizar pruebas asociadas con las pruebas de productos.
  • Participar y seguir instrucciones con respecto al anlisis estadstico bsico.
  • Asistir a los ingenieros en el anlisis de fallas y actividades CAPA.
  • Participar en proyectos de mejora continua.
  • Asistir con problemas de calidad y actividades relacionadas con mtricas de calidad.
  • Ayudar con el anlisis de fallas del producto.
  • Realizar pruebas, recopilar datos y analizar los resultados de las pruebas de productos y la supervisin de procesos.
  • Ayudar con las actividades relacionadas con la auditora.
  • Asistir en la creacin, validacin y mantenimiento de archivos y formularios de datos.
  • Utilizar sistemas de documentacin para buscar informacin y generar solicitudes de cambio.
  • Asistir en el desarrollo y calificacin de mtodos de prueba, hojas de datos, accesorios de prueba y equipos de prueba.
  • Asistir en la investigacin y disposicin de materiales, diseos y/o sistemas no conformes.
  • Revisar los registros del historial del dispositivo (DHR) y los registros de aceptacin para asegurarse de que todas las actividades en el Registro maestro del dispositivo (DMR) se hayan realizado y aprobado.
  • Actualizar las bases de datos y las hojas de clculo utilizadas para rastrear, monitorear e informar las actividades del departamento.
Qu buscamos?
  • Al menos 3 aos de experiencia en puestos similares.
Requisitos:
  • Bachillerato en Educacin Media concluido (requisito indispensable).
  • Nivel tcnico requerido: Calidad, Produccin o Metrologa (requisito indispensable).
  • Deseable: estudiante de al menos 50 PERCENT de alguna carrera universitaria afin.
  • Disponibilidad para laborar en Turno A (Lunes a Viernes de 6:00 a.m. a 3:30 p.m.)
  • Deseable: Nivel de ingls 70 PERCENT .
  • Deseable: Conocimiento en SAP y MES.

#CTGTA
Nmero de la requisicin: 616312

Como lder en ciencia mdica durante ms de 40 aos, estamos comprometidos a resolver los desafos que ms importan, unidos por un profundo cuidado por la vida humana. Nuestra misin de promover la ciencia de por vida consiste en transformar vidas a travs de soluciones mdicas innovadoras que mejoran la vida de los pacientes, crean valor para nuestros clientes y apoyan a nuestros empleados y las comunidades en las que operamos. Ahora ms que nunca, tenemos la responsabilidad de aplicar esos valores a todo lo que hacemos, como empresa global y como ciudadano corporativo global.

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