Viant 482x100

Quality Inspector turno A lunes a viernes de 6:00 a.m. a 3:36 p.m.

Heredia, Costa Rica Sol. nº 4410
viernes, 3 de mayo de 2024

Main Purpose of Job: (Brief Summary)

  • Perform a variety of inspection duties for component specifications, assemblies and/or finished goods.  Use measuring devices and testing devices according to established engineering instructions or quality practice standards. Use manufacturing and quality assurance specifications to determine acceptance and/or performance. Additionally, inspect daily production and shipments to ensure it meets or exceeds the customer´s expectations. Work under moderate supervision. 

 

Main Job Duties/Responsibilities (List most important first)

  • Inspect and/or test parts, finished goods or re-worked items according to established specification and testing methods.
  • Document results and approve/reject items according to established standards.
  • Assure record accuracy for traceability according to established practices.
  • Monitor various manufacturing processes to assure component/product control, SOP and GMP control.
  • Perform data collection; interpret and analyze information to provide recommendations for solution.
  • Perform in process, pre-sterilization and post-sterilization testing; release conforming lots and document non-conforming lots.
  • Work within multi-functional teams, QA or cellular production and demonstrate a service attitude throughout the organization.
  • Perform production related computer transactions
  • Perform the final release of the product in the warehouse including: elaboration of the Certificate of Conformance (CofC), verification of the labels (product identification), verification of the packaging presentation of the product and the documentation related to be sure the compliance with the requirements prior to perform the shipping of the batches to the customers.
  • Perform the final release of the product in the warehouse including the verification of the labels (product identification), packaging and documentation related to be sure the compliance with the requirements prior to perform the shipping of the batches to the customers

 

Knowledge / Education

  • High school diploma desirable
  • Knowledge on ISO 13485 and Knowledge on CRF 820 CGMPs is a Plus

 

 

Viant es un proveedor global de servicios de diseño y fabricación de dispositivos médicos que se asocia e innova con los clientes para proporcionar la más alta calidad, dispositivos médicos que mejoran la vida de las personas. Hacemos esto a través de nuestra profundidad y amplitud de capacidades, integración de extremo a extremo, experiencia técnica y enfoque implacable en nuestros clientes y en la excelencia operativa. Con casi 6.000 asociados en 24 ubicaciones en todo el mundo, ofrecemos una combinación única de servicio y atención a pequeñas empresas con recursos de grandes empresas. Para más información, visite viantmedical.com o síganos en LinkedIn.
 
Viant proporciona igualdad de oportunidades de empleo (EEO) a todos los empleados y solicitantes de empleo sin tener en cuenta la raza, color, religión, género, orientación sexual,  nacionalidad, edad, discapacidad, estado civil, amnistía, o estatus como veterano cubierto de acuerdo con las leyes federales, estatales y locales aplicables. Viant cumple con las leyes estatales y locales aplicables que rigen la no discriminación en el empleo en todos los lugares en los que la empresa tiene instalaciones.

Otros detalles

  • Grupo de puestos Costa Rica
  • Función del puesto Quality Inspector
  • Tipo de pago Por hora
Location on Google Maps
  • Heredia, Costa Rica