Incoming Inspection Quality Engineer

Descripción y detalle de las actividadesDuties include execution of all Incoming quality-related activities. This includes but is not limited to Quality System; Quality Engineering functions; Inspection activities, Gage Calibration and Document Control. Responsible for all Documentation Control activities associated with Quality System requirements, including Device History Records (DHR), Mexico Processes, employee training records, validations, and other Quality Records. Responsible for ongoing adherence to external regulations as required by the Food and Drug Administration GMP, ISO 13485 and other applicable regulations. Reviews and approves changes to local or external InstructionsExperiência y requisitosEngineering degree3 Years minimum experience as an Incoming/Receiving Quality Engineer in a Medical Device Manufacturing companyKnowledge in the following fields:ISO13485Incoming InspectionInternal and supplier auditsProduct transfersProblem solving techniques (5whys, 8Ds, Ishikawa, DMAIC)OrganizaciónDemant Operations, S.A. de C.V.Correo de contactoGiroManufactureraActividad principalManufactura de aparatos auditivosNúmero de empleados400/**Área** Calidad**Contrato** Permanente**Turno** Diurno**Jornada** Tiempo Completo**Estudios** Carrera Profesional**Sexo** Indistinto