Quality Engineer Ii Or Iii

Descripción y detalle de las actividades

Experiência y requisitos
- ISO 13485 - Medical Devices Quality Management System (QMS) (ISO 13485 Change Control Program & ISO 13485 CAPA Program) -ISO 11607 (Packaging for terminally sterilized medical devices) -ISO 14971 (Application of risk management to medical devices) -Implementing/maintaining AQL -Six-Sigma Green Belt / Black Belt -Bi-lingual in English and Spanish

**Número de vacantes** 1

**Área** Calidad

**Contrato** Permanente

**Modalidad** Presencial

**Turno** Diurno

**Jornada** Tiempo Completo

**Estudios** Especialidades Diplomados

**Inglés **Hablado: 90%, Escrito: 90%

**Sexo** Indistinto

**Disponibilidad p. viajar** Si