Descripción y detalle de las actividades
This position executes and coordinates Quality Engineering functions for the organization in sterile and non sterile processes. The position requires a dynamic, hard-working quality professional with a desire to work for a fast-paced, large corporate organization. In addition to exceptional communication skills, a "roll-up" your sleeves" entrepreneurial attitude is expected. Lead and coordinate Corrective and Preventive Actions (CAPA) for Customer complaints, and process non-conformities. Develop and define measurement equipment and test methods to evaluate and perform component or process inspections. Define effective control plans for warehouse to operations delivery of raw materials' processes. Define, and lead continuous improvement projects focused on quality improvement, and cost reductions. Perform periodic audits of the accuracy and cleanliness of component storage locations and communicate results with appropriate warehouse personnel. Support the implementation and improvements for Good Manufacturing Practices (GMPs). Serve as an ISO-13485 Lead Internal Auditor, participating in the Internal Audit Program. Ensure compliance with domestic and international regulations associated with product lines and processes
Experiência y requisitos
Industrial, Electrical, etc 3-5 years of Quality Control/Engineering experience Medical Devices Experience (pharmaceutical, food or personal Care Supervisory experience desire Internal / Lead Auditor ISO 13485:2016 MDSAP knowledge / experience Office Windows: Word, Excel, Power Point, etc. Strong leadership Effective communication Management skills / Decision Making Six Sigma (BB/GB) Lean Manufacturing Experience
**Número de vacantes** 1
**Área** Calidad
**Contrato** Permanente
**Modalidad** Presencial
**Turno** Diurno
**Jornada** Tiempo Completo
**Horario** Lunes a viernes de 8:00 am a 5:00 pm
**Estudios** Carrera Profesional
**Inglés **Hablado: 90%, Escrito: 90%
**Sexo** Indistinto
**Disponibilidad p. viajar** No