Descripción y detalle de las actividades
experiência y requisitos
- bachelor degree in engineering (industrial, electronic, mechanical, electrical, mechatronic, bio). -must have at least 3-5 years’ experience in supervision of manufacturing assembly lines (medical devices and or electronic devices). -must be able to take the lead role, especially when conducting production meeting and interaction with engineering, planning, qa and r&d. -perform capacity analysis and generate reports in response to questions regarding production scheduling. -lead production meetings regarding performance metrics, floor training and qit. Knowledgeable in line clearances and compliance as it relates to fda cfr's for medical devices. -attainment and understanding of production schedules, material handling and lean manufacturing. Experience with erp systems (i.e. Dataflo), ms access, word and excel. Desirable: -apics certification. -preferred experience in a lean manufacturing environment. Preferred within a fda regulated (medical device) environment. -preferred experience with any type soldering/welding assembly.
Organización
sonova
correo de contacto
giro
manufacturera
actividad principal
proveedor de soluciones de cuidado auditivo - dispositivos médicos
número de empleados
800
aviso de privacidad
- /mexico/es/politica-de-privacidad-de-la-web-y-cookies*área* operaciones
*contrato* permanente
*turno* diurno
*jornada* tiempo completo
*estudios* carrera profesional
*inglés *hablado: 75%, escrito: 75%
*sexo* indistinto