Organización
Giro
Maquiladora (Export.)
Actividad principal
Manufactura de dispositivos medicos diversos.
Número de empleados
700
Sitio Web corporativo
Sitio Web
Descripción y detalle de las actividades
Partnering with production manager how to comply with the production schedules. Knowledge how to process a Devices History Record for the products (DHR) and assures proper completion. Comply with the internal HR guidelines and HSE department. Ensures that finished product orders are captured in SAP system. Responsible of coordination the activity in production plans and/or accomplish the goals of the production area and the plant. Assure the accomplish to production standards and quality (ISO 13485, QSR 820). Ensure compliance with good manufacturing practices Manages his crew has been receive the properly training. Reviews the production schedules and estimates the man-power to complete the assigned work orders. Signs and review scrap reports and ensures that the amount to be discarded is correct. Perform daily reports to visualize the progress of production plans. Elaborates work orders necessary for the maintenance department to meet the specific needs of the production area. Uses lean tools to identify improvements to the processes under his responsibility. Responsible for the coordination and veracity of inventories in their responsibility areas. Maintains the correct production line balance defined by the manufacturing engineer. Manages human resources, changes of area and / or shift, promotions, removals, disciplinary measures, scheduling of vacations and authorization of permits. Responsible for providing human resources all the necessary information for the appropriate and timely preparation of the pre-payroll of the personnel in charge. Participates in the activities of the company as required (monthly inventory, annual physical inventory, training courses, safety and hygiene commission). Responsible for promoting the values of the company through its example, training and promotion programs, and participates with the human resources department in motivation programs.
Experiencia y requisitos
3 Years of Experience as Production Supervisor Proven experience working in Medical devices company Knowledge of ISO Standard 13085 Good English Skills Able to travel (25% @ beginning) Bachelor of engineering or truncated career. Experience on apply Lean Tools on production process Valid Visa able to work in Tecate. Team Player Results Oriented Please send your resume to reclutamiento_tecate@teleflex.com specify the position that you have applied.
Número de vacantes
1
Área
Producción
Contrato
Permanente
Turno
Diurno
Jornada
Tiempo Completo
Horario
Lunes a Viernes 7:00 - 5:00 P.M.
Estudios
Carrera Profesional
Inglés
Hablado: 90%, Escrito: 90%
Sexo
Indistinto