- Beneficios de acuerdo a la LFT
Giro
Maquiladora (Export.)
Actividad principal
Empresa de nivel internacional dedicada al ensamble de baterías para distintos componentes.
Número de empleados
300
Sitio Web corporativo
Descripción y detalle de las actividades
Job Objective:
Ensure consistent quality of products and processes through the establishment and enforcement of quality standards, including the testing of materials and products. Responsible for overseeing suppliers’ daily quality performance, preparing quality reports, and implementing corrective action programs. Develops and maintains process controls to support quality improvement and compliance with company standards, including ISO 9001, ISO 13485, and FDA QMSR regulations.
This position is essential to ensure that the processes defined for product manufacturing incorporate all necessary quality requirements. The role works closely with the Purchasing department regarding materials and assists in supplier selection from a quality perspective when required.
Complies with the applicable requirements of the Quality and Environmental Management System.
Experiencia y requisitos
Education Background (Major, Degree etc.) / Bachelor's degree or 5 years (Mechanical or Electronic Engineer is a plus) of equivalent work experience.
Work Experience (Area, Service Year etc.) / A minimum of 3 years of experience as a quality engineer, the fundamental knowledge of electronics, plastics and assembly processes (medical or electronic industry is preferable) of battery components is an advantage. Experience in FMEA development, working with 5S, gage R&R, CPK studies and implementing SPC
Language (Level) / Advanced (Reading and Writing that allow fluid presentations of Projects and / or Participation in Negotiation Processes
Computational knowledge / Use of software packages such as Microsoft Office, Minitab and specialized test equipment
Competencies / Must be able to communicate effectively at all levels and have demonstrated skill in technical writing.
Additional comments / ASQC and Six Sigma certification a plus. (experience with FDA REGULATIONS, ISO-13485 or ISO9001). Actively participate in the manufacturing process, some travel to customers, suppliers, others.
Beneficios
Número de vacantes 1
Área Ingeniería
Contrato Permanente
Modalidad Presencial
Turno Diurno
Jornada Tiempo Completo
Estudios Carrera con título profesional
Inglés Hablado: Avanzado, Escrito: Avanzado
Disponibilidad p. viajar No
