Mexicali, Baja California- Beneficios Superiores a LFT
Correo de contacto
*****@masimo.com
Giro
Maquiladora (Export.)
Actividad principal
Ensamble de sensores para oximetros (productos médicos).
Número de empleados
4350
Sitio Web corporativo
Aviso de privacidad
Descripción y detalle de las actividades
• Lead multidisciplinary teams in order to accomplish moderate to high complexity task/projects
• Becomes process expert of all process and equipment in the production area.
• Creates and maintains process work instructions associated with all manufacturing processes such as manufacturing assembly and in-process acceptance procedures.
• Develop and Implement Visual Aids and Physical Samples on critical steps of the process to indicate proper acceptance criteria.
• Trains manufacturing staff to released work instructions.
• Specifies, procures, installs, and validates manual, semi-automated and fully automated equipment.
• Develops and execute Process Validation Protocols or/and Transference Plans and generates test reports.
• Creates and maintains process risk assessments, PFMEA.
• Supports investigation, disposition, and corrective action of non-conforming materials.
• Establishes statistical process controls (SPC) for manufacturing operations.
• Develops and maintains World Class Manufacturing practices to ensure capability for the company’s products.
• Develops and implements cost reduction/process improvement programs
Experiencia y requisitos
- Bachelor degree in Mechanical Engineering, Electrical Engineering, Manufacturing or Industrial Engineering
- Advanced English (Essential for communication in English with corporate staff)
- Over 5 years of experience in process engineering in the industrial sector
- Visa B1 (Travel to the United States for process transfers)
- Experience in application of statistical process controls in a manufacturing environment
- Experience in manual, semi-automated and automation processes, verification and validation
- Hands-on skills with electro-mechanical troubleshooting and diagnostics
- Excellent technical writing abilities
- Excellent conceptual, analytical, and problem-solving abilities.
- Excellent computer skills - CAD, word processing, and spreadsheets.
- Ability to be part of a team and adept in building and leading teams.
- Knowledge and experience in FDA QSR requirements and preferably ISO-13485 requirements.
- Experience with planning and executing process validations and managing process risk assessment.
- Knowledge on developing and executing saving projects thought lean manufacturing techniques
Beneficios
Número de vacantes 1
Área Ingeniería
Contrato Permanente
Modalidad Presencial
Turno Diurno
Jornada Tiempo Completo
Horario
- Monday to friday 08:00-17:30 hrs
Estudios Carrera con título profesional
Inglés Hablado: Avanzado, Escrito: Avanzado
Disponibilidad p. viajar Si