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
· 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
• B.S. in Mechanical Engineering, Electrical Engineering, Manufacturing or Industrial Engineering
• Technical experience working in high-volume manufacturing environment.
• 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.
• Good Spanish and English communication skills, both verbal and written, and the ability to effectively interface
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 Si