Mexicali, Baja California- 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
- Lead multidisciplinary teams in order to accomplish moderate to high complexity task/projects
Experiencia y requisitos
- B.S. in Mechanical Engineering, Electrical Engineering, Manufacturing or Industrial Engineering
- Advanced English
- + 3 years as a Process Engineer in the medical, aerospace, or automotive sector.
- 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 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