Resumen del Puesto: This role involves leading multidisciplinary teams, becoming a process expert, creating and maintaining work instructions, and developing and implementing process improvements in a manufacturing environment. Puntos Destacados: 1. Lead multidisciplinary teams on complex tasks/projects 2. Become a process expert for all production processes and equipment 3. Develop and implement cost reduction and process improvement programs 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 * Beneficios Superiores a LFT **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