Sr. Process Engineer Design

hace 3 semanas


Mexicali, México Emprego MX A tiempo completo

Descripción y detalle de las actividades

Process improvement using Lean baselines, identification of main process KPIs, monitors and develop problem solvings in order to prevent and/or correct process issues. Will work on providing technical support for on-going production activities and participation in the development, assessment, deployment and monitoring of new products and processes. Develop and execute structured test plans to assess impact of modified or new processes. Collaborate with the corresponding key stakeholders in designing, validation, and executing process & software. Will align and prioritize along with Operations Managers, the productivity improvement projects, Standard Times measure and control, standard work, Quality Improvement projects implementation and other initiatives that supports an efficient use of resources. Research, develop and implement projects, while lead internal, and/or external cross-functional teams-based process development and improvement efforts. Implement and maintain control mechanisms and systems to follow up, measure the impact, and receive feedback of already implemented projects. Responsible for defining documentation, processing times and KPIs of new and existing processes. Investigate and propose new ideas, process and systems to improve companies KPIs related to operational cost. Use statistical tools, problem solving, lean manufacturing, and improvement continue tools as required and his/her regular duties. Control and Lead improvements task and activities among cross functional departments Provide coaching and feedback to the designers and Staff members on main indicators trends. Send weekly report on trends that are found during their interactions while reviewing design treatment plans, clinical investigations, Manufacturing issues, and complaints from customers. Responsible for planning, implementing, and managing compliance of internal quality processes in alignment with external, quality and regulatory standards requirements.

Experiência y requisitos

Bachelor's degree or internationally equivalent in Industrial Engineering, Quality engineering or other related fields Typically has 3-5 years of directly related experience Proficient in Microsoft Office Package Proficient in using Electronic Document Management Systems Experience in designing, execution, and measurement of quality processes Experience in investigation methodology and root cause analysis (5 Why’s, Fishbone etc.) Experience in statistical analysis methodology / data analysis Prior work experience in healthcare (FDA) regulated industry; biotech, pharma, medical device. Travel Estimated overnight travel is 10% Advanced level of English Speaking, Reading, and Writing. Strong effective oral and written communication skills with the ability to influence across the organization Advance knowledge in Microsoft office suite. Tableau Knowledge Ability to manage complexity and resolve conflicts that arise from balancing multiple priorities. Medical Device Regulatory Knowledge, ISO 13485, 21 CFR Part 820, ISO 14971 Lean Manufacturing knowledge for process mapping, analysis and improvement LEAN SIX SIGMA GREEN BELT

Organización

SDS de México, S. de R.L. de C.V.

Correo de contacto

Giro

Maquiladora (Export.)

Actividad principal

Industria de manufactura líder en la fabricación de instrumentos médicos dentales.

Número de empleados

3000

//**Área** Ingeniería

**Contrato** Permanente

**Turno** Diurno

**Jornada** Tiempo Completo

**Estudios** Titulo Profesional

**Sexo** Indistinto


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