Número de empleados
Sitio Web corporativo
Descripción y detalle de las actividades
Accountable for integration of new and existing processes (via new product introduction and transfer from other Hillrom sites) and development and continuous improvement of manufacturing processes for Medical devices. May have complete project responsibility for significant projects within specialized area. •Apply experience, training and acquired engineering techniques to solve problems encountered in design, redesign or troubleshooting. •May supervise and/or give technical and safety direction or guidance to peers, technicians, designers, drafters, model makers and others. May serve as project leader. •Meet with external customers and suppliers to exchange information and to assist with more difficult technical problems. •Participate in project planning/direction of smaller projects or segments of large projects to include scheduling, monitoring costs, resources, workforce loading, etc., also ensure the correct execution of the activities related to the project. •Integration of existing processes (via transfer from other Welch Allyn sites) and development and continuous improvement of manufacturing processes for mechanical devices. •Design and implementation of production fixtures/tools and inspection equipment. •Capacity (equipment, labor, space) and maintenance planning and strategies creation. •Direct Support to operations for production yield, productivity, downtime tracking and corrective action. •Support and improve production lines using as a base lean manufacturing tools and continues improvement tools as SMED, TPM, Kaizen etc. •Coordination of activities related to manufacturing transfer to new manufacturing site (Previous experience) •Development and completion of process validation (IQ/OQ/PQ/TMV), while ensuring that changes made to specifications, methods, processes or procedures are verified or, where appropriate, validated according to standard operating procedures and QSR’s element 820.75, before implementation.
Experiencia y requisitos
• Mechanical Engineer, Mechatronic Engineer, Electrical Engineer, Electromechanic Engineer, Systems Engineer or similar. Experience: • 6 to 8 years’ experience on engineering field. Medical companies as a plus. • Experience in problem solving, project management, lean practices, six sigma, line transfers. Experience working in ISO / FDA regulated environments and GMP’s. • Strong background in development and completion of Process Validation (IQ,OQ &PQ). • Bilingual: Oral and written communications in English Intermediate.
Número de vacantes