Engineer, Manufacturing Jr

Baxter healthcare - welch allyn de mexico, s. de r. l. de c. v. - Baja California
hace 30+ días (14/05/2024)

descripción del empleo

Accountable for integration of existing processes (via transfer from other Welch Allyn sites) and development and continuous improvement of manufacturing processes for mechanical 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 and may direct portions of smaller projects or segments of large projects to include scheduling, monitoring costs, resources, workforce loading, etc - 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 as required. - Capacity (equipment, labor, space) and maintenance planning and strategies.Production yield, productivity, downtime tracking and corrective action. - Coordination of activities related to manufacturing transfer to new manufacturing site. - Development and completion of process validation, 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. - May lead or participate with organizational and group operations’ management in CAPA activities by conducting, determining and verifying corrective actions necessary to ensure continued compliance with division policy and procedures, Federal regulations under Title 21 CFR Part 820, and ISO 13485:
2003. - Responsible for monitoring, identifying tendencies, investigating and solving problems related to manufacturing processes. -

Education required:
- Electronics engineer.Desirable Experience:
- Minimum one year of experience in a related position. - Oral and written communication skills in English and Spanish. - Experience in problem solving, project management desirable, lean practices, six sigma desirable, line transfers desirable. Experience working in ISO / FDA regulated environments and GMP’s, desirable.Unete a nuestro Equipo de Trabajo, envia tu CV a Joel Mercado, [email protected]


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