**Descripción y detalle de las actividades**- Responsible to develop and implement changes to product design and/or to the manufacturing process to achieve significant quality, efficiency or cost improvements. This requires participation in new product development programs, identifying design-for-manufacturability issues and ensuring these issues are addressed prior to release.EXPERIENCE- Bachelor's Degree in Engineering (Mechanical, Electrical/Electronics, Industrial or relevant degree). 1 to 3 years - Manufacturing environment in medical industry. Advance English (required). Lean Manufacturing certification (preferred).**Experiência y requisitos**- Support validation program to ensure all molding equipment validations are carried out within specified time-frame. Provide support in the implementation of all changes affecting engineering for product line components. Support molding transfer projects to ensure a secure supply chain for a growing product line. Implement changes and complete operator training. May lead small scope projects under the direction and supervision of manager. Perform or facilitate all the required testing as specified in the molding protocol. Review, analyze and document test results in a molding test report. Participate as a team member on larger manufacturing projects and help lead projects with specific focus on small scope projects, as assigned by manager. Provide support on mold verification, sample process development, mold changes, and set-ups. Process observation, development, and documentation. Work closely with, and communicate with, all other production and support teams. Documents and communicates with Process Technicians, Process Engineers and Shift Supervisor results of problem solving and any deviations from established methods or procedures that may be necessary to resolve specific issues. Supports Process Engineers in development of process parameters and process improvements. Communicates effectively with leads, supervisors, machine operators and supporting departments (i.E. Purchasing and Quality). Complies with all local, state, federal and Haemonetics safety regulations, policies and procedures. Follows all applicable standard operating procedures, manufacturing instructions and/or standing instructions. Ability to work independently without supervision and with minimum direction. Must be willing to work other shifts or perform other duties/tasks that are of reasonable request by Management.**Organización**- Haemonetics México Manufacturing S. de R.L. de C.V.**Giro**- Maquiladora (Export.)**Actividad principal**- Líder global en el diseño y fabricacion de productos para la administración de sangre**Número de empleados**- 1200**Número de vacantes** 1**Área** Ingeniería**Contrato** Permanente**Turno** Variable**Jornada** Tiempo Completo**Estudios** Titulo Profesional**Sexo** Indistinto
