Avent, S. de R.L. de C.V.

Project Coordinator

Avent, S. de R.L. de C.V.

Oct. 11

Tijuana, Baja California

Giro

Maquiladora (Export.)

Actividad principal

Manufactura de productos médicos

Número de empleados

800

Dirección

Noruega Edificio D-1B Parque Ind. La Mesa Tijuana, Baja California

Descripción y detalle de las actividades

Lead cross-functional team and plant resources to achieve on time and meeting goals of all the product introductions, changes, improvements, and required system maintenance activities affecting product lines specific to the assigned plant. Develop project plans and implementation programs, perform capacity/productivity analysis and cost estimations, and manage the project budget. Support the required systems for trial and commercialization activities (i.e. SAP, EtQ, Microsoft Excel), document the Bills of Materials, product specifications and drawings. Provide technical guidance for process optimization, for process validation and trial execution for Avanos product lines in the Tijuana facility. 1. Lead and execute all work in a safe and efficient manner. 2. Key contact for all plant-related project related topics and activities. 3. Develop and maintain project plan, project timing and implementation programs. 4. Properly and timely communicate to top management progress and escalate potential issues. 5. Assist in optimization of plant operations by executing on-going maintenance and/or changes to the bills of materials and providing insight into all roll-over plans. 6. Provide support which manages, maintains, and utilizes the SAP ERP system capability. 7. Record, analyze data, and submit accurate reports, plus maintain complete communications with project teams. 8. Develop solutions to assigned operational and process issues. Be an advocate for Six Sigma/LEAN manufacturing processes. Understand how to incorporate Six Sigma/Lean concepts to reduce waste and optimize manufacturing processes. 9. Be recognized as a plant expert for project insource validations, trials and commercialization activities. 10. Develop, publish, and communicate procedures, work instructions, forms, and process maps which allow consistent execution of required processes. 11. Assure ISO13485, FDA, Customs and other applicable regulation compliance rules are understood and applied as required for our processes. 12. Adhere to all applicable plant and Avanos Internal Controls.

Experiencia y requisitos

A Bachelor’s degree in engineering, science, logistics or a related discipline or equivalent professional experience. Five years of experience is desirable on similar position, particularly in the medical device, manufacturing industry and other highly regulated industry, with evidence of continued growth and successful leadership of Healthcare projects and programs. Experience in project transfers and new product introductions, demonstrated leadership in achieving results in a team environment.

Número de vacantes 1

Área Ingeniería

Contrato Permanente

Turno Diurno

Jornada Tiempo Completo

Horario L-J 7:30am-17:30pm Vier 7:30am-15:30pm

Estudios Titulo Profesional

Inglés Hablado: 90%, Escrito: 90%

Sexo Indistinto