Manufacturing Engineer I: Process Transfer & Production

Baxter International Inc.; Tijuana; Presencial; MXN 320.000 - 400.000; Jornada completa

Descripción de la vacante

Baxter International Inc. in Mexico is seeking a Manufacturing Engineer I to help transfer and improve mechanical device manufacturing processes. You will oversee projects, optimize workflows, coordinate with Baxter sites, and implement fixtures, tools, and inspection equipment.

The role emphasizes problem solving, project leadership, lean practices, and strong English communication in ISO/FDA GMP environments, with potential cross-site collaboration and CAPA involvement.

Formación

• Minimum one year of experience in a related position.
• Experience in problem solving, project management, lean practices, six sigma, line transfers.
• Experience working in ISO / FDA supervised environments and GMP's.
• Bilingual: Oral and written communication in English required.

Responsabilidades

• Apply engineering techniques to tackle build, redesign or repair problems.
• Supervise and mentor peers; may serve as project leader.
• Meet with external suppliers to exchange information and solve technical problems.
• Plan projects, manage costs, resources and scheduling for large initiatives.
• Integrate existing processes and develop manufacturing processes for mechanical equipment.
• Build production fixtures/tools and inspection equipment as needed.
• Plan capacity, maintenance and production yield improvements.
• Coordinate transfer activities to new manufacturing sites.
• Develop process instructions, routers and bill of materials.

Conocimientos

Mechanical Engineer

Mechatronic Engineer

Electrical Engineer

Electromechanics Engineer

Systems Engineer

Bilingual English

Problem solving

Project management

Lean practices

Six Sigma

ISO 13485

FDA GMP experience

Descripción del empleo

Baxter International Inc. in Mexico is seeking a Manufacturing Engineer I to help transfer and improve mechanical device manufacturing processes. You will oversee projects, optimize workflows, coordinate with Baxter sites, and implement fixtures, tools, and inspection equipment.

The role emphasizes problem solving, project leadership, lean practices, and strong English communication in ISO/FDA GMP environments, with potential cross-site collaboration and CAPA involvement.