Medical Device Manufacturing Process Improvement Engineer

Zvh; Tijuana; Presencial; MXN 550.000 - 850.000; Jornada completa

Descripción de la vacante

Baxter is seeking a manufacturing engineer to integrate processes and drive continuous improvement across mechanical device manufacturing. You will lead Margin Improvement Projects, manage cross-functional teams, and ensure projects align with schedule, cost, and quality goals.

The role requires a Bachelor's in Mechanical Engineering, 5+ years' related experience, and strong English communication. ISO/FDA/GMP experience and process validation expertise are essential.

Formación

• Bachelor's degree in Mechanical Engineering or related field.
• Minimum 5 years of experience in a related position.
• Experience in problem-solving, project management and leadership, Lean practices, Six Sigma (preferred), and production line transfers.
• Experience working in ISO/FDA-regulated environments and under GMP requirements.
• Experience writing and executing process validations (IQ/SV/DOE/OQ/PQ).
• Advanced English proficiency, both written and verbal communication skills.

Responsabilidades

• Lead and manage Margin Improvement Projects (MIP) per plant plan and department commitments.
• Ensure timely and effective implementation of projects across manufacturing lines.
• Identify opportunities for MIP projects via self-initiated ideas for direct materials in device manufacturing.
• Collaborate with Procurement to manage quotations for evaluations of ideas.
• Lead Workshops, Kaizen, and VAVE events for MIP ideas with cross-functional teams.
• Develop and complete process validation activities per project plan and SOPs.

Conocimientos

Project management

Leadership

Lean practices

Six Sigma

Problem solving

Production line transfers

Educación

Bachelor's degree in Mechanical Engineering

Descripción del empleo

Baxter is seeking a manufacturing engineer to integrate processes and drive continuous improvement across mechanical device manufacturing. You will lead Margin Improvement Projects, manage cross-functional teams, and ensure projects align with schedule, cost, and quality goals.

The role requires a Bachelor's in Mechanical Engineering, 5+ years' related experience, and strong English communication. ISO/FDA/GMP experience and process validation expertise are essential.