Manufacturing Improvement Engineer | Project Lead

Zvh; Tijuana; On-site; MXN 600,000 - 800,000; Full time

Job summary

Baxter in Mexico is seeking a Mechanical Manufacturing professional to help integrate and improve device manufacturing processes. You will lead significant projects, manage timelines and budgets, and drive cost quality improvements across operations.

The role requires five years of related experience in ISO/FDA-regulated environments, strong problem-solving and project-management skills, and advanced English abilities. This position is based in Tijuana.

Qualifications

• Bachelor's degree in an engineering field is required.
• Minimum of five years of related experience.
• Experience in ISO/FDA-regulated environments and GMP requirements.
• Experience writing and executing process validations (IQ/SV/DOE/OQ/PQ).
• Advanced English communication skills.

Responsibilities

• Lead Margin Improvement Projects (MIP) per the plant plan and departmental commitments.
• Ensure timely implementation of projects without impacting manufacturing lines.
• Identify opportunities for MIP projects through ideas related to direct materials and validate savings.
• Collaborate with Procurement for quotations and feasibility assessments.
• Lead Workshops, Kaizen, and VAVE events for MIP ideas with cross-functional teams.
• Lead project planning including scheduling, costs, and resources.
• Develop and complete process validation activities (IQ/SV/OQ/PQ/TMV) per SOPs and GMP.

Skills

Lean practices

Six Sigma

Project management

Leadership

Problem solving

Cross-functional collaboration

Education

Bachelor's degree in Mechanical / Mechatronics / Electrical / Electromechanical / Systems Engineering or related field

Tools

IQ/SV/OQ/PQ

Job description

Baxter in Mexico is seeking a Mechanical Manufacturing professional to help integrate and improve device manufacturing processes. You will lead significant projects, manage timelines and budgets, and drive cost quality improvements across operations.

The role requires five years of related experience in ISO/FDA-regulated environments, strong problem-solving and project-management skills, and advanced English abilities. This position is based in Tijuana.