Manufacturing Improvement Engineer — Medical Devices

Baxter International Inc.

Tijuana

On-site

MXN 600,000 - 1,000,000

Full time

24 hours ago
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Job summary

Baxter International Inc. in Mexico seeks an experienced Mechanical/Manufacturing engineer to lead integration and improvement of device manufacturing processes. You will oversee projects from concept to validation, ensuring timeline, cost, and quality targets are met.

The role emphasizes cross-functional collaboration, process validation (IQ/SV/OQ/PQ/TMV), and implementing Lean and Six Sigma approaches in ISO/FDA-regulated GMP settings. Fluency in English is required.

Qualifications

  • Bachelor's degree in Mechanical Engineering or related field.
  • Minimum 5 years of related experience in manufacturing/engineering.
  • Experience in ISO/FDA-regulated environments and GMP requirements.
  • Strong problem-solving and leadership skills.
  • Advanced English proficiency, written and spoken.

Responsibilities

  • Lead integration of existing processes and development of manufacturing processes.
  • Manage projects from concept to validation within timelines and budget.
  • Identify opportunities for Margin Improvement Projects (MIP) and cost savings.
  • Collaborate with Procurement for quotations and feasibility assessments.
  • Lead workshops and Kaizen events related to process improvement.
  • Develop and complete IQ/SV/OQ/PQ/TMV validation activities and update SOPs accordingly.

Skills

Project management
Lean practices
Six Sigma
GMP environments
Process validation

Education

Bachelor's degree in Mechanical Engineering

Job description

Baxter International Inc. in Mexico seeks an experienced Mechanical/Manufacturing engineer to lead integration and improvement of device manufacturing processes. You will oversee projects from concept to validation, ensuring timeline, cost, and quality targets are met.

The role emphasizes cross-functional collaboration, process validation (IQ/SV/OQ/PQ/TMV), and implementing Lean and Six Sigma approaches in ISO/FDA-regulated GMP settings. Fluency in English is required.

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