Manufacturing Improvement Engineer - Lean & GMP

Baxter Healthcare

Tijuana

Híbrido

MXN 350.000 - 550.000

Jornada completa

hace 45 horas
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Descripción de la vacante

Baxter Healthcare in Mexico seeks a Mechanical Engineer to drive process improvements and manufacturing excellence. You will manage Margin Improvement Projects, ensuring on-time delivery and cost savings while maintaining GMP-compliant processes.

Responsibilities include leading workshops, coordinating cross-functional teams, and validating processes per IQ/SV/OQ/PQ/TMV standards. Strong problem-solving, leadership, and advanced English are required.

Formación

  • Bachelor's degree in Mechanical Engineering or related field.
  • Minimum of five (5) years of experience in a related position.
  • Experience in ISO/FDA-regulated environments and GMP requirements.
  • Experience writing and executing process validations (IQ/SV/DOE/OQ/PQ).
  • Advanced English proficiency, both written and verbal.

Responsabilidades

  • Lead and manage Margin Improvement Projects (MIP) per plant plan and dept commitments.
  • Ensure timely and effective project implementation with no impact on manufacturing lines.
  • Identify opportunities for MIP via direct materials cost savings and project scope validation.
  • Collaborate with Procurement to manage quotations in evaluation/feasibility of ideas.
  • Lead Workshops, Kaizen, and VAVE events for MIP, with cross-functional follow-up.
  • Lead project planning and direct portions of smaller or segments of larger projects, including scheduling and cost monitoring.
  • Develop and complete process validation activities (IQ/SV/OQ/PQ/TMV) per plan and SOPs.

Conocimientos

Project management
Lean practices
Six Sigma
Problem solving
Leadership

Educación

Bachelor's degree in Mechanical Engineering

Descripción del empleo

Baxter Healthcare in Mexico seeks a Mechanical Engineer to drive process improvements and manufacturing excellence. You will manage Margin Improvement Projects, ensuring on-time delivery and cost savings while maintaining GMP-compliant processes.

Responsibilities include leading workshops, coordinating cross-functional teams, and validating processes per IQ/SV/OQ/PQ/TMV standards. Strong problem-solving, leadership, and advanced English are required.

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