Manufacturing Improvement Engineer (Lean & GMP)

Baxter International Inc.; Tijuana; Presencial; MXN 1.508.000 - 2.040.000; Jornada completa

Descripción de la vacante

Baxter International Inc. is seeking a seasoned engineer to drive the integration and improvement of mechanical device manufacturing processes. You will own significant projects, driving cost, timeline, and quality objectives while advancing validated production methods.

Ideal candidates have 5+ years in related roles, experience in ISO/FDA environments, and strong Lean/Six Sigma credentials, with advanced English proficiency.

Formación

• Bachelor's degree in Mechanical, Mechatronics, Electrical, Electromechanical, Systems Engineering or related field.
• Minimum of five (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 in ISO/FDA-regulated environments and GMP requirements.
• Experience writing and executing process validations (IQ/SV/DOE/OQ/PQ).
• Advanced English proficiency in writing and speaking.

Responsabilidades

• Lead and manage Margin Improvement Projects (MIP) per the plant plan.
• Ensure timely and effective implementation of projects without impacting lines.
• Identify opportunities for MIP ideas, assess feasibility and financial savings.
• Collaborate with Procurement for material/quotations during evaluation.
• Lead Workshops, Kaizen, and VAVE events for MIP ideas and follow-up with cross-functional teams.
• Lead project planning and direct portions of smaller or segments of larger projects.
• Develop and complete process validation activities (IQ/SV/OQ/PQ/TMV) per SOPs and QSR 820.75.

Conocimientos

Lean practices

Six Sigma

Project management

Leadership

Problem solving

Production transfers

GMP compliance

ISO FDA environments

Educación

Bachelor's degree in engineering

Descripción del empleo

Baxter International Inc. is seeking a seasoned engineer to drive the integration and improvement of mechanical device manufacturing processes. You will own significant projects, driving cost, timeline, and quality objectives while advancing validated production methods.

Ideal candidates have 5+ years in related roles, experience in ISO/FDA environments, and strong Lean/Six Sigma credentials, with advanced English proficiency.