Manufactura e ingeniería

Manufacturing Improvement Engineer Specialist

Baxter · Tijuana, Baja California

Sitio de la empresa: baxter.com

Presencial en Tijuana, Baja California · Tiempo completo

PresencialTiempo completoCierra el 29/11/2026

Descripción

Baxter México – Manufacturing Improvement Engineer Specialist. Responsibilities: Lead and manage Margin Improvement Projects (MIP) in accordance with the plant plan and departmental commitments. / Ensure the timely and effective implementation of assigned projects while preventing any potential impact on manufacturing lines. / Identify opportunities for potential MIP projects through self-initiated ideas related to direct materials used in device manufacturing, including assessing feasibility, project scope, and validating the financial savings associated with the project. / Collaborate with the Procurement department to manage material and/or product quotations as part of the evaluation and feasibility assessment of generated ideas. / Lead and manage Workshops, Kaizen, and/or VAVE events related to idea generation for MIP projects, identifying viable opportunities and providing follow-up with cross-functional teams on generated ideas. / Lead project planning and may direct portions of smaller projects or segments of larger projects, including scheduling, cost monitoring, resource allocation, workforce loading, and related activities. / Develop and complete process validation activities (IQ/SV/OQ/PQ/TMV) according to project plan timelines, along with the required updates to specifications, methods, processes, or procedures that are verified or, when applicable, validated in accordance with Standard Operating Procedures (SOPs) and QSR 820.75 requirements prior to implementation.

Requisitos

Otros requisitos

Bachelor's degree in Mechanical Engineering / Mechatronics Engineering / Electrical Engineering / Electromechanical Engineering / Systems Engineering / or a related field · IndispensableMinimum of five (5) years of experience in a related position · IndispensableExperience 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 · IndispensableExperience writing and executing process validations (IQ/SV/DOE/OQ/PQ) · IndispensableAdvanced English proficiency / both written and verbal communication skills · Indispensable
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