Manufactura e ingeniería

Senior Manufacturing Engineer

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 – Senior Manufacturing Engineer. Responsibilities: Lead the transfer and integration of manufacturing processes from other Baxter facilities, ensuring successful implementation, validation, and operational readiness. / Drive continuous improvement initiatives that increase productivity, improve first-pass yield, reduce scrap, and enhance overall manufacturing performance. / Design, develop, and implement manufacturing tools, fixtures, inspection equipment, and process improvements that support safe and efficient production. / Analyze manufacturing data, identify performance trends, investigate root causes, and implement corrective actions to improve quality and operational results. / Plan and support manufacturing capacity strategies, including equipment, labor, space utilization, and maintenance considerations to meet business demands. / Lead or contribute to process validation activities, including IQ, OQ, PQ, and related verification efforts, ensuring compliance with quality and regulatory requirements. / Collaborate with suppliers, operations, quality, and cross-functional teams to solve complex technical challenges and successfully execute engineering projects.

Requisitos

Otros requisitos

Bachelor's degree in Mechanical Engineering / Manufacturing Engineering / Industrial Engineering / or a related engineering discipline · Indispensable3-5+ years of experience in manufacturing engineering / process development / process transfer / or continuous improvement within a regulated manufacturing environment · IndispensableExperience leading validation of end-to-end manufacturing processes · IndispensableExperience with IQ/OQ/PQ methodologies is highly desired · IndispensableDemonstrated ability to identify manufacturing issues / perform root cause analysis / and implement sustainable corrective actions · IndispensableExperience working cross-functionally with operations / quality / suppliers / and technical stakeholders to deliver business results · IndispensableStrong project management / organization / and prioritization skills with the ability to manage multiple initiatives simultaneously · IndispensableEffective communication skills with the ability to provide technical guidance / influence stakeholders / and lead project activities · IndispensableExperience within the medical device / healthcare / life sciences / or other highly regulated manufacturing industries · IndispensableKnowledge of FDA Quality System Regulations (21 CFR Part 820) / ISO 13485 / CAPA processes / and quality system requirements · Indispensable
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