Celestica Monterrey is seeking a Quality QMS Manager to lead the integral QMS training strategy, oversee CAPA, and ensure ISO 13485 compliance across sites.
The role requires 7–10 years in medical device quality, experience with FDA inspections, and strong leadership to guide cross-functional teams; travel >50% is expected, passport required.
You will harmonize policies, manage controlled documents, and prepare for inspections with a focus on risk management and data integrity.
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📌 Global QMS Manager for Medical Devices (Hybrid) (Ejido de la Finca)
🏢 Celestica
📍 Ejido de la Finca
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