Principal Quality Engineer - Medical Devices & Validation

Kimberly-Clark Corporation is seeking a Principal Quality Engineer in Nogales to ensure the quality and compliance of medical products across manufacturing processes. The role requires coordination of validation protocols and compliance with FDA, GMP, ISO 13485, and 21CFR Part820.

The ideal candidate will possess an engineering background with at least 6 years of quality experience in the manufacturing sector, solid knowledge of process and product quality, and advanced English communication skills.