Quality Manager - Medical Devices & ISO 13485

Celestica is seeking a Quality Manager for Medical Device QMS and cleanroom environments in Spain. The role requires extensive ISO 13485 expertise, regulatory knowledge, and leadership to align global strategies with local operations. You will oversee audits, CAPA processes, and environmental validation across sterile environments. You will manage documentation, supplier testing, and biological monitoring while ensuring strict compliance with FDA/ISO standards. J-18808-Ljbffr