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 general strategies with local operations.
Es posible que un gran número de candidatos se presenten a este puesto, así que asegúrese de enviar su CV y su solicitud lo antes posible.
You will oversee audits, CAPA processes, and environmental validation across sterile environments. xhfqzwm You will manage documentation, supplier testing, and biological monitoring while ensuring strict compliance with FDA/ISO standards.