Funciones del Puesto
Responsible for the facilitation of all supplier, and regulatory audits for all locations, oversee SCAR administration, standards coordination leadership, quality and regulatory training, and provide support for the Quality Management Review.
Requisitos del Puesto
BS in Industrial Engineering or related field. It could be sciences or Technical Discipline
Knowledge on ISO 14971 & 13485 AND Knowledge on CRF 820 CGMPs is a plus
Experience in a Medical Device Company
Experience in Supplier Management
Travel is required.
Work in an office environment with varying amounts of walking, sitting, standing, twisting, turning.