Número de empleados
Sitio Web corporativo
Aviso de privacidad
Descripción y detalle de las actividades
• Perform various types of audits (quality system, process and product audits) • Perform reviews with suppliers to determine manufacturability of components. • Create supplier performance metrics and report on performance to suppliers and management. • Work as liaison between suppliers and Masimo to ensure highest level of product quality and supplier performance. • Disposition nonconforming materials and initiate follow up activities to ensure proper corrective action and preclude recurrence of rejections. • Work with various engineering disciplines to resolve issues related to supplier quality. • Work with incoming inspection to ensure proper part surveillance. • Ensure alignment of supplier quality metrics with business objectives.
Experiencia y requisitos
send resume: firstname.lastname@example.org English 80% mandatory • Three to five years of experience in supplier management, preferably in the medical device industry (note: Supplier management experience in a highly controlled or regulated industry may be considered); • Auditing experience and training (Certified Quality Auditor and or Lead Auditor Training for ISO Preferably). • Familiarity with Quality Standards (ISO 13485, ISO 9001, FDA QSR, etc.) • Ability to travel (domestic & international) up to 20% of the time; • Strong problem solving ability; • Strong Analytical Skills; • Strong Communication skills in English and Spanish. • Excellent Documentation skills; • Project Management; • Flexibility and adaptability; • Ability to work with minimal guidance from direct supervisor;
Número de vacantes