5 years in medical device supplier quality experience.Experience in root cause identification and problem solving.Experience in quality system audits.Experience in supplier corrective action requests.Experience in technical discussions.Experience in quality review board and change control review board meetings.Experience in process optimization and/or improvement.Experience in mitigating risk by working with the suppliers to document process flow charts, pfmeas, control plans, and iq/oq/pq documentation.Experience in fda regulations, other regulatory requirements, company policies, operating procedures, processes, and task assignments.Experience in maintaining positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and suppliers/vendors.Experience in contributing to the development, maintenance, and improvement of butterfly network’s supplier quality program, system, and procedures.Experience in working in a timeline driven environment.Experience in working in a geographically diverse business environment.Experience in operating in an electronic quality management system.Experience in leveraging and/or engaging others to accomplish projects.Experience in working independently and managing the electronic supplier quality management system in trackwise digital qms.Experience in working knowledge of current regulations and guidelines such as: GMP, ISO 13485; ISO 14971, FDA 21 CFR Part 820; (EU) 2017/745 (MDR).