Experteer OverviewIn this role you ensure supplier quality across an international, multidisciplinary environment. You will develop and maintain quality procedures, support KPI analysis, and drive supplier audits and improvements. You partner with R&D, Process Validation, Purchasing, and Regulatory teams to secure robust supplier performance and compliant documentation. This, in turn, helps Enovis deliver clinically differentiated solutions and improved patient outcomes.Retribuzione / BenefitsCreate and maintain Quality Management System procedures and work instructionsManage and collect quality records per QMS proceduresAnalyze supplier quality KPIs and nonconformities trends; perform root cause investigationsQualify and oversee suppliers, including conducting audits as auditorSupport supplier improvement plans after audits and nonconformitiesEvaluate supplier process validation strategies with cross-functional teamsCommunicate with suppliers on product and process quality topicsCollaborate with R&D to modify technical documentation as neededCoordinate with Purchasing to identify new sourcesAssist Post Marketing Surveillance and Incoming Inspection regarding outsourced production issuesSupport Regulatory with supplier process information for registrationsAssist internal inspections by Certification/Notified Bodies and AuthoritiesRecommend corrective actions to minimize nonconformitiesManage initial sampling with suppliersResponsabilitàBachelor's or Master's degree in Engineering (Mechanical, Management, Biomedical, or Bioengineering preferred)Experience in supplier quality assurance in modern manufacturing environmentsStrong Excel and Microsoft Office skillsPrecise and methodical work approach, able to handle multiple tasksTeam player with good communication in English (min B2); basic German is a plusWillingness to travel short-term within Italy and abroadLead Auditor qualification (AICQ-CEPAS, AICQ-SICEV) considered a plus
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