Supplier Capability and Process Engineer

Antal platser:
Yrkesbenämning: Civilingenjör, tillverkningsindustri
Publicerad: 2019-06-10
Sista ansökningsdag: 2019-07-28
Role Summary:We are a $5 billion business with more than 11,000 individuals in over 100 countries. GE Healthcare Life Sciences works with cutting edge technology enabling and advancing the discovery, diagnosis and medical treatments of the present and the future. Join the GE Healthcare Life Sciences as Supplier Capability and Process Engineer.Essential Responsibilities:In this role you will be responsible for driving exceptional product quality for our customers and optimized Cost of Quality for GEHC. This is a key technical position, affecting product quality for both installed base and new product introductions, by driving supplier capability assessment and development along with a robust hand-off between GEHC engineering and our suppliers.Effectively assess and evaluate supplier capabilities used in the supplier selection processImprove supplier quality performance for assigned suppliers/parts via Quality Plan ImplementationDevelop positive relationships and work closely with Sourcing Leaders to manage and implement supplier/engineering changes, New Product Introductions, and Supplier TransfersInterface with Suppliers, Engineering, Service, Manufacturing and Sourcing to drive quality improvements that minimize the Costs of QualityAssure Corrective and Preventive Action plans are developed and executed at assigned suppliers in compliance with the CAPA processResponsible for leading root cause investigations and corrective actions to resolve supplier quality related issuesSupplier part and process qualification activitiesEstablish and maintain positive relationships with external and internal interfaces to ensure that customer requirements are understood and achieved – suppliers, engineering, service, manufacturing, sourcing, supplier qualityQualifications/Requirements:Bachelor’s Degree in Engineering - Mechanical, Production, Industrial or equivalent knowledge/experienceSignificant experience from Life Sciences, Pharma or Medical device industrySignificant experience in manufacturing, design, quality assurance or regulatory assuranceExperience in problem solving, root cause analyses and leading and influencing others to drive change (cross functionally and globally)Experience with Quality Management System tools, continuous improvement methodologies and in-depth understanding of site level products and related processesDemonstrated ability to lead, acknowledge, develop, communicate & implement a strategy to ensure complianceValid EU work permitDesired Characteristics:A Bachelor's Degree in Engineering (or equivalent knowledge/experience)Significant commercial sourcing experience in all facets of the assigned commodities  Excellent negotiations skills and analytical skills with the ability to manage and develop supplier relationships Ability to energize, develop and build rapport at all levels within an organization Proven ability to execute and deliver on commitments Experience implementing a compliant supply chain Greenbelt certification preferred

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