.Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Convatec's revenues in 2023 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more about Convatec, please visit Convatec Group.Responsibilities:Development of the supplier quality system.Participate in the supplier audits for new and existing suppliers as per schedule and the appropriate level of documentation as per procedure.Handle the non-conformities/SCARs and Corrective/Preventive actions when escalated, in a timely manner.Participate in Supplier Quality Reviews in collaboration with Category Managers.Active participation on Material Review Boards (MRB).Participate in the approval of new suppliers as per procedure.Assure the supplier evaluations are performed and take actions accordingly. Responsible for immediate communication and the follow-up on the final disposition of raw material (non-conformance, acceptable materials, etc.) in adequate time and according to approved procedures.Participate in root cause analysis, NC reviews, analysis of FMECA's, coordinate investigations, etc. if required.Manage QA/QC related activities in relation to new and existing tools approval processes.Drive continuous improvements in relation to total cost ownership, speed, optimization etc. by use of known LEAN techniques in collaboration with supplier and stakeholders.Actively participate in various new product development, product transfer and other optimization projects.Promote teamwork among his area and other areas.To comply with the company quality policy.Follow up, development, and compliance according to the Quality Management System based on the regulations and standards of ISO 13485, FDA, GMP, MDR.Requirements:Bachelor's degree (Industrial area or similar), required.Three years as Supplier Quality areas experience, preferred.Measurement equipment knowledge skill preferred.Written and spoken English required.Internal Auditor required.Experience of quality tools, statistic techniques (SPC, etc.) preferred.Software utilization skills / Computer skills required.Ability to coordinate multiple projects, project planning and work cohesively with all involved departments.General knowledge of injection molding processes preferred.Familiar/knowledge on ISO 2859-1 (AQL values and sampling plan).Familiar/knowledge on basic requirements of FDA QSR's GMP's and ISO 13485, MDR or similar regulations, required