POur mission is to strive to create high-tech implantable devices and diagnostic solutions for cardiac diseases, which are accessible to the greatest number of people, while offering valuable services to patients, physicians, hospitals and health care insurers. /ppThe strongSenior Supplier Quality Engineer (SQE) /strongrepresents MicroPort in managing the quality relationship with the suppliers, throughout the supplier lifecycle from supplier qualification to the manufacturing and to post market life cycle, by considering the customer specific requirements and offering technical support to ensure the fulfilment of the company objectives in compliance with established standards and regulations (e.g.: FDA 21 CFR Part 820, ISO13485, European Medical Device Directives 90/385/EEC and 93/42/EEC, European MDR 2017/745, Japan PAL and ordinance #169, China regulation, Canada MDR SOR/98-282, TGA and any other applicable regulation). /ppTravel availability: approx. 50% /ppstrongYour missions will be as follows /strong: /ppThe purpose of the Supplier Quality Engineer role shall be achieved by: /pulliEnsure Company compliance with the Supplier Management procedure /liliEnsure that suppliers provide services respecting applicable regulations and specifications /liliIdentify and help implement improvement to supplier quality management tools and processes /liliWork with the supplier on their understanding of MicroPort CRM products, their intended use, and regulatory requirements /liliSupporting MicroPort CRM improvement initiatives related to suppliers (i.e. Purchasing group in Cost Reduction projects) /liliPre-production activities /liliContributing to the selection of suppliers with RD, Operation and Purchasing department and qualification through audit process /liliCollaborating with RD in the development and communication to suppliers of component specification documentation, review and approve components specifications, ensuring that specifications cite critical characteristics and required process controls, when required. /liliTechnically develop the supplier throughout the product development process to assure launch readiness, including development of supplier technical capabilities control plans. /liliEstablish quality requirements for suppliers and initiate and manage quality agreements, when required. /liliEnsure that proper risk control measures are implemented and monitored at the supplier. /liliAssist in developing incoming inspection plans for components, assemblies and/or finished devices. /liliUse appropriate methods such as statistical process control (SPC), advanced quality process (AQP) tools and metrics proactively to identify and implement improvement opportunities. /liliPost-production activities /liliInitiate and manage Supplier Corrective Actions (SAR) to ensure complete, timely and effective root cause analysis and corrective action implementation is performed promptly with the appropriate stakeholders. /liliApplying risk management tools and concepts in the decision-making process for any identified opportunities, as well as for the prevention of non-conformances to occur at supplier level. /liliGather, monitor and analyze supplier quality data to identify trends and implement corrective action (Scorecards, KPIs, etc.) and prepare the data for the Quality Management Review. /liliManage Supplier Change Notices and provide leadership in managing the supplier change control process. /liliParticipate in the supplier quality audit process according to the pre-established calendar and ensure follow-up of corrective actions to audit findings /li /ulpThis list of functions is not exhaustive, and other tasks inherent to the position may be performed at the request of the line manager and/or in case of organizational change. /ppstrongYour profile: /strong /ppstrongTechnical skills /strong /pulliKnowledge of requirements EU MDR, FDA, GMP, ISO 13485 /liliKnowledge of use of Quality tools/methodologies (CAPA, Data Analysis, Statistical Techniques) /liliKnowledge of process analysis and continuous improvement tools (Lean, Six-Sigma, Poka-Yoke / Error Proofing, Measurement System Analysis, and Process Failure Mode and Effects Analysis (PFMEA)) /liliKnowledge of Industrial processes /liliAdvanced computer skills (Minitab knowledges appreciated) /liliAbility to negotiate "win-win" situations with internal customers and external suppliers /liliAbility to work in a highly matrixed, geographically and culturally diverse business environment /liliAbility to participate in cross-functional teams and work with others /liliResults Oriented High degree of responsibility and accountability /liliLeadership Skills /liliExcellent verbal and written communication Skills /liliAnalytical thinking Prioritization skills /liliQualified Engineer (Industrial or equivalent). /liliPost graduate studies in matters like Industrial Engineering, Quality, Supplier Management, Operations or others related to the role. /liliFluent in English (written and spoken) and Italian /liliMinimum five (5) years of work experience in highly regulated manufacturing environments and similar roles. /li /ul #J-18808-Ljbffr