Job Summary: Takes full ownership in managing overall quality performance of supplier assigned including maintenance of QMS and meeting our Quality Metrics. Works cross-functionally with internal and external customers to ensure the supplier quality continuously meeting Medline quality requirements; Participates in activities to develop supplier quality system, product quality, manufacture process and category quality strategy. Core Job Responsibility: Manages a bucket of suppliers and works as main point of contact window between suppliers and Corporate QA and Shanghai Office QA. Monitors the suppliers’ maintenance of QMS through vigilance audit with primary focus on P&PC and quality control. Supports/Drives the suppliers to build their own master process validation plan and monitor the execution progress; Coordinates and manages non-conformities with all related stakeholders and suppliers. Directs and collaborates with supplier representatives on quality issues (contain but not limit to complaints, rejections, findings…), ensures timely corrective action implementation (CAPA and SCAR) and contributes to supplier quality improvement programs. Works with suppliers on CAPA follow ups as results of QSR and SA (social accountability) audits. Keeps track of suppliers overall capacity and our volume purchased from them. Works with broader Quality Organization to establish and maintain supplier ratings and executes the program to improve ratings of suppliers assigned to him/her when needed. Coordinates the suppliers’ change requests from the initiation to the end, including standardizing the initiation, leading or assisting to review supplier change requests for assessing impact on product quality and QMS, progress communication, etc.; Transition of QA/QC related knowledge from QE to SQE once the supplier is fully approved for mass production. It includes ensuring the related documents transferring from development to mass production, holding pre-production meeting to align inspection attributes with Medline consistently, and training the QCs (both Medline’s and suppliers’) and production personnel, etc. Identifies and implements improvement opportunities to increase the efficiency and effectiveness of the supplier quality engineering and supplier quality management programs. Work with QC/QA to optimize product inspection criteria with LEAN and effective quality inspection purpose. Completes the other tasks assigned by his/her supervisor or the supplier quality manager. Basic Technical Skills: Familiar with MS office software applications like MS Word, Excel and PowerPoint; Good data analysis skills, utilizing data to dig up and solve problem; Familiar with quality tools, such as 5WHY, Fishbone, SOP etc. Lean & Six Sigma project experience is a plus; Familiar with ISO 9001, internal auditor or knowledge of ISO 13485/QSR 820 is a plus. Qualification: Education level: Bachelor degree in engineering field; 3+ years’ experience on supplier quality management with sound improvement knowledge, working in medical device industry is a plus; Good communication skills, both English and Mandarin; Team Spirit, Integrity, self-motivated and ready to work under pressure; Proven learning and adaption capability. Core Competency (MSF): Sense of urgency Strong work ethic Deliver results Focus on the customer Sound judgement Build effective relationships Show more Show less

JOB SUMMARY: Lead and coordinating activities of purchasing activities for pharma products and other related categories. CORE JOB RESPONSIBILITIES: 1.Project Management Collaborate with product manager, engineering, and vendors to develop new products and bring new products to the market or redesign the products to achieve cost competitiveness. Lead project and influence different functions to achieve goals, assure result accomplish and deliver on time. Know the potential quality risk, know how to improve product cost - increase production efficiency, re-engineering, material changing, etc. Approaches tasks and projects in a streamlined manner; applied knowledge of processes, product, and resources to minimize rework and maximize efficiency. Collaborate with product manager, engineering, and vendors to develop new products and bring new products to the market or redesign the products to achieve cost competitiveness. Identify priorities during whirl wind. 2.Vendor Management Maintain effective business relationship with vendors associated with assigned product categories; Understand vendor impact on overall business and product category; Proactively be aware of potential changes with vendors or in related manufacturing industry; Monitors contract compliance. Leads supplier score card process. Keep challenging existing vendor pool, identify high potential vendors, sourcing risk mitigation plan. Monitors contract compliance. Leads supplier score card process. Develop new product out. 3.Team Work provide solutions, or escalation Collaborate with teams effectively and respectfully; Acts as team player and facilitator among teams. Qualification: 1.Education level: Bachelor’s Degree and above 2.Working experience: Have working experience in procurement function in textile products is a must, the experiences in a health care company or a regional sourcing center will be a plus; Have new product development experience; Have new supplier development experience; 3.Language: English Show more Show less

Job Summary: Takes full ownership in managing overall quality performance of supplier assigned including maintenance of QMS and meeting our Quality Metrics. Works cross-functionally with internal and external customers to ensure the supplier quality continuously meeting Medline quality requirements; Participates in activities to develop supplier quality system, product quality, manufacture process and category quality strategy. Core Job Responsibility: Manages a bucket of suppliers and works as main point of contact window between suppliers and Corporate QA and Shanghai Office QA. Monitors the suppliers’ maintenance of QMS through vigilance audit with primary focus on P&PC and quality control. Supports/Drives the suppliers to build their own master process validation plan and monitor the execution progress; Coordinates and manages non-conformities with all related stakeholders and suppliers. Directs and collaborates with supplier representatives on quality issues (contain but not limit to complaints, rejections, findings…), ensures timely corrective action implementation (CAPA and SCAR) and contributes to supplier quality improvement programs. Works with suppliers on CAPA follow ups as results of QSR and SA (social accountability) audits. Keeps track of suppliers overall capacity and our volume purchased from them. Works with broader Quality Organization to establish and maintain supplier ratings and executes the program to improve ratings of suppliers assigned to him/her when needed. Coordinates the suppliers’ change requests from the initiation to the end, including standardizing the initiation, leading or assisting to review supplier change requests for assessing impact on product quality and QMS, progress communication, etc.; Transition of QA/QC related knowledge from QE to SQE once the supplier is fully approved for mass production. It includes ensuring the related documents transferring from development to mass production, holding pre-production meeting to align inspection attributes with Medline consistently, and training the QCs (both Medline’s and suppliers’) and production personnel, etc. Identifies and implements improvement opportunities to increase the efficiency and effectiveness of the supplier quality engineering and supplier quality management programs. Work with QC/QA to optimize product inspection criteria with LEAN and effective quality inspection purpose. Completes the other tasks assigned by his/her supervisor or the supplier quality manager. Basic Technical Skills: Familiar with MS office software applications like MS Word, Excel and PowerPoint; Good data analysis skills, utilizing data to dig up and solve problem; Familiar with quality tools, such as 5WHY, Fishbone, SOP etc. Lean & Six Sigma project experience is a plus; Familiar with ISO 9001, internal auditor or knowledge of ISO 13485/QSR 820 is a plus. Qualification: Education level: Bachelor degree in engineering field; 3+ years’ experience on supplier quality management with sound improvement knowledge, working in medical device industry is a plus; Good communication skills, both English and Mandarin; Team Spirit, Integrity, self-motivated and ready to work under pressure; Proven learning and adaption capability. Core Competency (MSF): Sense of urgency Strong work ethic Deliver results Focus on the customer Sound judgement Build effective relationships

JOB SUMMARY: Lead and coordinating activities of purchasing activities for pharma products and other related categories. CORE JOB RESPONSIBILITIES: 1.Project Management Collaborate with product manager, engineering, and vendors to develop new products and bring new products to the market or redesign the products to achieve cost competitiveness. Lead project and influence different functions to achieve goals, assure result accomplish and deliver on time. Know the potential quality risk, know how to improve product cost - increase production efficiency, re-engineering, material changing, etc. Approaches tasks and projects in a streamlined manner; applied knowledge of processes, product, and resources to minimize rework and maximize efficiency. Collaborate with product manager, engineering, and vendors to develop new products and bring new products to the market or redesign the products to achieve cost competitiveness. Identify priorities during whirl wind. 2.Vendor Management Maintain effective business relationship with vendors associated with assigned product categories; Understand vendor impact on overall business and product category; Proactively be aware of potential changes with vendors or in related manufacturing industry; Monitors contract compliance. Leads supplier score card process. Keep challenging existing vendor pool, identify high potential vendors, sourcing risk mitigation plan. Monitors contract compliance. Leads supplier score card process. Develop new product out. 3.Team Work provide solutions, or escalation Collaborate with teams effectively and respectfully; Acts as team player and facilitator among teams. Qualification: 1.Education level: Bachelor’s Degree and above 2.Working experience: Have working experience in procurement function in textile products is a must, the experiences in a health care company or a regional sourcing center will be a plus; Have new product development experience; Have new supplier development experience; 3.Language: English

RESPONSIBILITIES Ensure suppliers are clear on all Company and International standards, processes and procedures as they relate to various medical devices. Perform in line and finished product verification in accordance with Company and International Standard to ensure acceptable -quality. Work with other functional team (QA and PM) to determine appropriate testing parameters for the products to ensure limited failures in product. Perform process audits and identify opportunities for continuous improvement on process control, production control and quality control. Be responsible for projects with vendors from a quality perspective, more specifically, on product design change, quality performance improvement, and monitoring quality performance on critical products. Work with Suppliers and Company corporate office in US to help resolve various customer complaints. Specifically, help with root cause investigations and analysis. Implement CAPAs based on root cause investigations to reduce complaint numbers. Ensure that solutions to quality issues are properly implemented and upheld. Work with suppliers and Company QC team in China to reduce product rejections. Work with suppliers to identify opportunities for product and process improvements that lead to cost savings. Work with supplier to validate and optimize the production parameters and ensure suppliers properly document and verify these parameters once implemented. QUALIFICATIONS B.S. Degree in Mechanical Engineering, or Material, or Industrial engineer or Medical device related engineering field required. 3+ years of engineer experience, project management is preferred Understanding of quality system requirements (ISO 13485 or ISO 9001) Ability to read and interpret product specifications and drawings Detail oriented with strong written and verbal communication, problem solving, and organizational skills Professional attitude with a heightened sense of urgency to complete tasks accurately and efficiently. Ability to effectively recognize and suggest improvements for finished products, processes and documentation practices to suppliers, managers, and coworkers. Proficiency of PC skills: AutoCAD or SolidWorks, MS Word, MS Excel, Adobe and E-mail Available to travel frequently. Excellent English speaking, reading and writing skills. Capable of handling special projects as directed by Managers.