Staff Source Quality Engineer

Johnson & Johnson (Shanghai, 中国) 1天前发布
Full-time
Job summary As a Staff Source Quality Engineer you will be responsible for external suppliers of direct and indirect materials, finished goods and services for our Ethicon franchise. You will lead the deployment of the Source Quality Management (SQM) strategies and associated standards, policies, procedures, programs, systems, processes, and initiatives for suppliers of the Ethicon supply chain. You will actively use the talents and lead teams (SQEs and others), collaborate with Strategic Sourcing/Procurement, R&D, Engineering/Technical Operations, Quality, Operations, business partners/collaborators, and external suppliers to implement solutions and improve suppliers’ quality and overall service and performance. In this role, you will support the development and execution of plans/strategies, and implementation of systems, processes, and procedures to attain and sustain robust supplier/purchasing controls with regards to the determination, selection, qualification, monitoring, and disengagement of suppliers. You will proactively identify, develop, and lead the investigation and resolution of supplier-related challenges, and implements appropriate Quality Engineering methodologies, statistical techniques, process capability analyses/improvements, DOE/process optimization, and other technical or Process Excellence (PEx) tools in support of supplier-related changes, risk management, product/process transfers, innovations, and continuous process enhancements to improve supplier reliability, minimize risks, and ensure balanced sources of material supply capable of meeting or exceeding Quality, Compliance, and Business requirements. Duties & responsibilities Provide timely business support for the assigned Ethicon Supplier Quality Management (SQM) function globally Lead, develop, and implement supplier/purchasing controls and associated activities including Approved Supplier List management. Participate in and/or lead the identification, selection, qualification, monitoring, and disengagement of suppliers for Supplier Quality Management. Collaborate with suppliers and business partners to ensure robust materials, products, processes, and systems. Partner with Procurement, R&D, Engineering/Technical Operations, Quality, Operations, and Suppliers in the timely investigation, resolution/prevention of supplier-related issues to minimize/prevent business disruptions. Monitor and analyze supplier performance metrics, identify areas of opportunity, communicate supplier risks, and drive the resolution of supplier quality issues and risk control processes. Implement supplier change request process including change notification, dissemination of information, impact assessment, approval of changes, and supports material/supplier qualifications. Own, drive, and lead the assigned Supplier Quality related projects, activities, initiatives with limited supervision. Apply Project Management methodologies to plan, organize, connect, shape, lead, and deliver results for SQM projects. Use analytical and problem-solving skills to develop and optimize supplier performance working in conjunction with the Worldwide Supplier Quality Management Team. Analyze quality data and identify trends impacting risk benefits requirements of product and quality systems for external suppliers. Lead discussions to drive resolution. Collaborate with operations and franchise operations development on process/product improvement projects. Prepare Supplier Quality Agreements and drives discussion with supplier while collaborating Supplier Quality Manager. Develop/implement Quality Risk Management process for supplier-related matters with partnerships of subject-matter experts Own and lead the Supplier Quality Relationship Management (SQRM) process for the assigned suppliers (e.g. Lead periodic SQRM meetings including supplier quality performance reviews, supplier investigation follow-ups, investigation responsiveness/cycle time, targeted improvement plans (TIP), closed loop corrective actions, NC reductions, supplier quality metrics, etc.). Understand or anticipate the customer’s needs and makes valuable contributions by providing specific metric information tailored to the particular business environment. Take actions to identify internal customer requirements and translate customer requirements into potential proactive improvements to components or supplier quality systems. Proactively pursue clarification to confirm understanding of internal customer needs and requirements. Follow up on commitments and keeps customer, management and appropriate parties apprised. Respond proactively to changing regulatory and business needs. Lead component qualification change projects in collaboration with key business partners and the supplier’s applicable functional groups. Apply appropriate Quality Engineering and PEx tools (e.g. PM/VSM, Kaizen, DMAIC, FMEA/FTA, RCA, MSA, SPC, Cp/Cpk/Cpm/Ppk, Hypothesis Testing, ANOVA/DOE/EVOP, etc.) to support innovations and continuous improvements Comply with all applicable quality management system, environmental, safety and occupational health policies. (for example, ISO 13485, ISO14001 & OSHAS18001). Qualifications Experience and education A minimum of a Bachelor's degree in Engineering, an Applied Science or a related technical and quality field is required. A minimum of 6+ years of experience in Science, Engineering, or other analytical roles including data analysis, risk assessment and risk mitigation is required. Prior manufacturing, plant or technical background is required. Working experience in good manufacturing practice regulated environment is preferred (medical device, pharmaceutical, etc.). Demonstrated knowledge of manufacturing principles and practices, and procedures. Direct experience in plant and/or supplier GMP auditing is preferred. Broad experience with quality systems, including but not limited to validation, non-conformance, CAPA systems and investigations, laboratory controls, production and process controls, is required. Experience with documentation and technical writing skills, in a regulated compliance environment, is required. Component Qualification/Process Validation experience is preferred. New product introduction experience is desired. Prior experience with FDA inspections is desirable. Broad knowledge of Quality System Regulations and Supplier Quality Management principles is desired. Demonstrated ability to identify compliance risks and assess business impact, is required. Ability to manage complexity and lead a diverse team is essential. Ability to deal with complex issues using deductive reasoning, critical analysis skills and systematic approaches. REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS. Working knowledge of regulatory compliance requirements (i.e. Quality System Regulations (QSRs), Medical Device Directive (MDD), ISO 9001, ISO 13485, ISO 14971 or other international standards) required. Working knowledge of Quality issue investigation, Non-Conformance Reports (NCRs), Corrective and Preventative Actions (CAPAs) preferred. ASQ Certifications for Certified Quality Engineer (CQE), Quality Manager (CQM), and/or Supplier Quality Professional (CSQP) preferred. Quality Auditor qualifications or Lead Auditor certifications such as ASQ Certified Quality Auditor (CQA) or Biomedical Auditor (CBA) preferred. Flawless Project Execution (FPX) or Project Management Professional (PMP) trained and certified preferred. Six Sigma Black Belt/ Green Belt (CSSBB)/CSSGB) or Lean certification from a recognized program or PE leadership training preferred Strong analytical skills, metrics development and ability to identify trends are desirable. Knowledge of specific business practices and software applications skills (Word®, Excel®, PowerPoint®, Minitab®, Visio®, Microsoft Project®) is preferred. Must have strong business acumen. The ability to collaborate with all levels of management in cross-functional team environment is required. Ability to communicate effectively in English. Bilingual in English and other language (Spanish, German, Portuguese, or Mandarin) is preferred. ADDITIONAL POSITION REQUIREMENTS: No additional requirements. Responsibility for others & internal interactions This position reports to Source Quality Supervisor or Senior Source Quality Manager. This position works closely with Procurement/Strategic Sourcing, Research and Development / Design Quality,Product Management, Engineering/Technical Operations, plant associates and Quality Compliance. Physical working conditions / requirements Availability to work extended hours/nights/weekends/holidays may be required. Work to be performed mostly in an office setting with occasional walking and lightweight lifting. Location & travel requirements This position may require up to 35% domestic and international travel. The primary location of the position to be based at ETHICON Somerville, NJ and/or ETHICON office sites. EXTERNAL INTERACTIONS The external interactions may include but are not limited to suppliers and regulatory bodies. Primary Location China-Shanghai-Shanghai- Organization Johnson & Johnson Medical China (7052) Job Function Engineering Requisition ID 2206040337W

More from Johnson & Johnson
Staff Engineer, Ext Mfg Supplier Quality
Johnson & Johnson 1天前发布
Sr. Sourcing Manager - API
Johnson & Johnson 1天前发布
Principal system engineer
Johnson & Johnson 1天前发布

Staff Source Quality Engineer

Apply On Company Site
Back to search page