sr. supplier quality engineer岗位职责

JOB SUMMARY
Determines appropriate Inspection processes directs IQC personnel, where applicable, in executing day to day activities. Leads containment resolution of supplier quality issues with the manufacturers communicate status on non-conforming parts/suppliers across all programs. Evaluates supplier performance, drives supplier improvements corrective actions through the SCAR process.

ESSENTIAL DUTIES RESPONSIBILITIES
Defines, develops implements Supply base strategies that drive improvements is supplier selection, development, leverage across customer programs fquality improvements cost savings.
Provides regular updates to Quality Engineering Manager on the execution of the strategy.
Provides support fNPI activities by participation in the AQP process as required
Ensures that all production critical supplier issues are resolved in a timely manner, corrective actions are implemented.
Defines develops the appropriate Inspection Plans Inspection Methods, directs Receiving Inspection Auditors
Defines develops the inspection processes via inspection aids instruction guidelines.
Ensuring ongoing site supplier evaluation is performed. This would be achieved by using site information collected from Receiving Inspection, MRB, Customer Returns, SCAR database by liaison efforts with customer work cells. Performance will be reported internally, to the supplier, to the customer where applicable.
Monitors drives PPM issues with the supply base in addition to helping them achieve “Dock to Stock” certified with Jabil (in accordance to the vendperformance system).
Reviews all supplier discrepancies. Coordinates tracks the corrective/preventative action effort.
Proactively communicate information issues that may impact the product costs manufacturability to all affected departments.
Provides insight assistance of implementing maintaining Process Improvement Optimization concentrating on proactive methodologies with the supply base.
Leads SCAR – Supplier Corrective/Preventive Action process fproblem resolution continuous improvement, including critical analysis of supplier DOE, CPK, Gauge R&R studies
Adhere to all safety health rules regulations associated with this position as directed by supervisor.
Comply follow all procedures within the company security policy.
Site RoHS subject Matter Expert
May perform other duties responsibilities as assigned.

MANAGEMENT & SUPERVISORY RESPONSIBILITIES
Typically reports to Management. Direct supervisjob title(s) typically include: Quality Manager
Job is not directly responsible fmanaging other employees (e.g., hiring/termination and/pay decisions, performance management).

JOB QUALIFICATIONS
KNOWLEDGE REQUIREMENTS
Strong electro / mechanical background desired; knowledge of plastic injection molding & tooling, metal stampings & tooling, metal fabrication, machining various electrical components, connectors, PCB & PCBA, cable assembly, full assembly integration etc.
Able to read interpret mechanical drawings (6 sigma training desired).
Good skills in MS excel, word, power point, visio, project.
Understanding of the quality system, medical commercial regulatory requirements how they relate to the business.
Proficiency in use of personal computers, Microsoft Office products (Excel, Word PowerPoint) e-mail skills required.

EDUCATION & EXPERIENCE REQUIREMENTS
Bachelor’s degree required, Bachelor’s degree in Engineering preferred.
3-5 years of experience in Quality Manufacturing Engineering
an equivalent combination of education, training experience.

Key Responsibilities:
• Oversee manage supplier quality performance, conduct supplier audits, ensure supplier compliance with quality standards.
• Collaborate with suppliers to identify rectify quality issues. Use problem-solving techniques, Six Sigma tools, statistical analysis, other methodologies to improve supplier quality.
• Drive continuous improvement initiatives with suppliers to enhance quality, reduce cost, improve supply chain efficiency.
• Supplier Development: Develop maintain partnerships with suppliers. Train suppliers on quality requirements monittheir performance.
• Review supplier manufacturing processes, collaborate with engineering procurement teams to define process parameters, ensure that supplier processes meet quality requirements.
• Ensure proper documentation of supplier quality data, audits, non-conformances, corrective actions, quality tests.
• Ensure suppliers comply with relevant regulations standards in their products processes.
• Manage projects related to supplier quality, such as new supplier qualifications, process changes, corrective action implementation.
• Ensure product integrity by the execution of the product quality architecture strategy (APQP IATF Core tools)
• Perform Quality Systems, Process Product Audits, using applicable Quality Standards specifications– to ensure that processes comply with Corning Quality Requirements.
• Collaborate with the various Corning Supplier Quality teams
• Provide periodic progress updates on execution of the roadmap
Experiences/Education:
Required:
• Bachelof science in engineering
• 5-7 years of experience in quality assurance, quality engineering, a related field
• 2 plus years of experience in supplier quality management supplier development
• Strong knowledge of quality systems standards
• Proficient in quality-related tools methodologies, such as Six Sigma, statistical analysis, etc.
• Excellent problem-solving project management skills
• Strong communication interpersonal skills
Desired:
• Certified DMAIC Black Belt
• Knowledge of ERP/QMS platforms (SAP, ETQ, SharePoint, Windchill)
• Certified Quality Engineer (CQE)
• TL9000/ISO9001 Auditexperience is plus

工作内容：
• 主导供应商质量管理流程的维护。维护合格供应商数据及合格供应商清单，定期更新；
• 制定供应商审计年度计划，组织实施常规的供应商审核，推动供应商的持续改进工作；根据供应商开发需求，组织对新供应商实施供应商审核，参与供应商的认证工作。
• 接收进料检验、内部生产和检验以及后市场关于供应商产品质量的反馈，驱动和监控供应商纠正预防措施，推动持续改进，确保其满足产品要求。
• 配合供应商采购战略，组织开展重点供应商能力提升活动。
候选人要求：
• 本科及以上学历，5年以上医疗器械SQE相关经验。
• 英语可作为工作沟通。
• 良好逻辑性和沟通能力。
• 抗压能力强，可接受出差。