QUALITY ENGINEER

Business Improvements Support quality improvement initiatives such as process and product characterizations that lead to continuous / cost improvements.
       支持质量改进活动，对产品/制程进行持续改进和成本改善。 Review/analyze the effectiveness of PDCA, Six Sigma, Kaizen, Lean Techniques and/or other improvement tools and programs.
       评估和分析质量工具及项目的有效性，比如PDCA，六西格玛，改善，精益技术和/或其他改进工具。 Conduct benchmarking to develop more effective methods for improving quality.
       通过标杆管理开发更有效的质量管理方法提升质量。 Supports the development of quality engineering and quality compliance with the right skill sets for new product introductions, and product life cycle management.
       开发合适的质量管理方法应用于质量工程和质量合规的发展，运用在新产品导入和产品生命周期管理。 Compliance/Regulatory 合规管理 Review/analyze whether current product and processes (including actions or decisions conducted) are in compliance to standards such as the QSRs, ISO , etc.
       评估和分析现有产品和过程是否合规，比如QSRs，ISO等法规要求 Champions compliance to applicable Global Regulations and standards (e.
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QSRs, ISO, EN and Medical Device Directive (MDD) requirements) including providing support during internal and external audits.
       支持工厂的内外部审核，遵守适用的法规和标准(例如QSRs, ISO, EN和MDD)要求。 Conduct periodic line audits to assess for production controls such as lot segregation.  Review results of area audits to ensure that corrective and preventive actions are adequate.
       执行周期审核评估生产现场是否合规。审阅区域审核的结果确保纠正和预防措施有效。 New Product/Process Introduction 新产品 / 过程导入 Partners with R&D and other cross functional partners to ensure the proper application of design controls, risk management and the investigation/correction of design failures/challenges.
       协调研发和其他的跨部门合作确保相关领域质量管理可控。比如设计管理，风险管理，研发失效的调查/纠正等方面。/ Supports new product introduction as part of design transfer.
       支持新产品导入业务活动，作为研发项目转移的一部分。 Product Quality, Control & Disposition and Performance Standards 产品质量控制处理和执行 Supports activities related to the Material Review Board.
       支持材料审核相关业务活动 Conduct investigation, bounding, documentation, review and approval of non-conformances, CAPAs and customer complaints.  Escalation of quality issues as appropriate.
       执行NC，CAPA和客户投诉的调查分析，审阅和批准。 Accountability and ownership for material identification, material segregation, classification of defect types including the successful application of these techniques on a day-to-day basis in manufacturing.
       监督和处理生产现场日常发生的问题，比如材料标识、物料隔离、缺陷分类等。 Analyze/review effectiveness of preventive and corrective actions.  Review root cause investigation according to an established process.
分析审阅纠正预防措施的有效性。根据确定的过程审核根本原因调查的有效性。 Accountability and ownership of Quality metrics including maintenance and reviewing of leading and lagging indicators of quality 监督和完成公司的质量指标，包括维护和检查质量相关的领先和滞后指标。 Product/Process Validation 产品 / 过程确认 Initiate, review, approve, execute validation or verification documents, such as IQ, OQ, PQ, TMV, Software Validation documents etc., as the engineer/representative/lead/SME of Process Validation/CSV/CSV-E according to the arrangement of work.
根据工作安排，作为过程确认、CSV、CSV-E的工程师、代表、组长或者主题专家，起草、评审、批准和/或执行确认/验证文件，例如安装鉴定、操作鉴定、性能鉴定、测试方法确认、软件确认等文件。 Production/Process Controls including Control Plans 产品 / 制程控制包括控制计划 Partners with J&J Global Supply chain, Finished Goods and material suppliers to ensure appropriate application of process validation, process control, and risk management; and the investigation/correction of process failures when needed.
       协调与沟通强生全球供应链合作伙伴,成品和材料供应商,以确保所有的质量业务活动满足要求，比如过程验证，过程控制，风险管理，过程失效的调查/校正过程。 Conduct stakeholder analysis to ensure that customer CTQs are known and adequately addressed in control plan.
       协调沟通利益相关方，以确保客户的关键质量特性在控制计划里完全体现。 Develop measurement systems/capabilities, destructive tests, non-destructive tests for manufacturing processes.
       开发生产过程中应用的测量系统分析，破坏性测试，非破坏性测试。 Develop control plans consistent with product classification, potential defect types, defect frequency, severity, patient risk, process capability, process controls, etc.
       创建控制计划保证质量系统可控，包括产品标识，潜在缺陷类型，缺陷频次，严重度，病人风险，过程能力，过程控制等。 Develop, interpret and implement appropriate process monitoring and control methods consistent with the level of process/product risk.
       开发、解释和实施适当的过程监视和控制方法与过程/产品风险的水平一致 Collect data and execute/conduct various analytical/statistical analysis and interpretation as part of process improvements and day-to-day support.
       收集数据和执行进行各种分析/统计分析和指导，作为过程改善和日常工作支持的一部分。 Develop, interpret and implement standard and non-standard sampling plans.
       开发、解释和实施标准和非标准的抽样计划。 Assess effectiveness of measurement tools, destructive tests, non-destructive tests, measurement system analysis.
       评估测量系统的有效性。包括测量工具,破坏性测试,非破坏性测试,测量系统分析。 Accountability and ownership for sampling plans of all types including acceptability of risk given the product classification, potential defect types, defect frequency, severity, patient risk, process capability, process controls, etc.
including assessing, applying and interpreting acceptance sampling standard for manufacturing data.
       监督和完成生产制造中各种类型的质量抽样计划，包括可接受性的产品分类、潜在缺陷类型、缺陷频率、严重程度、患者的风险,过程能力,过程控制等。也负责评估、应用和解释相关的生产数据的验收抽样标准。 Assess and interpret common versus special cause variation in manufacturing processing and determine adequacy of current process limits.
       评估和分析生产制造中普通和特殊原因的变异，并确定合适的制程控制临界点。 Risk Mitigation 降低风险 Document, justify, review or analyze whether a proposed change to a process will not enhance the risk level in some way beyond capability of current controls or whether change will result in potential non-compliance to a required standard such as the QSRs.
       记录,证明,检查或分析相关过程变更在某些方面是否增加了风险等级，或者相关过程变更是否会导致潜在的不合规。 Assess the need for risk mitigation techniques given product classification, potential defect types, defect frequency, severity, patient risk, process capability, process controls, etc.
Determine effectiveness of these techniques on previously implemented improvements.
       评估风险消减的技术支持，包括产品分类，潜在缺陷类型，缺陷频率，严重度，患者风险，过程能力，过程控制等。确定之前已经实现改善的技术支持的有效性。 Strategic 战略 Ensures effective quality strategies are created for the validation of test methods, process and design.
       确保建立有效的质量战略，包括测试方法，过程和设计的确认。 Location 地点 This position may require up to 10% travel and will be based in an MD&D manufacturing facility.
        该职位需要10% 的出差，在MD&D生产工厂之间。 Qualifications A minimum of a Bachelor’s Degree, preferably in Engineering or related technical field.
Generally requires 4-6 years related experience.
       学士学位及以上，优先工程和相关技术专业。4-6年相关工作经验 Experience working in both an FDA and European regulatory environment is preferred.
       同时拥有FDA及欧洲法规工作环境的优先 This position will require relevant experience working in manufacturing/operations.
       该职位需要生产/运营相关的工作经验 Experience with a proven track record of implementing appropriate risk mitigation.
       该职位需要相关的实现风险降低方面的可靠的工作经验 Technical training and experience using Statistics, Lean and Six Sigma Methodologies is required including Measurement System Analysis, SPC, DOEs, Reliability, etc.
       该职位需要相关的质量管理技术及经验，使用统计，精益，六西格玛的方法，包括测量系统分析，统计过程控制，实验设计，可靠性等。