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電子商務有限公司技術部管理制度(編輯修改稿)

2025-06-19 04:59 本頁面
 

【文章內容簡介】 nformation Technology, Engineering, Professional Services Within the following industries: Electronics, Automotive Motor Vehicles Parts, Computer Hardware Our privacy policy: Your resume and information will be kept pletely confidential. Looking forward to receiving your resume through our website and going over the job in more detail with you! CyberCoders, Inc is proud to be an Equal Opportunity Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, disability, sexual orientation, ancestry, marital or veteran status. 【 技術部規(guī)章制度 】 第 8 頁 共 29 頁 項目經(jīng)理 Project Manager 職責(適用于中國) 計劃: a)項目范圍、項目質量、項目時間、項目成本的確認。 b)項目過程 /活動的標準化、規(guī)范化。 c)根 據(jù)項目范圍、質量、時間與成本的綜合因素的考慮,進行項目的總體規(guī)劃與階段計劃。 d)各項計劃得到上級領導、客戶方及項目組成員認可。 組織: a)組織項目所需的各項資源。 b)設置項目組中的各種角色,并分配好各角色的責任與權限。 c)定制項目組內外的溝通計劃。(必要時可按配置管理要求寫項目策劃目錄中的《項目溝通計劃》) d)安排組內需求分析師、客戶聯(lián)系人等角色與客戶的溝通與交流。 e)處理項目組與其它項目干系人之間的關系。 f)處理項目組內各角色之間的關系、處理項目組內各成員之間的關系。 g)安排客戶培訓 工作。 領導: a)保證項目組目標明確且理解一致。 b)創(chuàng)建項目組的開發(fā)環(huán)境及氛圍,在項目范圍內保證項目組成員不受項目其它方面的影響。 c)提升項目組士氣,加強項目組凝聚力。 d)合理安排項目組各成員的工作,使各成員工作都能達到一定的飽滿度。 e)制定項目組需要的招聘或培訓人員的計劃。 f)定期組織項目組成員進行相關技術培訓以及與項目相關的行業(yè)培訓等。 g)及時發(fā)現(xiàn)項目組中出現(xiàn)的問題。 h)及時處理項目組中出現(xiàn)的問題。 控制 a)保證項目在預算成本范圍內按規(guī)定的質量和進度達到項目目標。 b)在項 目生命周期的各個階段,跟蹤、檢查項目組成員的工作質量; c)定期向領導匯報項目工作進度以及項目開發(fā)過程中的難題。 d)對項目進行配置管理與規(guī)劃。 e)控制項目組各成員的工作進度,即時了解項目組成員的工作情況,并能快速的解決項目組成員所碰到的難題。 f)不定期組織項目組成員進行項目以外的短期活動,以培養(yǎng)團隊精神。 結語: 項目經(jīng)理是在整個項目開發(fā)過程中項目組內對所有非技術性重要事情做出最終決定的人。 職責(適用于國外) ? Drives PMO sponsored PDP initiatives and projects to establish metrics, continuously improve cycle time, efficiencies, and pliance in medical device product development such as but not limited to: 【 技術部規(guī)章制度 】 第 9 頁 共 29 頁 ? Training Core Team leaders and core teams on the PDP, and in Standardizing project management tools, techniques and best practices ? Leaning out the design control process and documentation ? Supporting the Portfolio planning and roadmap process ? Tracking and analysis of key product development and Ramp。D metrics ? Works with Core team leaders and functional managers to support PMO’s resource allocation and planning process ? Increase the level of pliance and enforce quality practices within core teams (. facilitate Design Reviews, Key Learnings, etc.) ? Assisting core teams with creating work breakdowns, schedule development and critical chain analysis ? Provides project management expertise for a small to medium sized projects. Leads a multifunctional core team from Concept through Commercialization。 establishes project plans and objectives, develops cost analysis, creates and manages the project schedule and budget。 tracks progress and updates key stakeholders on project status. Resolves resource allocation issues, conflicts, and priorities to ensure projects are staffed appropriately, pleted on time, and within budget constraints. Ensures efficient transfer of product from Ramp。D to manufacturing and external marketing. ? Facilitates and drives the core team to successful pletion of design control processes such as design and development planning, FMEAs, requirements development and management, design reviews, verification, validation, and post market monitoring. ? As necessary, performs other duties as required. Qualifications: Education: ? Requires a bachelor’s degree in Engineering or equivalent training 【 技術部規(guī)章制度 】 第 10 頁 共 29 頁 ? Master’s degree is a plus Knowledge and Experience: ? 5+ years experience in the medical device industry, intravascular medical devices preferred ? Requires 25 years project management experience in an FDAregulated and/or ISO 14971 certified industry, managing 2030 team members ? Knowledge and experience with various software lifecycles, such as Waterfall, Agile environment a plus ? Experience in a multiplatform (Windows/LINUX) and/or distributed puting environment。 ? Experience in a geographically distributed environment ? Knowledge and experience with CaliberRM, Siemens PLM ? Knowledge of 21CFR Part 820 on Design Controls and experience in the practical application of these regulations on engineering processes and documentation ? Knowledge and understanding of ISO standards on Medical Devices and Risk Management ? Experience with the application of six sigma tools on design processes and/or projects ? Experience with application Design of Experiments (DOE) on design optimization, verification, and validation ? Experience in managing projects from inception to postmarket sustaining using a phasegate methodology ? Strong understanding of engineering principles, theories and Additional Desirable Qualifications: ? Certificate in Project Management, preferred ? Six Sigma Green Belt certification preferred, Black Belt certification a plus 【 技術部規(guī)章制度 】 第 11 頁 共 29 頁 Skills and Abilities: ? Proficient in the use of Project Management Tools for planning, scheduling, task estimation ? Advanced Microsoft Office skills in the following applications: o MSProject: Resource loading, tracking o Excel: Forms, Formulas, Functions, Pivot Tables, amp。 Graphs o PowerPoint: Graphics amp。 Animation o ECO writing/review using Agile software ? Ability to municate effectively both orally and in writing and to establish and maintain cooperative working relationships with persons contacted in the course of performing assigned duties including Company management and outside business associates ? Ability to interact with senior management on a regular basis ? Ability to represent the Company at professional and business functions in a petent manner ? Excellen
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