pr失业两个多月了啊，最近形势这么差么

本人原来做半导体设备方面的，专业材料学，现在本行业，跨行业一直在找工作，一点机会都没有啊看来，惨淡。
版上谁有合适的工作，兼职，intern都可以啊，有介绍的么？1。 继续跨行业找，等待。
2。 做老本行。失业一个多月的pr飘过:'(没关系，加油加油，我除了失业比你更惨
你什么行业跨行业，基本面试都没有啊，总不能去做服务员之类的吧，这样跨也没意思
老本行现在也难，经济城狗屎了都没关系，加油加油，我除了失业比你更惨
你什么行业engineer:(什么行业engineer啊electrical engineer
最近是不是经济萧条啊，找了一个多月了一点消息都没有，跨行和不跨行的都试了，pr也没用了吗？还是1月份会好点electrical engineer好点吧，不过最近听我朋友说好几家公司都裁人了，我说半导体方面的啊
你跨行都申请很么行业了？现在身边有很多朋友都失业，要保持乐观的心态。都是裁人还是裸辞的？你多大了年底很多人跳槽， 过了新年会有很多机会而立之年了都那些拿到bonus的赶紧辞职吧，呵呵我没拿到BONUS也辞职了。。貌似就业形势很严峻你这只猫很不乖啊
为什么不先介绍我进去你再辞职？无辜本人原来做半导体设备方面的，专业材料学，现在本行业，跨行业一直在找工作，一点机会都没有啊看来，惨淡。
版上谁有合适的工作，兼职，intern都可以啊，有介绍的么？1。 继续跨行业找，等待。
2。 做老本行。失业一个多月的pr飘过:'(没关系，加油加油，我除了失业比你更惨
你什么行业跨行业，基本面试都没有啊，总不能去做服务员之类的吧，这样跨也没意思
老本行现在也难，经济城狗屎了都没关系，加油加油，我除了失业比你更惨
你什么行业engineer:(什么行业engineer啊electrical engineer
最近是不是经济萧条啊，找了一个多月了一点消息都没有，跨行和不跨行的都试了，pr也没用了吗？还是1月份会好点electrical engineer好点吧，不过最近听我朋友说好几家公司都裁人了，我说半导体方面的啊
你跨行都申请很么行业了？我做的是海上通讯。。 卫星； 导航；雷达； 追踪什么的。我做的半导体设备方面
学的是材料方面，所以设计这两个方面的都去找，未果。。。半导体前景不太好。。几年前就开始下滑了， 很多做这个行业的人都陆续回国了。
制造业今年也不太好，大批裁人呢， 经济不景气， 金融业也首当其冲呀。
祝好运。心想你说不定能给俺介绍一个。。。隔行如隔山。。 除了祝你好运也帮不上什么跨行犹如翻山啊。。。跨行找工作 需要从头做起 要想想看是否值得求被猎！
和你同一个行业还要看有没有机会我公司好像招medical engineer 之类的需要什么背景么？可以内推么？谢谢可以内推，我晚上去公司查查看有什么职位招聘再告诉你虽然不知道背景是不是符合，不过还是多谢你了，真是好人啊呵呵，举手之劳了请问有消息了么？奇怪，我昨天回复你的详细招聘要求怎么没了，再发一次，悲剧Job Openings as at 20 December 2012 ProductLifecycle Engineer Main Responsibilities: Product LifecycleManagement ·        Establishing appropriate master data settingsto facilitate product ramp-up or phase-out strategies·        Collaborate with local and global teams toensure that product lifecycle strategies are implemented properly usingmaterial master data in the SAP system.·        Ensure alignment of Material master andProduct settings in Factory works and Enovia.·        Enhance/ Develop local  procedures tomanage Product Lifecycle and Material master management process. Manufacturing Master Data and Change management·        Work closely with Quality/ Engineering/Supply chain to ensure accuracy of relevant information on Materials/ BOM andRoutings for new products/ materials.·        Determining correct material master data fornew materials, products and Bill of Materials.·        Act as a focal point to drive Master dataalignment across various systems including Factory works, SAP, Indysoft andEnovia.·        Support configuration activities related toproduct or process changes, ECR, ECO, MCO, new product. Data Process Governance·        Create and maintain localprocedures for creating and maintaining high quality data. ·        Develop and maintain datamaintenance procedures at the local site, including developing tools andtemplates to help others adhere to the standards with the local organization·        Defining and overseeing the datacollection process, including adherence to local quality system requirementsfor configuration/engineering change control.·        Collaborating with the MasterData Governance to ensure full knowledge of and compliance to Corporate dataquality standards·        Analyze and resolve data problemsthat may be causing downstream transactional issues·        Measuring and reporting on localdata quality·        Lead and participate to projectrelated to configuration and data management Requirements: ·        University Degree in IndustrialEngineering (preferred), Electrical Engineering, Information Systems, orComputer Science·        Minimum of 3-5 years’ experiencein Manufacturing/ Planning and Execution used in Manufacturing environment withgood understanding of processes, materials and flows.·        Preferably in Medical/ Pharmacontrolled environment.·        Hands-on work experience with invarious IT systems/ applications used in Manufacturing environment.·        Ability to learn the manufacturing processes/Bill of Materials/ Material requirements and to develop associated workflows. ·        Experience in managing changecontrol of such systems ·        Exceptional analytical andproblem solving skills ·        Experience with regulatorydocumentation and procedures QualitySystems Specialist Main Responsibilities:Responsibility Compliance of Quality System ·        Train QualitySystem users on the QMS processes and governance·        Be the focus pointfor all questions related to QMS ·        Liaise with theentities connected to Quality System for maintaining the compliance level·        Lead theharmonization of QMS to BU / corporate requirement ·        Involved in theQuality System Audit by external Notified Body and Agencies. ·        Perform internalaudit on QMS processes and provide support to the organization to improve theeffectiveness and efficiency of QMS processes. Deploy and MaintainQuality Metrics ·        Designorganization Quality Metrics for insuring a good monitoring of QMS efficiency·        Maintain QualityMetrics data·        CommunicateQuality Metrics to the Quality Management System Quality System ChangeManagement Process ·        Ensure that allQMS change are properly captured, reviewed, deployed and documented·        Liaise withRegulatory Affairs for communicating the necessary change notification·        Be the owner forthe standards surveillance. Trigger the applicable standards change in theorganization QMS Support / Coordinatethe Internal Audit, CAPA and Deviation Processes ·        Own & supportthe internal audit plan realization·        Train and supportend users on QMS processes·        Support & leadthe good CAPA process execution and escalate deviation to Quality management asrequired Requirements: ·        University Degree or Master or equivalentexperience.·        Have a quality certification or demonstrateequivalent experience in the Medical Device or Pharmaceutical industry.·        Minimum 2-3 years of experience inproject/team management on medium scope or background in product or processdevelopment projects. ·        Experience in the field of Pharmaceutical orMedical Device Industry and Quality Management System is an asset·        Desktop applications, analytical tools,presentations, document management·        Strong communication skills to participate inmulticultural and multi-departmental teams, and to lead a local technical team.·        Good communication skills with people fromall levels in the organization.·        Able to solve technical problems, autonomousand decision making abilities, requires minimal supervision·        Coaching skills to act as a local technologymentor. QAEngineer Main Responsibilities:·        Assurethat processes comply with specifications, Quality Systems Regulations and ISOstandards.·        Documentthat processes complies, with a high confidence level, the tolerances stated onthe product specification and drawings.·        Establishmechanism to evaluate, measure, monitor and/or quality in our products.·        Evaluateproduct/ material discrepancies. (PRB/MRB) on time, and implement correctiveactions accordant.·        Workon new product transfers and actively participate in the qualifications andvalidations of product/ equipment and processes.·        Providecheck and balance to manufacturing/system changes submitted by ManufacturingEngineers.·        Workon special projects assigned by Supervisor/ Manager.·        Supportmanufacturing activities by also participating on production meetings.·        Updatemanufacturing processes in order to reflect quality concepts and specificationrequirements.·        Applystatistical tools in order to assure that processes comply with thespecifications.·        Ensurecompliance to audit findings in a timely manner.·        Coordinatequalification and validation activities for all product and technologytransfers.·        Participateon internal quality audits by reading and understanding the audit plan, checklist, and performing initial meetings with auditor.  Participate in thegeneration of the written report of findings and in the wrap-up responses toassure corrective actions are implemented.·        Evaluate/approve engineering change requests/ orders.·        Conductfailure investigations in order to initiate, stimulate, and assign correctiveaction. Issue written reports and update, accordingly. Requirements: ·        Degreein Engineering.·        Minimum3 years of experience in Engineering related to manufacturing of small electro/mechanical devices preferably in a quality assurance or test related capacity.·        Goodcommunication and interpersonal skills with abilities to articulate ideasclearly and concisely to people of all levels. SeniorManufacturing Engineer Main Responsibilities: ·        Leading a team of Manufacturing Engineers and Technicians.·        Responsible for the support of Manufacturing Operations, improving theoperational standards, contribution in yield improvement and processcapability/performance.·        To lead and /or to participate in development,training, qualification and validation activities for product or technologytransfers.·        Monitors and improves goals and metrics established for company andarea of responsibility.·        To lead activities of Design for Manufacturability (DFM) andreliability.·        Ensurescompliance with company policies, programs, procedures, regarding to government and regulatory agenciesregulations (e.g. ISO, FDA, OSHA).  Ensure timely response to audit findings.·        Works withthe Manufacturing and Supply Chain teams to apply principles, concepts andtools for capacity projects and LeanSigma initiatives. ·        Works andimplements special improvement projects as assigned by Direct Supervisor. Requirements:·        Minimum 5years’ experience in Manufacturing Environment preferably in medical orelectronic devices including supervisory of Engineering team experience.·        Experience inLean Sigma Methodology and Continuous Improvements Programs.·        Excellent written reporting skills.·        Possessstrong knowledge and experience in the FDA regulated work environment.·        Experience inproject/team management or background in product/process development andproduct transfers projects.·        UniversityDegree in Engineering or related discipline. ManufacturingEngineer Main Responsibilities: ·        Responsible for the support of Manufacturing Operations,maintaining or improving the specified operational standards.·        Toprovide technical support to production personnel and manufacturing lines.·        Todevelop, update and revise manufacturing documentation following standards,internal policies and regulations established by regulatory agencies.·        To identify need, develop and provide adequate toolingand equipment to ease device manufacturability.·        Revises proposals for new product specifications orcurrent specification modifications established by design documentation.·        To initiate, evaluate, approve and implement EngineeringChange Order (ECR/ECO).·        To analyze and to determine conformance of materials andassemblies.·        Tolead and / or to participate in development,training, qualification and validation activities for product or technology transfers.·        Totrain production personnel, and other engineers/technicians.·        Monitors and improves goals and metrics established forcompany and area of responsibility.·        Ensurescompliance with company policies, programs, procedures, regarding to government and regulatory agenciesregulations (e.g. ISO, FDA, OSHA).  Ensure timely response to audit findings.·        Workswith the Manufacturing and Supply Chain teams to apply principles, concepts andtools for capacity projects and LeanSigma initiatives. ·        Worksand implements special projects as assigned by Direct Supervisor. Requirements:·        UniversityDegree in Engineering or related discipline.·        Minimum3 years’ experience in Manufacturing Environment preferably in medical orelectronic devices.·        Experiencein Lean Sigma Methodology and Continuous Improvements Programs.·        Good written reporting skills.·        Effectivecommunication skills. Technician(12 Hour Shift) Main Responsibilities: ·        SupportsQualification/Validation for product/process according to schedule and followup production until pass off requirement met.·        Supportsprocess improvement with IQ/OQ/PQ until pass off requirement met.·        Supports/participates to Development activities.·        Collaborateswith Transfer engineer and operation to evaluate, install, characterize,qualify and validate product/process/line in assigned scope of processes. ·        Collaborateswith Transfer engineer and operation to evaluate, characterize, qualify andvalidate major manufacturing and product improvements within performanceobjectives·        Followsand coordinates IQ/OQ/PQ activities on the lines.·        Trainsoperators and technical support of Implantable Device within IQ/OQ/PQactivities.·        SupportsImplantable Devices tasks (technical support, non-conformity management,continuous improvements·        SupportsOperation Excellence Initiatives                                                                                                                    Requirements:·        Diploma/ ITC / NTC in Engineering or equivalent·        Minimum 2 – 5 years relevant experience inequipment installation and maintenance in a manufacturing environment·        Good knowledge of mechanical, electrical,electronics, pneumatic and PLC ·        Experience in the application of theprotocols of validation and/or tests of validation produced. ·        Experiment in a medium of production,maintenance or breakdown service managed by a quality system·        Knowledge of Lean Manufacturing Software(office automation) ·        Familiar with MS Excel ·        Strongcommunication skills to participate in multicultural and multi-departmentalteams, and to lead a local technical team. ·        Ableto solve technical, logistic and human conflicts and problems.·        Coachingskills to act as a local technology mentor.你看下要是有合适的就准备你的简历，什么时候拿给我，我给你递去HR我也奇怪，那次明明看到有消息说有人回帖了，进去看没有东西。
谢谢了啊，看到了，只有这些职位么？老实说，不是特别吻合，不过有一个可以试试看你自己看吧，我是给不了什么意见了，要试的话，你准备你的简历给我就好了，我今晚去公司给你打印内推的FORM，到时候你填了那个，把简历一起给我，我星期一就可以给你递上去了那你的意思是，简历需要打印出来还是给你email过去？内推的form你怎么给我呢？我也要打印出来，FORM你得到我这填，方便的话，明天来淡宾尼，我家住这边，FORM我给你准备就是。方便留电话给我么？给我你的，我给你发短信
是pr没关系，就慢慢找吧，还是做相关行业比较好，经验不至于浪费
发送失败，发重了…应该过完年后比较好。大家这时候拿花红，都没那么快走吧~过个好年先过完年后职位应该会多些~现在大家都准备过新年和拿花红呢~等等吧想問樓主是那一行業~見了多時~
有時只要作出調整可能好快有工我是做半导体设备的，材料学背景。
我现在不是很挑剔了，半导体相关或者材料学相关的都投了，无奈还是没消息啊，面试都很少年肯定要过了，只不过过不好了而已
失业三个多月了，开始不淡定了找工作中，一起加油吧3月正式离职，想要去旅旅游，充充电，再考虑找工作的问题。有时候换个思路调整一下，也好过低着头一直瞎使劲。什么背景啊？羡慕啊工商管理还是相信船到桥头自然直吧，心态不那么急躁反而可能有的时候好运会来。我身边很多朋友都辞职了，基本都在1个月之内签到心水的offer。