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Facility Validation Engineer 設(shè)施驗證工程師

1.7-2.5萬
  • 上海奉賢區(qū)
  • 5-10年
  • 本科
  • 全職
  • 招1人

雇員點評標(biāo)簽

  • 工作環(huán)境好
  • 同事很nice
  • 人際關(guān)系好
  • 氛圍活躍
  • 團隊執(zhí)行強
  • 交通便利

職位描述

GMP認(rèn)證EHS生產(chǎn)管理
工作內(nèi)容:
負(fù)責(zé)從設(shè)計到運營、放行、持續(xù)改進和退役的設(shè)施GMP設(shè)備和設(shè)施驗證生命周期的各個方面。
Responsible for all aspects of the Facility GMP equipment and facility validation lifecycle from design through operation, release, continuous improvement and retirement.
?負(fù)責(zé)廠房GMP設(shè)備/公用設(shè)施(例如純化水系統(tǒng),壓縮空氣系統(tǒng),環(huán)境監(jiān)視系統(tǒng))和受控工作環(huán)境(例如,潔凈室,倉庫)的調(diào)試與驗證工作
Responsible for commissioning and qualification of Facility GMP equipment/utilities (e.g. Purified Water System, Compressed Air System, Environment Monitoring System) and Control Work Environment (e.g. Clean Room, Warehouse)
?負(fù)責(zé)準(zhǔn)備驗證文件,包括但不限于驗證草案、風(fēng)險評估、定期審查。
Responsible for preparation of validation documentation such as but not limited to qualification protocols, risk assessments, periodic reviews.
?起草,審閱和批準(zhǔn)設(shè)備驗證所需的技術(shù)文件
Author, review and approve technical documents needed for qualification of equipment
?負(fù)責(zé)日常運營的廠房蟲害防治規(guī)程,管理蟲害供應(yīng)商,確保cGMP法規(guī)符合性。
Responsible for routine Pest Control procedure, vendor management and ensure cGMP regulatory compliance.
?負(fù)責(zé)日常運營的廠房設(shè)施儀表的校驗規(guī)程,管理校驗供應(yīng)商,確保cGMP法規(guī)符合性。
Responsible for routine Facility Instrument Calibration procedure, vendor management and ensure cGMP regulatory compliance.
?確保新/改進廠房設(shè)施設(shè)備或系統(tǒng)經(jīng)過正確的調(diào)試/驗證后交付投入運營
Ensures new/improvement facility equipment/system is appropriately commissioned/qualified and then handover for operational use.
?管理廠房設(shè)施工程團隊內(nèi)部的培訓(xùn),受控文件和圖紙的版本,變更控制,良好文檔實踐等
Provide governance and management for training, controlled document and drawings, change control, GDP within Facility team
?支持廠房設(shè)施年度預(yù)算管理包括成本節(jié)約項目,監(jiān)視季度花費的準(zhǔn)確性,確保公用設(shè)施和設(shè)備系統(tǒng)經(jīng)濟運營
Support Facility Annual Operation Cost Plan including cost VIP projects, monitor quarterly cost expense accuracy, ensure Lean operation
?與跨職能團隊合作,支持卓越運營,支持實現(xiàn)所有現(xiàn)場目標(biāo)
Collaborate with cross-functional team to support operational excellence and support achievement of all site objectives
?領(lǐng)導(dǎo)項目期間與GMP相關(guān)設(shè)備、設(shè)施和公用事業(yè)系統(tǒng)的調(diào)試與驗證等工作。
Leads the C&Q activities associated with GMP related equipment, facility and utility systems during project phase.
?參與所有中國藥監(jiān)和內(nèi)部對工廠的檢查與審計
Participates in all China GMP and internal audits of the manufacturing facilities
?保持質(zhì)量標(biāo)準(zhǔn),以滿足GMP要求以及公司內(nèi)部關(guān)于設(shè)備和系統(tǒng)的政策
Maintains quality standards to meet GMP requirements and internal company policies with respect to equipment and systems.
要求:
1. 專業(yè)知識Specific knowledge
?五年以上設(shè)施驗證工作經(jīng)驗 Minimum 5 years experience of validation for Facility system
?在潔凈空調(diào),潔凈室,潔凈公用設(shè)施系統(tǒng)方面擁有良好的專業(yè)知識 Good knowledge expertise in HVAC, Clean Room and Clean Utility.
?熟悉GMP,熟悉質(zhì)量控制流 Be familiar with GMP and quality control processes
?熟悉設(shè)備驗證標(biāo)準(zhǔn)、方法等 Be familiar with Equipment Qualification standard and methodologies
?熟練使用微軟辦公工具處理文檔(Word, Excel) Be familiar with Document handling using Microsoft (Word, Excel)

2. 個人(領(lǐng)導(dǎo)力)技能Personal and interpersonal skills / Leadership skills
?善于在不同組織間相互溝通和影響的能力 Good at interacting within different functions of the organization.
?關(guān)注于客戶和業(yè)務(wù)Focus on costumer and business
?有良好的團隊精神Good Team player
?誠實正直 Integrity
3. 個人態(tài)度和心態(tài)Personal attitude and mindset
?以創(chuàng)新和改變?yōu)轵?qū)動,保證競爭力Drives for innovation and change to ensure competitiveness
?樂觀進取的心態(tài),能夠在拔高的目標(biāo)和時限要求下敏捷,靈活性工作Can-do mentality, agility & flexibility able to work with stretched goals and deadlines
?愿意將團隊的目標(biāo)放在第一位并與團隊其他人一起朝著目標(biāo)努力Willing to place the goals of the team first and work with others towards these goals
?對相關(guān)專業(yè)活動有高度責(zé)任感Showing a high sense of responsibility regarding professional activities

4. 良好的醫(yī)療器械生產(chǎn)規(guī)范 Good Manufacturing Practice (GMP)
?堅持遵守GMP的程序Adhere to applicable GMP and procedures
?報告事件和偏差Report events and deviations.

5. 安全,健康和環(huán)境績效Safety, Health and Environment Performance
?堅持遵守EHS的程序Adhere to applicable EH&S and procedures
?報告事故,未遂事件及偏差Reporting of accidents, near miss and deviations
?配合和建議方案提高EHS程序Cooperate on and suggest solutions to improve EH&S
?當(dāng)看到違反EHS規(guī)則的行為要及時制止,做出適當(dāng)?shù)男袆印ct when violation of EH&S rules is observed and stimulate appropriate behavior

工作地點

奉賢區(qū)康希諾(上海)生物科技有限公司/

入職公司信息

  • 入職公司: 通用電氣醫(yī)療系統(tǒng)貿(mào)易發(fā)展(上海)有限公司
  • 公司地址: 上海浦東新區(qū)張江高科技園區(qū)華佗路1號2號樓通用電氣中國科技園1樓
  • 公司人數(shù): 1000-9999人

認(rèn)證資質(zhì)

  • 人力資源服務(wù)許可認(rèn)證

    人力資源服務(wù)許可證是由國家人力資源與社會保障相關(guān)部門頒發(fā),代表人才經(jīng)紀(jì)人所在企業(yè)可以合法開展人力資源相關(guān)業(yè)務(wù)的資質(zhì)證件。展示該標(biāo)簽代表該企業(yè)發(fā)布此職位時已上傳《人力資源服務(wù)許可證》或《人力資源服務(wù)備案證書》并經(jīng)由平臺審驗通過。

職位發(fā)布者

譚思琪/人事經(jīng)理

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北京外企德科人力資源服務(wù)上海有限公司(FESCO Adecco):官方網(wǎng)站:http://www.fescoadecco.com/北京外企德科人力資源服務(wù)上海有限公司(外企德科 FESCO Adecco)是值得客戶信賴的人力資源解決方案提供商和全球合作伙伴,是中國人力資源服務(wù)行業(yè)最具競爭力和品牌價值的FESCO(北京外企服務(wù)集團)與全球人力資源服務(wù)行業(yè)領(lǐng)航者The Adecco Group(德科集團)于2010年成立的一家中外合資人力資源服務(wù)企業(yè),為企業(yè)及個人提供業(yè)務(wù)外包、人事服務(wù)、招聘獵頭和員工福利等人力資源解決方案。目前,F(xiàn)ESCO Adecco在浙江、陜西、重慶、深圳、蘇州設(shè)立了分支機構(gòu),全國服務(wù)人數(shù)超過200萬名,服務(wù)客戶超20,000家。
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