執(zhí)行總監(jiān)的主要職責(zé)5篇(編輯修改稿)
2024-09-02 10:21 本頁(yè)面
【文章內(nèi)容簡(jiǎn)介】 urification), scale up, and tech transfer 熟悉工藝開發(fā)流程，技術(shù)轉(zhuǎn)移，后期工藝表征與驗(yàn)證 , 分析方法確認(rèn)與驗(yàn)證 Familiar with process development, tech transfer, late phase process characterization and validation, analytical method verification and validation Ability to handle multiple tasks at the same time, prioritize, and plete tasks within tight timeline. Anticipate plex technical issues and proactively develops practical solutions, proven ability to develop novel processes Demonstrate ability to make sound remendation and identify potential impacts to management 生物制藥行業(yè) 15 年以上制藥經(jīng)驗(yàn)并至少 5 年管理經(jīng)驗(yàn) At least 15 years of practical experience in Biopharmaceutical industry with at least 5 years of managerial experiences 英語(yǔ)水平優(yōu)秀，會(huì)熟練使用電腦 Fluent in English and Chinese， familiar with puter and Office system. 篇三 職責(zé)： 1. 在 VP 或總監(jiān)的領(lǐng)導(dǎo)下，負(fù)責(zé)發(fā)展與執(zhí)行指定項(xiàng)目的全球注冊(cè)策略，包括規(guī)范和非規(guī)范市場(chǎng) )。 2. 領(lǐng) 導(dǎo) (總監(jiān) )或參與領(lǐng)導(dǎo) (副總監(jiān) )國(guó)際注冊(cè)部或項(xiàng)目小組。作為注冊(cè)部的聯(lián)絡(luò)人，與外部合作伙伴及內(nèi)部職能部門進(jìn)行溝通聯(lián)絡(luò) 。 3. 負(fù)責(zé)產(chǎn)品開發(fā)及生命周期中國(guó)際注冊(cè)相關(guān)工作的管理及執(zhí)行
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