www.bhdu.cn-夜肉伦伦影院无码 ,国产精品www夜色视频,3d动漫精品啪啪一区二区免费,久久婷婷综合缴情亚洲狠狠

<blockquote id="4uc0g"><tfoot id="4uc0g"></tfoot></blockquote>
  • <fieldset id="4uc0g"><table id="4uc0g"></table></fieldset>
  • <fieldset id="4uc0g"><menu id="4uc0g"></menu></fieldset>
  • <ul id="4uc0g"><sup id="4uc0g"></sup></ul>
    <strike id="4uc0g"></strike>
    <del id="4uc0g"></del>
    <strike id="4uc0g"></strike>
    更新于 今天

    實(shí)驗(yàn)室QA/Lab QA

    8千-1萬
    • 南通啟東市
    • 1-3年
    • 大專
    • 全職
    • 招5人

    職位描述

    QA檢驗(yàn)QA審核

    1.Review
    laboratory controls before release of raw materials/ excipients/ packaging
    materials/ finished product. Ensure any errors or deviations have been fully
    investigated and acted upon as appropriate. 對(duì)原料/輔料/包裝材料/成品進(jìn)行放行前審核。確保對(duì)任何錯(cuò)誤或偏差進(jìn)行充分的調(diào)查并采取適當(dāng)?shù)男袆?dòng)。


    2.To
    release or rejected raw materials/ excipients/ packaging materials/ finished
    product.

    放行或拒絕原料/ 輔料/ 包裝材料/ 成品。

    1. To
    ensure that all OOS/OOT/OOAL/OOAC of laboratory have been investigated and
    handled timely.


    確保所有OOS/OOT/OOAL/OOAC已經(jīng)過調(diào)查并得到及時(shí)處理。


    2. Maintenance
    Deviation handling system. Coordinate risk assessment for deviation and
    review corrective actions for deviation. Ensure close deviation in time.


    維護(hù)偏差處理系統(tǒng)。協(xié)調(diào)偏差風(fēng)險(xiǎn)評(píng)估,審查偏差糾正措施。確保及時(shí)關(guān)閉偏差。


    3. Maintenance
    CAPA system. Follow up CAPA status. Ensure close CAPA in time.


    維護(hù)CAPA系統(tǒng),跟蹤C(jī)APA狀態(tài)。確保及時(shí)關(guān)閉CAPA.


    4. To review
    the change controls related to the quality control.


    審核關(guān)于QC的變更。


    5.
    Control
    Documents and records, ensure effective version for QC and MICRO.


    正確及時(shí)有效地執(zhí)行對(duì)文件的管理以保證和理化和微生物實(shí)驗(yàn)室使用正確的文件和記錄。


    6.
    Issue QMS number and documents, maintain the logbooks,
    and finish the trend of non-conforming events every year.


    發(fā)放QMS文件編號(hào)和文件,維護(hù)臺(tái)賬,每年進(jìn)行不符合事件的趨勢(shì)回顧分析。


    1.Review laboratory documentation
    such as test records, audit trail, electronic data, analytical methods, specifications, SOPs and Non-conformity
    investigation reports to ensure compliance.


    對(duì)實(shí)驗(yàn)室文件,如測(cè)試記錄,審計(jì)追蹤,電子數(shù)據(jù),分析方法,質(zhì)量標(biāo)準(zhǔn),SOP,不符合項(xiàng)調(diào)查報(bào)告等進(jìn)行審核,確保文件的合規(guī)性。


    2. Follow up all instrument calibration plan,
    maintenance plan, water sampling plan, environmental monitoring plan, gas
    detection plan, dressing qualification verification plan, clock calibration
    plan, stability sampling plan, etc., to ensure that the activities are
    completed as planned and on time.


    跟蹤所有儀器校驗(yàn)計(jì)劃、維保計(jì)劃、水的取樣計(jì)劃、環(huán)境監(jiān)控計(jì)劃、氣體檢測(cè)計(jì)劃、更衣資質(zhì)確認(rèn)計(jì)劃、時(shí)鐘校準(zhǔn)計(jì)劃、穩(wěn)定性取樣計(jì)劃等,確保活動(dòng)按計(jì)劃按時(shí)完成。



    工作地點(diǎn)

    江蘇西普拉制藥有限公司

    職位發(fā)布者

    冒女士/HR

    今日活躍
    立即溝通
    江蘇西普拉制藥有限公司
    江蘇西普拉制藥有限公司。成立于2019年8月8日。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。
    公司主頁
    久久久国产精品无码免费专区| 久久久久精品国产亚洲AV| 国产精品亚洲综合天堂夜夜| 少女韩国电视剧在线观看完整| 少妇真人直播app| 久久国产精品99精品国产| 精品第一国产综合精品aⅴ| 神马影院在线观看| 亚洲天堂在线观看| 国产精品亚洲欧美日韩精品白浆高清|