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更新于 5月14日

研發(fā)實驗室管理崗

6000-8000元
  • 武漢江夏區(qū)
  • 3-5年
  • 本科
  • 全職
  • 招1人

職位描述

生物制藥醫(yī)療/生物生物工程醫(yī)療設(shè)備/器械
Job Responsibilities/崗位職責
1.Participate in the construction and maintenance of the R&D system, participate in the management of the R&D system. Assist the implementation of the R&D quality system.
參與研發(fā)體系的建設(shè)及維護;參與研發(fā)系統(tǒng)的管理;協(xié)助研發(fā)質(zhì)量體系的實施;
2.Report any finding in R&D lab management to CTO weekly, and plan the improvement as needed.
每周向CTO匯報研發(fā)實驗室管理工作中發(fā)現(xiàn)的問題,并提出整改措施;
3.Responsible for the management of the daily activities of R&D site, supervise the R&D site and its improvement, including on-site records, equipment management, daily maintenance, personnel operation, etc.
負責日常研制現(xiàn)場日?;顒拥墓芾恚瑢ρ邪l(fā)現(xiàn)場進行督察并監(jiān)督整改,包括現(xiàn)場記錄、設(shè)備管理、日常維護、人員操作等;
4.Responsible for the distribution and review of R&D original records. Responsible for R&D experimental notebook standardization, Audit the completeness, authenticity of all the data, and write the audit records and reports. Review the timeliness, authenticity, completeness of auxiliary records.
負責研發(fā)原始記錄的分發(fā)和審核管理;研發(fā)實驗記錄本規(guī)范性、完整性、數(shù)據(jù)真實性抽查,并形成記錄和報告;輔助記錄及時性、真實性、完整性抽查;
5.Responsible for the review process instruction, batch production records, quality standards, verification plans/reports, testing procedures, testing records/reports and other documents for R&D.
負責研發(fā)用工藝規(guī)程草案、部分批生產(chǎn)記錄、質(zhì)量標準、確認方案/報告、檢驗操作規(guī)程、檢驗記錄/報告等文件的審核;
6.Responsible for R&D material management, including purchasing, requisitioning, inventory,etc.
負責研發(fā)物料管理,包括采購、領(lǐng)用、庫存盤點等;
7.Training of R&D staff related to laboratory management.
對研發(fā)人員進行實驗室管理相關(guān)的培訓(xùn)工作;
8.Complete other tasks arranged by superiors.
完成上級安排的其他工作。
Job Requirements/崗位要求
1.Bachelor degree, science subject is preferred.
本科學歷,科學學科優(yōu)先考慮;
2.1-5 years of lab management industry experience, pharmaceutical or medical device experience is preferred. Those with quality management experience in biopharmaceutical are better.
1-5年實驗室管理行業(yè)經(jīng)驗,制藥或醫(yī)療器械經(jīng)驗優(yōu)先考慮。具備生物制藥質(zhì)量管理經(jīng)驗者更好;
3.Self-motivated, capable of handling independently, organizing and arranging multiple tasks, and able to perform under pressure and in line with the timeline.
有上進心,有能力獨立處理,組織和善于安排多項任務(wù),并能在壓力下執(zhí)行并符合時間線;
4.In-depth knowledge of GXPS and related guidelines and regulatory requirements.
熟悉GXPS和相關(guān)指南、法規(guī)要求;
5.Good oral and written communication skills in English and Mandarin, able to communicate effectively with other functional departments.
良好的英語和普通話口語和書寫交流能力,能有效與其他職能部門溝通。

工作地點

江夏區(qū)湖北省武漢市東湖開發(fā)區(qū)高新二路388號

職位發(fā)布者

Krystal Wang/hr

立即溝通
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