中国僵尸片,亚洲欧美国产另类视频,亚洲精品无码人妻无码,亚洲有码转帖,亚洲欧美精品伊人久久,97精品依人久久久

更新于 6月3日

研發(fā)質(zhì)量保證專員

5000-7000元
  • 武漢江夏區(qū)
  • 1-3年
  • 本科
  • 全職
  • 招1人

職位描述

GMP認(rèn)證
1. Responsible for establishing and managing the R&D quality management system. Responsible for the management of the R&D file system. supervising the implementation of R&D system files, and forming records and reports; 負(fù)責(zé)建立和管理研發(fā)質(zhì)量管理體系;負(fù)責(zé)研發(fā)文件系統(tǒng)的管理;監(jiān)督研發(fā)體系文件的執(zhí)行情況,并形成記錄和報(bào)告; 2. Responsible for the review of process study protocols/reports, risk assessment report, batch production records, analytical method procedure, analytical method development protocols/ reports, stability study protocol/report and other documents for R&D; 負(fù)責(zé)研發(fā)工藝研究方案/報(bào)告、風(fēng)險(xiǎn)評(píng)估報(bào)告、批生產(chǎn)記錄、分析方法規(guī)程、分析方法開(kāi)發(fā)方案/報(bào)告、穩(wěn)定性研究方案/報(bào)告等文件的審核; 3. Responsible for the review and management of the R&D original records. Random checks on the standardization, completeness, and data authenticity of the R&D experiment records, and the formation of records and reports. Random checks on the timeliness, authenticity, and completeness of the R&D auxiliary records; 負(fù)責(zé)研發(fā)原始記錄的審核、管理;研發(fā)實(shí)驗(yàn)記錄規(guī)范性、完整性、數(shù)據(jù)真實(shí)性抽查,并形成記錄和報(bào)告;研發(fā)輔助記錄及時(shí)性、真實(shí)性、完整性抽查; 4. Responsible for carrying out quality management education and training, and regularly update and maintain the training matrix and training records of the R&D department; 負(fù)責(zé)開(kāi)展質(zhì)量管理的教育和培訓(xùn),定期更新和維護(hù)研發(fā)部門的培訓(xùn)矩陣和培訓(xùn)記錄; 5. Responsible for the quality management of the R&D, including quality requirements such as data management, deviation management, change management, CAPA management, risk control and evaluation; 負(fù)責(zé)研制過(guò)程的質(zhì)量管理,包括數(shù)據(jù)管理、偏差管理、變更管理、CAPA管理、風(fēng)險(xiǎn)控制與評(píng)估等質(zhì)量要求; 6. Responsible for participating in quality audits related to the R&D department, and supervising the rectification and tracking of observations; 負(fù)責(zé)參與研發(fā)部門相關(guān)的質(zhì)量審計(jì),并督促缺陷項(xiàng)的整改追蹤; 7. Responsible for suppliers’ management; 負(fù)責(zé)研發(fā)供應(yīng)商的管理; 8. Regularly organize and carry out R&D quality system review, responsible for continuous improvement of the quality system; 定期組織開(kāi)展研發(fā)質(zhì)量體系評(píng)審,負(fù)責(zé)質(zhì)量體系的持續(xù)改進(jìn); 9. Complete other tasks arranged by superiors. 完成上級(jí)安排的其他工作。

工作地點(diǎn)

江夏區(qū)武漢市東湖新技術(shù)開(kāi)發(fā)區(qū)光谷生物城高新二路388號(hào)

職位發(fā)布者

陳女士/HR

今日活躍
立即溝通
公司Logo鼎康(武漢)生物醫(yī)藥有限公司
鼎康生物是一家領(lǐng)先的CDMO公司,可提供一站式的CMC解決方案,支持從早期藥物開(kāi)發(fā)到后期臨床研究和商業(yè)化cGMP生產(chǎn)。鼎康引進(jìn)了全球首個(gè)模塊化生物制藥工廠Kubio;為客戶開(kāi)發(fā)的多個(gè)產(chǎn)品已經(jīng)在全球20多個(gè)國(guó)家進(jìn)行臨床試驗(yàn)。在不久的將來(lái),鼎康生物總產(chǎn)能將超過(guò)140,000L。我們承諾通過(guò)技術(shù)和生產(chǎn)創(chuàng)新,使全球患者都能負(fù)擔(dān)得起具有國(guó)際標(biāo)準(zhǔn)的生物藥物,提高治療水平以改善人類健康。
公司主頁(yè)