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重慶博騰精細化工有限公司

招聘職位
·分析工程師
·API倉庫主管 API Warehouse Supervisor
·原料藥高級合成工程師
·物流專員 Logistic Specialist
·API 車間主任 API Workshop Manager
·API 生產總監 API Manufacturing Director
·儀表主管 Electrical&Control and Automation C
·技術主管 Technical supervisor
·化工區班長 Shift Supervisor
·潔凈區班長 Shift Supervisor
·QA工程師(QA Engineer)
·試車主管及工藝工程師Commissioning coordinator & P&
·工藝工程師(108項目) Process Engineer
·驗證主管及工藝工程師Validation coordinator & P&ID
·設備工程師(108項目) Equipment Engineer
·確認和設備工程師 Qualification & Equipment Engi
·設備主管(108項目) Equipment Coordinator
·確認和設備主管 Qualification Coordinator & Equi
·電氣工程師(一次回路) Electrical Engineer
·電氣工程師 Electrical Engineer
 
 重慶博騰精細化工有限公司
 工藝工程師(108項目) Process Engineer
職位類型: 工程生產類 薪金待遇: 面議
招聘部門: 招聘人數: 人數不限
發布日期: 2019-1-9 截止日期: 2019-12-31
工作地區: 重慶 現所在地: 不限
學歷要求: 大專 工作年限: 五年以上
年齡要求: 不限 性別要求: 不限

職位描述:
SPECIFIC RESPONSIBILITIES:
1. Responsible for collecting the information related to the process safety and quality;
2. Prepare the process relevant documents for EIA and safety pre-assessment;
3. Completing the equipment list and the equipment specification;
4. Taking part in selecting the equipment and technical negotiating;
5. Communicating with the design institute and preparing all the informations needed;
6. Taking part in the GMP review and evaluation of the project;
7. Taking part in the EHS review and evaluation of the project;
8. Responsible for PHA of the project and define the critical facilities and equipments of safety;
9. Responsible for organizing criticality analysis and define the critical parameter;
10. Responsible for organizing the impact assessment to the quality of the facilities and equipments. Define the critical facilities and equipment of quality;
11. Preparing the PFD and P&ID sketches;
12. Responsible for preparing validation master plan (about the process validation, analytical method validation and cleaning validation);
13. Cooperating with others to implement the commissioning and qualification;
14. Preparing the workshop manufacturing management procedures and process document;
15. Organizing the training for the workers before the validation;
16. Organizing the preparing of the validation protocol for process, analytical method, cleaning and computer system. And organizing the implementation of the validation;
17. Review the validation report;
18. Preparing the validation report regularly.

EDUCATION AND EXPERIENCE REQUIREMENTS:
1. Junior degree or above;
2. Above five year’s working experience and having taken part in the construction project of the Active Pharmaceutical Ingredients workshop or factory once or more;
3. Good coordination ability;
4. Good understanding the quality and the EHS requirements of the overseas related Active Pharmaceutical Ingredients project;

具體職責 Specific Responsibilities:
1、負責工藝安全和質量相關信息的收集;
1、編寫安評、環評等資料的工藝內容;
2、完成設備一覽表及設備規格要求;
3、參與設備選型及技術談判工作;
4、與設計院進行溝通,準備設計院所需資料;
5、參加建設項目的GMP審核和評估工作;
6、參加建設項目的EHS審核和評估工作;
7、負責建設項目的工藝安全評估,并確定安全關鍵設備及設施;
8、負責組織工藝關鍵性分析,確定關鍵工藝參數;
9、負責組織設備和設施對質量影響的評估,確定關鍵設備及設施;
10、制訂PFD和P&ID草圖;
11、負責編制驗證總計劃(工藝驗證、分析方法驗證和清潔驗證部分的總計劃);
12、配合進行設備確認和試車工作;
13、制訂車間生產管理文件及工藝文件;
14、組織車間員工的培訓工作;
15、組織編寫工藝、分析方法、清洗和計算機系統等驗證方案并組織驗證的實施;
16、定期編制驗證工作報告。

必備任職條件Desired Experience and Competency:
1、化工、制藥及相關專業,大專及以上學歷;
2、5年以上精細化工、醫藥工廠車間工段的生產管理或技術管理工作經歷;
3、熟悉GMP及藥品相關的法律法規;
4、具有良好的協調能力。

期望的任職條件Expected Experience and Competency:
1、參與1個及以上原料藥車間或工程的GMP認證;
2、了解國外有關原料藥項目的質量要求和EHS要求;
3、熟練的工程英語聽說讀寫能力,能夠與國外專家直接口頭或書面的溝通。

  
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重庆时时彩官方开奖