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发表于 2016-3-1 13:52:05
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杭州健康药物工厂
Position:：Drug Substance Operation
City:Hangzhou
Responsibility:
1. Provide local execution support during CTA lot execution at CROs/CMOs.
2. Lead execution of DS startup/scaleup/clinical lots production in new facility.
3. Author, review, and approve documentation such as batch records, procedures, and validation reports.
4. Collaborate cross-functionally with local and global team to troubleshoot/resolve issues and drive improvement.
5. Manage the DS team through the training, operations, performance etc.
6. Proactive and real-time RFT support of critical operations.
7. Communicate and resolve operational variances.
8. Process monitoring including real time review of process parameters and process data/trend analysis. Communicate process performance across shifts and departments.
9. Implement process enhancements, measure and respond to equipment capability and implement new technologies.
10. Provide input, review, and approval for investigations, commitments, and change controls to ensure changes are value added and processes and equipment are robust.
11. Perform skills training and provide subject matter expertise to training materials.
12. Promote a culture of Innovation and Continuous improvement. Drive changes that support Right First Time, Efficiency, and/or reduced costs.
13. Develop programs and strategies for real time process monitoring and right first time.
14. Provide Audit support as SME.
Qualification:
1. BS or MS in chemical engineering, biology, biochemistry or other related science or engineering field.
2. Familiarity and experience with mammalian cell culture, protein purification and/or solution formulation is not essential, but is highly desirable.
3. Previous experience in a GMP manufacturing environment desirable.
4. Previous experience with manufacturing-scale bioreactors/fermentors, centrifuge, column chromatography and/or tangential flow filtration (UF/DF) a plus.
5. Experience with Six Sigma, Method 1, 5S and/or other operational excellence programs a plus.
6. Enterprise Systemsfamiliaritypreferred, namely LabWare LIMS, SAP, TrackWise, PDOCS and EAMS.
7. Previous leadership skills a plus.
Position:：Drug Product Operation
City:Hangzhou
Responsibility:
1. Provide local execution support during CTA lot execution at CROs/CMOs.
2. Lead execution of DP startup/scaleup/clinical lots production in new facility.
3. Author, review, and approve documentation such as batch records, procedures, and validation reports.
4. Collaborate cross-functionally with local and global team to troubleshoot/resolve issues and drive improvement.
5. Manage the DP team through the training, operations, performance etc.
6. Proactive and real-time RFT support of critical operations.
7. Communicate and resolve operational variances.
8. Process monitoring including real time review of process parameters and process data/trend analysis. Communicate process performance across shifts and departments.
9. Implement process enhancements, measure and respond to equipment capability and implement new technologies.
10. Provide input, review, and approval for investigations, commitments, and change controls to ensure changes are value added and processes and equipment are robust.
11. Perform skills training and provide subject matter expertise to training materials.
12. Promote a culture of Innovation and Continuous improvement. Drive changes that support Right First Time, Efficiency, and/or reduced costs.
13. Develop programs and strategies for real time process monitoring and right first time.
14. Provide Audit support as SME.
15. Provide support to DS operation at startup and when needed.
Qualification:
1. BS or MS in chemical engineering, biology, biochemistry or other related science or engineering field.
2. Familiarity and experience with Asepticoperation, isolator, lyphilization andsolution formulation.
3. Previous experience in a GMP manufacturing environment desirable.
4. Previous experience with manufacturing-aseptic operation , autoclave, VHP, isolator and filling line, freeze drying and packaging. is highly desirable.
5. Experience with Six Sigma, Method 1, 5S and/or other operational excellence programs a plus.
6. Enterprise Systems familiarity preferred, namely LabWare LIMS, SAP, TrackWise, PDOCS and EAMS.
7. Previous leadership skills a plus.
健康药物业务
职位名称：Sales Intern-Hospital
工作职责：
1. 在销售主管的领导下完成销售指标及其他各项销售任务；
2. 根据拜访计划，定期拜访医生，药剂人员及相关目标人员，推广公司产品并与他们保持良好的合作伙伴关系；
3. 策划、组织多种形式的学术活动，宣传公司产品，并对学术活动加以跟进；
4. 积极收集医院及医药市场信息，特别是竞争对手信息并及时向主管反馈；
5. 建立区域内目标客户及竞争产品的相关档案，并及时完善增补；
6. 及时准确完成各项销售报告，并能有效利用；
7. 有计划地实施社区教育活动，建立社教网络，扩大社教人群。
职务要求：
1. 头脑灵活，性格外向；
2. 善于发现机会点，分析机会，并实现于销售；
3. 熟练的办公软件操作能力和谈判演讲能力；
4. 有优秀的客户沟通能力，在竞争环境中获得有利于公司的销售机会。
招聘城市：
浙江省：杭州市宁波市温州市
生物制药业务区域扩张团队
职位名称：医学信息沟通实习生
工作职责：
1. 全面了解辉瑞公司历史、文化及企业核心价值观；
2. 学习业务流程，熟悉产品推广模式，掌握相关专业知识；
3. 接受适当培训，跟随导师学习合规的工作方式以及了解学术推广活动的组织及收集市场信息的反馈的标准流程；
4. 熟悉辉瑞医学信息沟通专员的工作内容，学习幻灯片制作及业务数据收集、分析技巧，练习幻灯片演讲；
5. 了解公司的商业信息并根据辉瑞信息保密制度采取适当方式进行管理；
6. 在实习各个阶段随时接受学习成果的考核；
7. 在实习期间不会独立开展活动。
任职资格：
1. 2016届或2017届毕业生，专科及以上学历，专业不限；
2. 临床医学、药学及医药/生物相关专业优先；
3. 良好的沟通能力和较高的人际敏感度；
4. 良好的再学习能力和主动学习意愿；
5. 乐观积极，有一定的压力承受力；
6. 良好的团队合作精神；
7. 熟练使用MS Office。
招聘城市：
安徽省：歙县/南陵
福建省：福州周边龙岩市泉州市厦门周边漳州周边
广东省：潮州阳江湛江
广西壮族自治区：梧州
海南省：东方市
河北省：保定周边邯郸周边衡水周边廊坊周边石家庄周边 邢台周边张家口周边
河南省：开封市郑州周边
黑龙江省：哈尔滨周边
湖北省：京山利川南漳潜江浠水应城
湖南省：长沙周边
吉林省：长春周边
辽宁省：沈阳周边
内蒙古自治区：赤峰周边
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发表于 2016-3-1 13:51:19
