南京招聘

职位描述：
1.Artwork Related：
  画稿相关：
   1.1 Overall coordinator artwork design & modification for SASS/BMS China printed packaging components.
         总协调SASS/BMS China印刷包装材料画稿制作与修改
   1.2. Provide possible solution for printed packaging components for new product launching.
          为新产品上市提供印刷包装材料的相关解决方案
   1.3. Participate Global Artwork Development Project to improve and globalize artwork procedure.
          参与全球画稿进展项目，协助改善并使画稿流程全球化
   1.4. Help to make team decision for contingencies for artwork related issue and make adjustment as needed.
         帮助团队对画稿相关应急事件做出决定并按需做出调整
   1.5. Responsible for managing outside artwork developer.
         负责画稿外部供应商的管理
   1.6. Communicate with printing components vendors on technical field.
         在技术层面与印刷品供应商进行沟通
   1.7. Provide relevant supports for artwork revision to departments inside TO, including Eng. Department, Supply Chain and QA.
         为TO内部相关部门提供画稿相关的支持，包括生产工程部、物控部和质量部
   1.8. Provide relevant supports for artwork revision to departments outside TO, including Commercial Departments, GRS, Government Affair Department and Medical Affairs Department.
          为TO 外部相关部门提供画稿相关的支持，包括市场部、法规注册部、政府事务部和医学部
    1.9. Notice D&SO about packaging material change information for finished products.
         通知商务部成品包装变化信息
2.Anti-Counterfeit Related:
   防伪相关：
    2.1. Have the capability to identify counterfeit product
          有鉴别假冒产品的能力
    2.2. Identify both company & individual samples from Customer Service Department.
          负责客户服务部来自单位或个人的样品鉴定
    2.3. Work closely with EMEA/ AP Quality and Compliance for EMEA and AP market action fact-finding in the field of counterfeit product.
          与EMEA/亚太质量和保证人员在假冒产品领域就EMEA/亚太市场实际行为发现进行紧密合作
 2.4. Communicate with printing components vendors on the field of Anti-counterfeiting technology.
          与印刷品供应商就防伪技术进行沟通
3.Packaging Related:
   包装相关：
   3.1. Draft packaging line PQ validation protocol.
         制定包装线PQ验证方案
   3.2. Communicate with Manufacture Department and Planning Department to determine time for packaging line & production validation.
         与生产部及计划部沟通确定包装线及产品验证的时间
   3.3. Guide operators to operate and record according to PQ protocol.
          指导操作人员按照PQ方案进行操作和记录
   3.4. Finish packaging line PQ validation report, make sure it is approved by all related departments.
         完成包装线PQ验证报告，并确保所有相关部门均已批准
  3.5. Notice PQ result to related departments.
         将PQ结果通知相关部门
   3.6. Provide pre-support for new packaging line
         为新包装线引进提供前期支持
   3.7. Consider CI program for package operation.
         考虑包装操作的进一步方案
 4.Drug Serialization Related:
   药监码相关：
   4.1.Communicate with system aggregation vendor and printing material vendors to ensure robustness and reliability of Drug
         Serialization System in SASS.
        与系统集成商及印刷材料供应商沟通确保SASS的药监码系统强大及可靠
   4.2.Provide technical support for Drug Serialization System.
         对药监码系统提供技术支持
   4.3.Update China drug serialization status to HQ.
        向总部提供中国药监码状况更新
   4.4.Communicate with SFDA for drug serialization related work
       就药监码相关内容与SFDA沟通
   4.5.Keep close communication with D& SO and GRS for updating information about drug serialization.
        与商务部及法规注册部保持紧密联系，及时更新药监码最新信息
5.Complete other assignments given by superior.
    完成领导其他交办任务
1.Knowldge of GMP understanding
   熟悉理解“药品生产质量管理规范”
2.Have an excellent ability to listen, speak, read and write in both English and Chinese
   具有良好的中英文听说读写能力
1.Ability to use MS Office.
   具备使用办公室软件的能力
2.Ability to identify counterfeit product
   具备鉴别假冒产品的能力
3.Ability of effectively communicate and work with diverse members of the organization.
   具备能与公司内其他部门协调、合作，确保工作顺利进行的能力 举报 分享

百时美施贵宝是一家以“研发并提供创新药物，帮助患者战胜严重疾病”为使命的全球性生物制药公司。

2019年11月20日，百时美施贵宝成功完成了对新基的收购，将双方在领先的科学、创新的药物和优秀的人才等方面的优势合二为一，打造全球领先的生物制药企业。公司在肿瘤、血液、免疫和心血管疾病等领域处于世界前列，并具有丰富的，且具有行业前景的产品管线。

如今，中国已是百时美施贵宝公司全球重要的研发、生产、营销和创新中心之一。我们致力于满足中国未被满足的迫切的重大疾病需求，引领行业发展，开展多元合作，以帮助中国患者战胜严重疾病。