北京招聘

The Position


To be the position holder, you job is to support manager to organize and manage the manufacturing in solid manufacturing area, integrate all kinds of resources necessary to ensure the smooth process in production. You will need to make sure the process is run under full GMP and Safety control. Establish the SOPs, Batch records as well as other documents related to the production. In addition, you are also responsible for the quality of product of each batch. The details are listed as below.

岗位简介：协助生产经理组织固体制造区域的生产，整合各种资源确保生产的正常进行。确保GMP的实施以及安全操作。建立SOP，批次记录以及其他生产相关文件。同时应对每批产品的质量负责，具体工作职责如下：

1. Assume the roles and responsibilities / accountabilities of solid production manager during his/her absence.
在固体生产经理不在的情况下，承担生产经理的职责。

2. Organize and manage the production in Solid manufacturing, taking responsibility of problem solving and prevention on site, with knowledge of LP and HP manufacturing.
具有高活性与低活性固体制造的经验，组织并管理固体制造主车间，负责现场问题的处理及预防。

3. Taking responsibility of GMP documentation work of solid manufacturing area, including SOP, Quality system documents, Validation system documents, etc.
负责固体制造区域的相关GMP文件工作。包括SOP，质量体系文件，验证系统文件等。

4. Develop subordinates, including job rotation and cross function training.
负责部门内人员的发展。包括轮岗及交叉功能区域培训。

5. Consider capacity of facility and equipment, labor force and production cost, make weekly plan for solid manufacturing to meet requirement of sales.
对设备产能，劳动力及生产成本进行评估，制定周计划，确保销售需求。

6. Participate in / organize execution of process/cleaning validation
参与并组织工艺/清洁验证的执行步骤。

7. By optimizing the process through some parameter perfecting, mechanical adjustment of machine and etc, to achieve material localization, increase the quality and have been better output. Execute the process validation to guarantee the quality stability of the changed process.
通过调整运行参数及设备参数进而优化工艺流程，以获得物料本地化，提高产品质量。执行工艺验证以确保变更工艺后可获得质量稳定的产品。

8. Responsible for quality matters in solid manufacturing GMP and safety responsibility in solid manufacturing area
固体制造区域GMP及安全职责

9. Lead solid manufacturing to implement cGMP in order to guarantee the quality of products and performance according to international standards. By reinforcing and monitoring obedience to national and company’s regulation or policy, take care of safe operation protection in daily work.
对固体制造区域贯彻cGMP，以确保按照国际标准生产出高质量的产品。通过加强国家及公司内部制度和政策的实施，确保日程工作中的安全操作。

10. Build a Professional team
建立职业化的团队

11. Develop and train his or her subordinates to enhance GMP awareness, professional skill and capability.
对下属进行培训以提高GMP意识，职业技能和能力。

12. Participate in the respective projects in the solid production
参与固体制造区域的相关项目

13. Participate in and support the projects in solid production area including but not limited to IQ, OQ, PQ, etc. with high independency and competence.
参与并独立支持固体制造区域的相关项目，包括但不限于IQ，OQ，PQ等确认阶段。

14. Execute the projects and implement the projects in solid production.
执行固体制造区域的项目并运用项目结果。

15. Facilitate risk management/BPM and other process improvement within solid manufacturing.
在固体制造区域协助风险评估、BPM及其它流程改进。

16. System operationRelated SAP, MES and CHRIS system operation.
系统操作进行SAP，MES和CHRIS系统的相关操作。



Who you are

You’re someone who wants to influence your own development. You’re looking for a company where you have the opportunity to pursue your interests across functions and geographies. Where a job title is not considered the final definition of who you are, but the starting point.


To be the successful applicant, you hold a Bachelor degree or above, with pharmaceutical technology or relevant majors. You have 3 years’ experience in Pharmaceutical industry with 2 years’ experience in pharmaceutical manufacturing. You possess strong ability in organization and coordination, also you have strong sense of GMP. It would be desired if you have good team management skill as well as professional knowledge of pharmaceuticals. It would be a plus if your English language skill is good.

任职要求：
1. 本科及以上, 药学或相关专业
2. 3年制药企业工作经验,2年制药生产经验
3. 较强组织协调能力
4. 较强GMP意识
5. 良好的团队管理能力
6. 制药相关知识
7. 语言能力－英文&中文

The next step is yours. To apply today, click on the "Apply online" button below.


Who we are

At Roche, 88,500 people across 150 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity.

Roche China consists of Roche Pharmaceuticals and Roche Diagnostics, with more than 7,000 employees. While working to develop itself into Roche’s third global strategic centre, Roche China is also making sustained efforts to fulfill its long-term commitment to China.

Roche is an equal opportunity employer and strictly prohibits unlawful discrimination based upon an individual’s race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry,

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上海罗氏制药有限公司成立于1994年，是抗肿瘤、抗病毒、移植等关键领域的市场领导者。在大型跨国药企中，我们率先在中国建成了包括研究、开发、生产、营销等环节在内的完整的医药价值产业链。罗氏中国正向着成为罗氏全球第三个战略中心的目标迈进，以实际行动践行在中国长期发展的承诺。

我们始终以患者为中心，致力于帮助患者从根本上延长生命和改善生活质量。目前，罗氏在华拥有16个产品，覆盖8个治疗领域。我们与政府、医疗机构以及非政府组织等社会各界多方携手，共同探索创新的合作模式，通过一系列有影响力和可持续的举措惠及更多的中国患者。

更多罗氏中国信息，请登陆罗氏官网或访问罗氏招聘公众号。