2012罗氏制药招聘

Associate, Rocephin, Production 专员，罗氏芬，生产

Organize the production in Rocephin area, including the stages of preparation, filling, and visual inspection, cleaning and sterilizing equipments and environment according to SOPs to ensure the all productions are high quality on the basis of GMP.
Support supervisor to organize and manage the team of sterile production , integrate all kinds of resources necessary to ensure the smooth process in sterile production. To make sure that the process is run under fully GMP and Safety control.
在罗氏芬车间组织生产。负责罗氏芬整个生产工序，包括准备，灌装，目检阶段，根据SOP对设备和环境进行清洁和消毒。确保在GMP的基础上生产出高质量的产品。
帮助主管对区域人员进行管理，整合资源保证生产顺利进行，同时确保整个流程是安全的同时是符合GMP的。

Primary responsibility
1.Organize and manage the production in his or her responsible area
对负责区域人员的组织和管理
By assisting the his or her supervisor to consider capacity of facility and equipment , labor force and production cost make weekly plan for sterile production area to meet requirement of sales
协助上级对设备产能，劳动力及生产成本进行评估，确保销售需求。
Monitor line performance; achieve daily/weekly production targets
生产线监督，保质保量完成每日/每周生产目标。

2.GMP and safety surveillance
GMP 和安全监督
Through assisting his or her superior, lead team to implement cGMP standard in the production with supervision in order to guarantee the quality of products and performance in international standards. To ensure safe operation protection in daily work based on national or company’s policy.
协助上级带领并监督区域人员在生产时实施GMP标准，以保证产品质量和人员操作符合国际标准，根据国家或公司的政策确保日常的安全操作保护措施。
Involve in the investigation of the defects during the manufacturing, follow up the implementation of action plan
参与调查生产过程中的偏差，跟进行动计划的执行

3.Document
文件
Check and review the documentation on site such as batch document, logbook are filled in accordance with regulatory requirements timely.
及时检查并确保现场文件如批记录、日志的填写符合规范。
Support his or her superior to build a professional team
协助上级建立一个专业队伍
By cooperating with his or her Superior , develop and train his or her subordinate to enhance GMP awareness , professional skill and capability . Follow up the team members’ training schedule.
与上级合作，发展和培训下属以加强GMP意识，专业技能和个人能力。跟进下属培训进程。

4.Process improvement and organize process Validation
工艺改进及工艺验证
Assistant supervisor optimize the process through parameter perfecting mechanical adjustment of machine and etc, to achieve material localization, increase the quality and have been better output .
Assistant supervisor plan and Implement the process validation to guarantee the quality stability of the changed process.
协助主管通过调整运行参数及设备参数进而优化工艺流程，以提高产品质量。协助主管计划并实施工艺验证以确保变更工艺后可获得质量稳定的产品。

Requirements
Bachelor degree or above.Pharmaceutical technology or relevant fields
本科以上学历，药学或相关专业
At least 1 year related experience in pharmaceutical company
至少1年制药厂的工作经验
PC skill Knowledge of pharmaceuticals
电脑操作具有制药方面的知识
Able to take 3 shifts
能够倒3班

Please send your resume to: mary.meng@roche.com

2011毕业生可接受，已有一位2011毕业生被录用，因班次安排还需增加一人，欢迎加入罗氏！

上海罗氏制药有限公司是全球十大制药企业之一的瑞士罗氏集团在中国建立的第一家合资企业，提供肿瘤学、病毒学、移植学等各类关键治疗领域的各种处方药，努力从根本上改善人们的生活质量。上海罗氏所有生产线都通过GMP认证，2005 年10 月致敏生产基地在张江厂区落成。