Job Information职位信息

Job title职位名称: Senior Technician, Purification 纯化高级技师

• Location工作地点： Shenzhen 深圳工厂
• % Remote working and % of travel expected 远程办公和出差的概率：2%
• Job type工作类型: Full time全职
• Site/Unit 区域/事业部：Shenzhen/ Flu Bulk Production深圳工厂/原液生产部

About the job工作职责

Our Team我们的团队：

Manufacturing & Supply consists of 3 manufacturing platforms based on global business units, as well as supporting functions of Quality, Market Supply and Strategy. We are committed to making best class medicines with excellent strategies and tools and delivering them to our patients.

制造与供应事业部包含以3个全球事业部为基础的制造平台，以及质量、供应商、精益战略等支持部门。致力于用优异的战略和工具制造优质的药品并传递到患者手中。

Main responsibilities职责描述：

Please indicate here the main job responsibilities请列举该职位的主要工作职责。

He take the charge of distribution, filtration, zonal centrifugation, and daily production organized, cleaning and disinfection, materials prepared, environment etc.  He ensure that quality rules and HSE rules are followed up during manufacturing operation of purification area, and performs production process in a safe and efficient manner.

负责完成相关接收、过滤、区带离心，以及日常组织生产、清洁消毒、物料准备和环境监控等,在纯化区域的生产运作中遵守质量守则及健康环境安全守则，确保生产安全有效地进行。

关键职责Key Accountabilities：

1、个人发展Personal development

• Focus on health, safety and environmental requirement of production, and make corresponding improvement and adjustment when necessary.
• 关注健康、安全及生产环境要求并在必要时作出相应改善及调整。
• Continuously improve the capability in production ability, deviation handled, environmental control, qualification and validation, HSE and so on.
• 持续提高个人在生产能力、偏差处理、变更控制、环境监控、确认与验证、HSE等方面的能力。
• Develop personal cross function and muti-skill Talent training.
• 发展个人交叉岗位及多技能人才培养。

 2、工作交付Work Delivery

• Attend production operations of purification area and delivery production with quality and quantity.
• 参与纯化区域的生产运作并按时按质按量交付产品。
• Ensure personal training and qualification on request; ensure materials supply and human arrangement.
• 根据要求确保个人的培训及资质；确保物料供应及人力调配。
• Ensure production activity according related process procedure, SOPs and BPR, fill and delivery record and BPR in time.
• 确保生产活动根据相关工艺规程，标准操作规程及批记录进行，按时填写和提交区域记录和批记录。
• Support/ input related production data in time. Resolve problem happened during production. Responsible for writing related technician document.
• 按时提供/录入相关生产数据；解决生产中出现的问题；负责相关技术文件的编写。

 3、质量系统实施Quality system implementation

• Handle, investigate deviation from production area.  Provide assessment for change control, CAPA and ER finished in time.
• 处理、调查生产领域中发生的偏差；根据实际情况提出变更控制，及时完成CAPA、ER。
• Assisted by related department and CI group,

 complete machine/equipment/calibration/qualification/validation activity.

• 在相关部门和持续改进组的协助下，按时完成规定的机器/设备/厂房的校准/确认/验证活动。
• Attend actively building’s GMP inspection, improve GMP compliance.
• 积极参与车间GMP自查，促进部门GMP合规性。
• Undertake Bulk production area supervisor’s related authorization responsibility, check and sign related GMP document.
• 承担原液生产部区域主管的相关授权职责，进行GMP相关文件审核和签名。
• Deliver appointed continuous improvement item and other job objective.
• 交付指定的持续改进项目或其他工作目标。

 4、实现目标、实施 公司价值观和文化Achieve the goal, implement company value and culture

• Break down department objective and assign to individual objective, delivery employee performance regularly, guide employee in time to implement company development direction.
• 分解部门目标并分派给各个体目标，定期提交员工绩效。
• Improve personal work positivity, strengthen department inner communication and cohesion, ensure to achieve work goal and high work efficiency.
• 提高个人工作积极性，加强部门内部沟通和凝聚力，以保证达到工作目标和最高工作效率。
• Obey the work arrangement of the department or the direct superior, and actively participate in the backup and transfer of different positions.
• 服从部门或直接上级工作安排，积极参与不同岗位的备份和转岗工作。

About you 任职资格:

List here ideally the must-haves criteria to be successful on the role.

请列出胜任该职位所必须具备的条件。

• Experience: More than 3 years of relevant work experience

工作经验: 3年以上相关工作经验

• Soft skill: Able to operate office software such as Word, Excel, etc. Able to write documents, processes and guidelines.

通用技能: 会操作办公软件，如word、Excel等。能撰写文档、流程和指引。

• Technical skill: Familiar with biochemistry, microbiology, virology, physical chemistry. Familiar with pharmaceutical regulations, such as GMP, etc.

专业技能: 熟悉生物化学、微生物学、病毒学、物理化学知识。熟悉制药法规，如GMP 等。

• Education: Full-time college degree or above

教育背景: 全日制专科以上学历

• Languages: The English level is average and can understand simple English documents.

语言要求: 英语水平一般，能看懂简单的英语文件。

Pursue progress, discover extraordinary进无止境，探索菲凡

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

进步，外部可见。更好的药物，更好的效果，更高的科学。但是进步离不开人去创造——来自不同背景、不同地区、担任不同岗位的人。所有人都团结在“创造奇迹的渴望”这一使命下。让我们成为这样的人。

在赛诺菲，不分种族、肤色、血统、宗教、性别、国籍、性取向、年龄、公民身份、婚姻状况、残疾或性别认同，我们为所有人提供平等的机会。

观看我们的 ALL IN 视频，并在 sanofi.com 网站上查看我们有关多元化、公平性、包容性的举措。