Manufacturing and Supply
Wo Wunder
der Wissenschaft
für Patient*innen
Realität werden

Job Information职位信息

Job title职位名称: Micro Specialist 微生物分析师

•    Location工作地点： Beijing, China 中国北京
•    % Remote working and % of travel expected 远程办公和出差的概率：5%
•    Job type工作类型: Full time全职
•    Site/Unit 区域/事业部：Beijing Site/ M&S China北京工厂/中国制造与供应事业部 
•    Solid Line Manager(Job Title and Name) ：Microbiology Supervisor Yanxia 直线汇报上级（职位名称+姓名）：微生物实验室主管 闫夏
•    Dotted Line Manager(Job Titel and Name): NA 虚线汇报上级（职位名称+姓名）：无

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：
1.    To carry out Sampling, Analytical testing and Reporting of API, raw materials, active ingredients, packaging materials, in process samples, intermediates, finished products and, as well as the monitoring of utility and environment  according to the test methods GMP requirements. 
按照分析方法和GMP的要求进行原辅料、包材、中控样品，以及成品的取样，微生物相关检验及报告。执行公用工程介质和环境监控；
2.    To Ensure that analyses are carried out on time and are in compliance with the specifications. Participate to the OOS investigations and the quality assessment.
确保样品及时检验并符合质量标准的要求。参与超标结果的调查以及产品质量评估；
3.    Perform analytical transferring / validation for the new products.
微生物分析方法转移及验证；
4.    To assist writing draft sops, draft qualification protocols of the analytical instruments and the analytical methods. Assist perform the qualification work.
协助编写微生物相关标准操作规程、仪器确认方案及分析方法。协助进行验证工作。
5.    To be the back up of the other analysts to achive the team target. 
其它分析员缺席时，作为替补以完成团队目标。
6.    Be engaged in the lab continuousely improvement for technical and management perpurse. Advocate and execute the sms concept and practice.
参与实验室管理及技术的持续改善活动。倡导和实施赛诺菲管理系统。
7.    Responsible help the supervisor for lab investigation and trouble shooting.
协助实验室主管负责实验室调查和问题的解决。
8.    Support new project preformed in the lab.
支持新的项目在实验室的执行。
9.    Quality Department HSE Responsibilities质量部HSE职责
-    Responsible for following the company’s HSE policy, and integrated all requires into daily job.
负责贯彻公司HSE的有关规定，把公司HSE制度的措施贯彻到每个具体环节。
-    Incorporate HSE work into the work plan
将HSE工作纳入工作计划中。
-    Organize the implementation of HSE management target plan of this department, implement HSE rules and regulations, HSE operation procedures and HSE technical action plan.
组织实施本部门HSE管理目标计划，落实HSE规章制度、HSE操作规程和HSE技术措施计划。
-    Regularly carry out to identify HSE potential hazards and develop action plan and finish on time.
定期开展本部门HSE隐患排查治理工作，制定整改计划并按时完成隐患整改。
-    Timely working out of employee opinions.
负责部门级HSE教育与考核工作；及时处理员工提出的意见。
-    Actively cooperate with HSE management to prevent accidents happens.
积极配合HSE管理工作，防止各类事故的发生。
-    Regularly carry out +QDCI meetings at all levels considering HSE8 requirements. Feedback HSE issues in a timely and accurate manner, and actively implement remediation.
定期开展本部门各级+QDCI会议，结合HSE8要求，及时、正确填写和反馈各类HSE问题，并积极落实整改。
-    Participate in the investigation for accidents, analyze the root causes of accidents from the quality management perspective, and related CAPA.
参加事故调查分析工作，从质量管理角度分析事故原因，提出事故防范措施。
-    Responsible for design annual department PASS plan, and ensure implementation as planned.
负责制定年度部门PASS计划，并按进度组织实施。
10.    Sanofi (Beijing) Pharmaceutical Co., Ltd. Energy Policy: "Quality as the top priority, through technical, behavioral, human consciousness, continuously reduce the rate of energy consumption in product value, benefit the users, and promote company development". Good awareness of energy conservation is required, participate in energy saving actions, and assist in the continuous development of the energy management system.
赛诺菲（北京）制药有限公司能源方针：“以药品质量为第一要务，通过技术手段，行为规范，人为意识，不断降低产品价值中的能耗比重，造福广大用户，促进企业发展”要求每位员工具有良好的节能意识，积极的节能行动，协助能源管理体系的持续开展

About you 任职资格:
•    Experience: At least one year of GMP-related work experience
工作经验: 有至少一年GMP相关工作经验
•    Education: 
教育背景: 药学、化学、生物、食品相关专业本科及以上
•    Languages: 
语言要求: 良好的英语听说读写能力优先
•    Play to Win Behaviors: Stretch; Take Action; Act for Patients & Customers; Think One Sanofi
全力致胜行为: 超越自我, 主动出击, 以患者和客户为本, 团结一致

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。
Take The Lead Behaviours：Aim Higher、Act for Patients、Be Bold and Lead Together
引领前行行为：更高目标、以患者为本、勇于创新、共同领导

Pursue Progress. Discovery Extraordinary.

Werde Teil von Sanofi und starte mit uns in eine neue Ära der Wissenschaft – wo dein persönliches Wachstum genauso wegweisend ist wie unsere Arbeit. Wir investieren in dich, damit du weiterkommst, schneller denkst und Dinge möglich machst, die vorher undenkbar waren. Du wirst Grenzen verschieben, Gewohntes hinterfragen und smarte Lösungen entwickeln, die direkt bei den Menschen ankommen, für die wir da sind. Bereit, die Wunder der Wissenschaft zu jagen und Leben zu verbessern? Dann lass uns gemeinsam Großes bewegen – und das Außergewöhnliche entdecken.

Bei Sanofi stehen allen die gleichen Chancen offen – unabhängig von Herkunft, Hautfarbe, Religion, Geschlecht, Nationalität, sexueller Orientierung, Alter, Staatsangehörigkeit, Familienstand, Behinderung, Geschlechtsidentität, Veteranenstatus oder anderen gesetzlich geschützten Merkmalen.