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MS Solid Production Specialist Beijing

北京, 中国 Fixed Term (Fixed Term) 发布于   Sep. 09, 2026 申请截止于   Jan. 08, 2027
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Job Information 职位信息

Job title职位名称: Solid Production Specialist

•    Location工作地点: Beijing 
•    % Remote working and % of travel expected 远程办公和出差的概率:N/A
•    Job type工作类型: Permanent长期
•    Site/Unit 区域/事业部:Beijing Site

About the job工作职责
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. Your job, as Associate Manager of Quality Assurance Operation within our M&S China-BEI Site, will be to making best class medicines with excellent strategies and tools and delivering them to our patients.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?

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。
1.    Able to complete daily work independently.
个人贡献者,能够独立熟练完成日常工作
2.    Carry out daily production work strictly according to standard operating procedure.
严格按照标准操作流程执行日常生产工作
3.    Familiar with the work flow and make timely and relevant records
熟悉工作流程,做好及时的相应记录
4.    Assitant production management team to monitor production environment, process, hygiene, facilities to make sure all production activities comply with SOP requirements,
协助生产管理人员监督生产环境、工艺、卫生、设施等,确保所有生产活动符合SOP要求。
5.    Prepar the validation protocols for production process, equipments, cleaning etc.
准备进行适当的工艺、设备、清洗等验证文件。
6.     Imprementation and monitor the actions of Change Control, CAPA for deviations or complaints related to production. 
生产中所有变更、偏差及生产相关的投诉问题纠正措施和预防措施的及时落实及监控
7.    Develop necessary SOPs and ensure the implementation and improvement. 
组织制定相关的岗位操作规程并确保执行及持继改进。
8.    Be responsible for introducing, development and improvement of GMP,HSE and lean production.
 负责在GMP、HSE、精益生产等体系方面的推广、维护和改进工作。
9.     Other tasks temporarily assigned by department  manager. 
  按时完成上级临时交办的或部门间合作的其他工作任务。

Quality  Responsibility
质量职责
1.     Report product complaints and adverse drug reactions according SOP requirements.
  根据SOP要求报告产品投诉和药物不良反应。
2.    Participate in and complete personal training on time.
  按时参加并完成个人培训。
3.    Operate in accordance with SOP standards。
  按照SOP标准要求进行操作。
4.    Fill in GMP documents and records in accordance with SOP standards.
 按照SOP要求填写GMP文件和记录。
5.    Report abnormal conditions in a timely manner.
  及时汇报异常情况。

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。
Education / Experience    
1.    Bachelor degree education or above, with major on pharmaceutical or related.    
本科及以上学历, 制药或相关专业。 

Technical skills & Competencies / Language    
1.    Proficient English communication skill (written and verbal) ,  Priority will be given to those with experience studying abroad.
良好的英语听、说、读、写能力,具有出国留学经历优先。
2.     Excellent MS office skills 
能够熟练使用办公软件

Behavioural Competencies(LEAD and others)    
1.    Excellent communication and coordination skills.                    
  卓越的沟通和组织协调能力
Be good at continuous improvement.                                      
2.     善于发现并推进持续改进


Why choose us?
•    Bring the miracles of science to life alongside a supportive, future-focused team.
•    Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
•    Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
•    Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.

Pursue Progress. Discover Extraordinary.
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. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s discover extraordinary together.

At Sanofi, we provide equal opportunities to all regardless of race, color, 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!

追寻 发展探索 菲凡

加入赛诺菲,开启科学新时代。在这里,你的成长将如我们的工作成果一样具有变革性。我们帮助你发展,助你走得更远、思考得更快、做前所未有的事。你将与我们一起突破边界、挑战常规,打造更智慧的解决方案,惠及全球社区。准备好追寻科学的奇迹,改善人们的生活了吗?让我们携手追寻发展,探索非凡。

赛诺菲致力于为所有员工提供平等的就业机会,不因种族、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、性别认同、受保护的退伍军人身份或其他受法律保护的特征而有所差异。

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