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USP Engineer 上游工程师

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Onsite

USP Engineer 上游工程师

山东赛诺菲电子科技有限公司

USP Engineer 上游工程师

2 months ago

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Important information


Contract type:

Permanent

Location:

Beijing, China

Work mode:

Onsite

Published on:

24 August 2026

What they need


该职位来源于猎聘 招聘:上游工艺专家 1位 注意:所示薪资为预算参考值,实际offer将基于候选人资质和当前薪资灵活调整,可能高于或低于标注范围。

  • USP Engineer: Upstream / Fermentation
  • MSP Engineer: Midstream / cell harvest
  • DSP Engineer: Downstream I / High Purification, Chromatography
  • DSP Engineer: Downstream II / Isolation and Drying 必须要求:原液生产背景、英语口语技能(与海外沟通) Background Sanofi has decided to invest in new, state-of-the-art production facilities for the entire insulin portfolio as part of the InsuLINK program, to ensure a future-oriented, sustainable, and reliable long-term supply for diabetes patients worldwide. Beijing, China (IFB = Insulin Facility Beijing) and Frankfurt, Germany (IFF = Insulin Facility Frankfurt) have been selected as the locations for the two facilities. The new production facilities will be designed as fully automated, environmentally friendly, and state-of-the-art biologics facilities that consider the specific process requirements of all insulins. Position Overview They will report to the respective department heads of USP, MSP, DSP I and DSP II. These positions play a crucial role in the design, planning, construction, and commissioning of our new state-of-the-art insulin production facility in Beijing, as well as the product transfer into routine production. The successful candidates will work within the Operations unit in close partnership with the Engineering teams to help shape the success of this project. Responsibilities
  • Represents the know-how and operational knowledge of their workstreams within the project team
  • Supports the project tasks of their teams in various phases of the engineering/construction project, e.g., planning and design, P&ID review, HAZOP, functional design
  • Partnership and collaboration with Engineering on various project topics: Creation of process-relevant user requirements Equipment and system designs Development of Standard Operating Procedures (SOPs) and operational documentation Commissioning of equipment and systems
  • Partner in OQ/PQ/PPQ execution for the manufacture of insulin
  • Partnership with MSAT in technology transfer and scale-up activities, efficient collaboration in highly cross-functional teams About You
  • Experience Bachelor’s degree in chemical engineering, Biotechnology, Bio-engineering, or a related field Alternatively, qualification as a Technician/Master Craftsman with many years of experience in a production environment in pharmaceutical manufacturing More than 2 years of industrial experience in the pharmaceutical environment with a strong focus on the manufacture of insulins, biologics or other pharmaceutical substances cGMP knowledge Technical background in insulin manufacturing is a plus
  • Skills Ability to work under high pressure in a constantly changing project environment Ability to work in a highly matrix-driven project environment with strong functional reporting lines Leadership skills for both functional and directly reporting teams Excellent teamwork and communication skills Ability to collaborate closely and build cross-functional bridges Willingness to travel to Germany for knowledge transfer Basic English language skills

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