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Location
In office (Beijing)
Seniority
Staff · 10+ years exp
Employment
Full-Time
Overview
Company
Impact
Profile match
Sanofi is a French pharmaceutical company formed in 1973 and assembled over five decades through a long series of mergers including Synthelabo, Aventis and Genzyme. It is now built around immunology and rare disease, with Dupixent for atopic dermatitis and asthma as by far its largest product, alongside a substantial vaccines division covering influenza, meningitis and the respiratory syncytial virus antibody Beyfortus. Headquartered in Paris, the group has sharpened its focus in recent years by separating its consumer healthcare business into the standalone company Opella and directing research spending toward biologics and immune science.

About the job

Sanofi has decided to invest into a new large state-of-the art facility for Insulin Drug Substance in Beijing, China. For this green field operation, we’re enhancing our legacy of excellence and build on decades of expertise on the whole value chain of insulin manufacturing. The new facility will be designed as a fully automated, green, modern, and state-of-the-art biologics facility. A large global and highly cross-functional program organization will be established to lead and execute the program until commercial routine manufacturing.

Meet Katrin, our Global Program Leader, and discover how we’re transforming insulin production. Watch now!

Main responsibilities

Please indicate here the main job responsibilities

During Project stage

  • Collaborate strongly with IFF Program teams to Manage all insulin downstream process systems (DSP) maintenance activities (e.g., chromatography, crystallization, drying) from Basic Engineering to Detailed Design studies with optimized solutions leveraging Frankfurt process replication while integrating China local rules & codes
  • Collaborate to URS, maintainability reviews (P&IDs, Layout, 3D model, Flows…), FMECA sessions for DSP within IFB project ensuring later installation, commissioning, and operation of DSP equipment in line with reliability, accessibility, detachability, detectability, operability of energy control device, integrity of protective device, availability of hazardous substances control, and resource expectations
  • participate in and provide technical support for FAT, commissioning, SAT, qualification activities and start-up on DSP
  • Participate in HAZID/HAZOP analysis with process risk team to help improve Design.
  • Drive the design, specification, and implementation of maintenance activities for DSP operations, ensuring compliance with GMP and Sanofi standards
  • Act as the primary interface for DSP with internal work teams such as Process, Automation, CQV, CSV, and Digital, as well as with external vendors and engineering partners

During operation stage

  • Oversee the daily maintenance, preventive maintenance (PM), troubleshooting, and emergency repair of equipment in insulin DSP, ensuring seamless data flow and operational performance across the manufacturing floor. This role ensures the stable, efficient, and compliant operation of DSP to meet production schedules, quality standards (GMP), and regulatory requirements (FDA/EMA)
  • Involved in Greenfield Integration, including specific equipment related with CUB/ Warehouse/ WWTP
  • Strictly comply with maintenance/calibrationSOPs and EHS regulations, be proficient in LOTO and other safety procedures
  • Develop and maintain clear documentation, functional specifications, and testing protocols for DSP
  • Initiate and maintain technical communications with equipment suppliers, while systematically tracking all after-sales service activities
  • Oversee spare parts inventory status, maintaining precise stock records and initiating procurement based on annual maintenance plans and equipment failure analysis to minimize MTTR
  • Work in close coordination with multiple departments including EHS, PD, QA, QC and others to achieve operational excellence
  • Regularly engaged in technical problem-solving discussions in English with IFF maintenance teams

About you

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

  • More than 10 years of PD equipment maintenance experience in the pharmaceutical industry (preferred), or in GMP-regulated industries such as biotechnology/fine chemicals/food and beverage
  • Familiarity with mechanical structure, working principles of PD equipment and experience in maintain
  • Familiarity with GMP standards/compliance, including data integrity requirements, change control, deviation handling, preventive maintenance, and calibration
  • Proficiency in writing and reviewing GMP documents such as maintenance work orders, preventive maintenance plans, spare parts inventory management, deviation reports, and change control
  • Proficient in common office software and maintenance software

Soft and technical skills:

  • Good communication (internal and external), teamwork, problem-solving skills

Education:

  • bachelor’s degree in industrial engineering domain: Mechanical/Electric engineering/ Automation/ Mechatronics/Pharmaceuticalengineering

Languages:

  • Chinese , Engineering English

Pursue progress, discover extraordinary

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, ability or gender identity.

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

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