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Manufacturing and Supply

Manufacturing and Supply
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M&S- IFB -Logistics Lead IFB Project

Beijing, China
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Our teams produce and deliver over 4 billion units of medicines and vaccines every year, ensuring every breakthrough gets to the people who need it most.
Our state-of-the-art facilities, AI-powered smart factories, and cutting-edge automation are redefining what’s possible: ensuring treatments reach patients faster, safer, and more sustainably than ever before. This is where your skills, ambition, and passion can shape the future of healthcare.

Background

Sanofi has decided to invest in new, state-of-the-art production facilities for insulin API 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 for insulin API.

Position Overview

We are looking for a Logistics Lead who will be responsible for ensuring the smooth and efficient import/export operations and customs clearance for all materials and equipment required for the IFB project. This includes raw materials, single-use materials, consumables, and especially machinery/equipment delivered from around the world during the project phase.

This position plays a crucial role in supporting the construction, start-up phase, and routine operation of our new state-of-the-art insulin production facility in Beijing, with a primary focus on customs compliance and trade facilitation.

The successful candidate will work in close partnership with Engineering, Operations, Quality, Supply Chain/Procurement teams, and external customs authorities to ensure seamless logistics operations.

Responsibilities

  • Lead all import/export compliance activities for the IFB project, ensuring adherence to Chinese customs regulations and international trade requirements

  • Manage customs clearance processes for all incoming shipments including raw materials, single-use materials, consumables, and equipment from global suppliers

  • Serve as the primary point of contact with custom related IFB topics and represent the IFB project during customs inspections and AEO (Authorized Economic Operator) audits

  • Complete mandatory onboarding training with certification before executing any import/export related activities

  • Act as key user of the Beijing pharmaceutical import/export community, owning all logistics activities for the IFB project

  • Manage shared logistics accounts (e.g., DHL) and serve as the owner for trade & customs compliance matters

  • Respond to all customs Q&A sessions and handle inquiries related to the IFB project during AEO inspections

  • Develop and maintain customs documentation, procedures, and Standard Operating Procedures (SOPs) in compliance with Chinese regulations

  • Coordinate with international suppliers to ensure proper documentation, labelling, and packaging for customs clearance

  • Monitor and optimize customs processes to minimize delays and ensure timely delivery of critical materials and equipment

  • Identify and mitigate customs-related risks; develop contingency plans for potential delays or compliance issues

  • Maintain accurate records of all import/export activities and ensure proper documentation for regulatory compliance

  • Collaborate with Quality Assurance to ensure imported materials meet both customs and GMP requirements

  • Support cost optimization through efficient customs procedures and duty management

  • Participate in cross-functional project meetings and represent logistics/customs interests

About You

Experience

  • Bachelor's or Master's degree in Logistics, International Trade, Supply Chain Management, Business Administration, or a related field

  • Alternatively, equivalent qualification with extensive experience in customs/import-export operations within pharmaceutical or regulated industries

  • More than 5 years of professional experience in logistics, customs clearance, or international trade, preferably in a pharmaceutical or GMP-regulated environment

  • Proven expertise in Chinese customs regulations, import/export procedures, and AEO requirements

  • Experience with customs documentation, tariff classifications, and duty management

  • Knowledge of international shipping terms (Incoterms) and trade compliance

  • Experience with ERP systems and customs management software

Skills

  • Fluent in Chinese (Mandarin) and English – both written and spoken (required)

  • Strong knowledge of Chinese customs laws, regulations, and procedures

  • Experience with AEO (Authorized Economic Operator) requirements and customs audits

  • Understanding of GMP guidelines and their application to material imports

  • Excellent organizational and planning skills with attention to detail

  • 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

  • Excellent communication and negotiation skills for dealing with customs authorities

  • Ability to collaborate closely and build cross-functional bridges with internal teams and external partners

  • Analytical mindset with problem-solving capabilities

  • Willingness to complete required import/export certification training

  • Willingness to travel to Europe for knowledge transfer and alignment with global teams

We Offer

  • An exciting opportunity to be part of a groundbreaking greenfield project

  • A dynamic, international work environment with global collaboration

  • Professional development opportunities within a leading pharmaceutical company (Top Employer of the year 2026 in China)

  • The chance to contribute to ensuring reliable insulin supply for diabetes patients worldwide

  • Comprehensive training and certification in import/export compliance

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Pursue Progress. Discover Extraordinary.

Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and 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, gender identity, protected veteran status or other characteristics protected by law.

Watch 'One day at Sanofi' and check out our Diversity Equity and Inclusion initiatives at sanofi.com

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  • Growth happens here. With bold investments in R&D and world-class facilities, Sanofians across the entire vaccine lifecycle are shaping the future of global health.

  • We do what’s right. Sustainability and DE&I drive our positive global impact—because the diverse communities Sanofians represent are the patients we serve.

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