Import-Export Compliance Expert, Biotech

About Gen Script

GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript’s businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.

GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.

Pro Bio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy (CGT), vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. Pro Bio’s total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing.

In terms of plasmid service, Pro Bio supports the most clinical approvals for CGT drugs including mRNA vaccines, CAR‑T in China. It is also the first GMP manufacturing platform to provide in vitro transcription (IVT) template linearized plasmids for mRNA vaccines and has supported several mRNA vaccine global enterprises to obtain clinical approvals. In terms of viral vector service, Pro Bio has a stable and high‑yield viral vector platform.

GenScript Europe division, headquartered in Rijswijk, Netherlands, with a branch office in Oxford, UK, was established in 2019 to serve as a hub for commercial, technical support and logistic in the European and UK region. In our ongoing commitment to enhancing service for our EU clients, we are planning to build our first laboratory facility in the Netherlands in the coming year.

Location:

Rijswijk, the Netherlands

Working Scheme:
Hybrid

Working Hours:

40 hours per week

• Import & Export Compliance Program Management:
  • Develop, implement, and oversee the company’s import & export control compliance program, ensuring adherence to EU, UK and global regulations.
  • Create and maintain import & export control policies, procedures, facilitating compliance across all levels and multi‑country requirements.
  • Address global trade compliance requirements, including imports and exports involving production sites worldwide (CN, SG, US, EU).
• Import & Export Operations Support:
  • Oversee the preparation, submission, and review of import and export documentation, ensuring accuracy and compliance with EU and UK authority requirements.
  • Maintain meticulous record-keeping practices for audit and regulatory review purposes.
  • Conduct both EU and UK HS code classification based on product information and issuing Customs commodity description based on the customs elements. Capable of managing classification via Integration Point and sub system for daily classification operations.
  • Ability to explain the HS classification principles and implications with external Customs/Brokers and internal team members and global counterpart to facilitate the HS code accuracy globally.
• Regulatory Monitoring and Reporting:
  • Stay informed about updates to EU and UK import & export control regulations and communicate their impact to relevant internal stakeholders.
  • Provide timely advice on compliance measures and required adaptations to maintain operational integrity.
• Risk Assessment and Continuous Improvement:
  • Conduct regular risk assessments and internal audits to evaluate the effectiveness of the compliance program.
  • Identify areas for improvement and adapt the program to align with regulatory changes or organizational needs.
• Import & Export Licenses and Documentation Management:
  • Manage the application, renewal, and maintenance of import & export licenses, ensuring timely submission and approval.
  • Handle import & export exemptions where applicable and ensure all documentation is complete, accurate, and compliant.
• Collaboration and Stakeholder Management:
  • Work closely with…