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BeOne

Global oncology therapeutics discovery, development, manufacturing

Associate Director - Global Commercial Trade Compliance

Regulatory Compliance & Ethics +1Confirmed live in the last 24 hours
Full-timeRemote in USA

About the Job

Requirements

  • A Bachelor's degree in Business Administration, Operations Management, or a similar field and at least 8 years of progressive experience in Global Trade Compliance are required.
  • A Master's degree and at least 6 years of progressive experience in Trade Compliance are required; experience within the biotech, pharmaceutical, or CRO industry is preferred.
  • Five or more years of managerial experience directly managing people, or leadership experience leading teams, projects, or programs or directing resource allocation, is preferred.
  • Proficiency in Microsoft Word, Excel, and Outlook is required.
  • Advanced expertise in global trade management systems, transportation management system architecture, and enterprise resource planning platforms such as SAP is required.
  • Early morning or evening meetings may be required due to the company's global operations.

Responsibilities

  • Provide enterprise-wide strategic leadership for global trade compliance and operations, including designing, implementing, and overseeing international import and export compliance programs.
  • Direct corporate multi-jurisdictional customs governance and compliance with U.S. Customs and Border Protection and parallel international customs authorities across EMEA, APAC, and Latin America.
  • Standardize and audit worldwide trade master data, ensuring accurate Harmonized Tariff Schedule classifications, country of origin data, and structural customs valuation methodologies.
  • Design and execute corporate programs to capture duty savings through Free Trade Agreements, Duty Drawback, bonded warehouses, and Foreign Trade Zones.
  • Direct the cross-border compliance framework for commercial drug products and biologics; ensure FDA master data is accurate and used throughout the supply chain and in equivalent international processes; serve as lead investigator and responder for FDA import alerts.
  • Govern the import and export of animal-derived components, biological media, cell lines, and enzymes used in biopharmaceutical manufacturing; coordinate with the Animal and Plant Health Inspection Service to secure import permits and veterinary health certificates and equivalent international authorizations.
  • Direct trade compliance programs for chemical formulations and laboratory reagents under the Toxic Substances Control Act; manage positive and negative TSCA certifications and equivalent international requirements.
  • Direct licensing and declarations for pharmaceutical ingredients, active elements, or research materials derived from protected animal or plant species under CITES and the Endangered Species Act, including equivalent international requirements.
  • Maintain strategy and processes for internal trade assessments, external government audits, and submissions of PSCs and PDs.
  • Maintain global service-level agreements, standard operating procedures, and key performance indicators for international customs brokers and freight forwarders to minimize clearance delays.
  • Develop global trusted trader programs, including C-TPAT, AEO, and PIP.
  • Work within a cross-functional team to improve deemed-export, export-control and sanctions-screening, and dual-use programs.

Desired Qualifications

  • Trade Compliance experience within the biotech, pharmaceutical, or CRO industry.
  • Five or more years of managerial experience directly managing people, or leadership experience leading teams, projects, or programs or directing resource allocation.

About the Company

BeOne

Global oncology therapeutics discovery, development, manufacturing

BeOne Medicines discovers, develops, and commercializes oncology therapies worldwide, focusing on hematologic cancers and solid tumors. Its products work by leveraging internal R&D and clinical development to bring therapies to market quickly, with Brukinsa serving as a leading backbone in the US and European markets. It differentiates itself through a large-scale global clinical network and cost-efficient development and manufacturing that support high margins and a focus on large-market cancer indications. Its goal is to expand access to high-impact, affordable cancer treatments across more than 45 countries while growing its pipeline into immunology and solid tumors.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Dongcheng District, China
Founded
2010

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