Global Trade
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Position Overview
The Manager, Global Trade & Customs Optimization is an individual contributor responsible for driving compliant duty optimization and classification governance across Integra LifeSciences’ global supply chain, with primary focus on transatlantic (US–EU) and EMEA trade flows.
Key responsibilities include:
- Global HS Classification Governance – lead and maintain global HS classification for finished products, components, and spare parts; analyze engineering documentation, technical specifications, and BOMs; maintain alignment across key jurisdictions; support Binding Tariff Information and US binding ruling submissions; conduct classification reviews.
- Transatlantic Duty & Tariff Optimization – identify tariff engineering opportunities within US–EU supply flows; assess duty impact; support FTA utilization (USMCA where relevant, EU FTAs, UK TCA); contribute to landed cost analysis and scenario modeling; partner with Logistics CoE on customs procedure optimization.
- Origin & Supply Chain Support – support origin determination and supplier declaration governance; partner with Procurement and Supply Chain to improve origin data quality; provide trade impact analysis during new product introductions and site changes; monitor global tariff and geopolitical developments affecting US–EU flows.
- Compliance & Risk Management – ensure all optimization initiatives align with global customs laws and internal compliance standards; maintain audit‑ready classification and origin documentation; support customs audits and broker oversight; drive continuous improvement of trade‑related processes within the Logistics CoE.
Qualifications
- Bachelor’s degree in International Trade, Supply Chain, Business, Engineering, or related field.
- 5–8 years of experience in global trade compliance or customs.
- Strong hands‑on experience with HS classification (EU CN/TARIC and/or US HTS).
- Working knowledge of origin rules and FTAs impacting US–EU trade.
- Experience supporting duty savings or tariff mitigation initiatives.
- Ability to interpret technical product documentation.
- Strong analytical and stakeholder management skills.
- Fluent in English.
- Preferred: Experience in medical device, life sciences, or regulated manufacturing; experience supporting US import flows or working with US customs brokers; familiarity with SAP or Global Trade Management systems; customs broker license or equivalent certification.
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