Import/Export Compliance Specialist

Posted 12 Hours Ago
Be an Early Applicant
Gent, BEL
In-Office
Mid level
Healthtech • Manufacturing
The Role
Validate and maintain tariff and country-of-origin data, perform restricted party screening and ECCN classifications, support daily import/export operations and customs clearance, monitor regulatory changes, coordinate with cross-functional teams and external brokers, and support audits and continuous improvement of trade compliance processes.
Summary Generated by Built In

Changing lives. Building Careers.
Joining us is a chance for you to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, more than 4,000 of us are challenging what’s possible and making headway to help improve outcomes.

The Import/Export Compliance Specialist is responsible for validating and maintaining Tariff Codes and Country of Origin validation, assisting, and supporting the Trade Compliance team and Manager to ensure compliance with all EU Customs and other Government Agency requirements and regulations relating to import; as well as EU export requirements and regulations, trade sanctioned country management**, export control compliance, denied/restricted party screening,** and other trade compliance matters related to acquisition project(s). This person will assist our global offices as needed. This person will be working to improve compliance and assist with implementing best business practices related to customs, export controls, and international trade operations.

RESPONSIBILITIES

  • Monitor Global Trade Management (GTM) system transactions on hold and take necessary action
  • Assign, validate, and maintain customs tariff classifications (HS / CN / TARIC), ECCN classifications and Country of Origin data for globally traded products
  • Perform Restricted Party Screening (RPSL/DPL) and support export control and sanctions compliance activities, including due diligence reviews and escalations
  • Support daily import/export operations, including review of shipping and customs documentation, customs clearance support, and coordination with customs brokers and freight forwarders
  • Assist with Free Trade Agreement (FTA) validations, End User Agreements, and other import/export compliance documentation requirements
  • Support maintenance and continuous improvement of trade compliance programs, procedures, ERP/GTM data, and internal controls
  • Monitor regulatory changes impacting import/export activities and support implementation of required business process updates
  • Investigate and follow up on shipment delays, customs issues, and documentation discrepancies
  • Partner with cross-functional teams including Customer Care, Distribution, Procurement, Service & Repair, Tax & Finance, QA/Regulatory, and Transportation to support trade compliance requirements
  • Support audits, compliance reviews, and other Trade Compliance projects as assigned
  • Minimal travel may be required to meet business needs (estimated 10%)

QUALIFICATIONS

  • Minimum of three (3) years of experience in Import/Export Customs Compliance, with practical knowledge of international trade, customs, and export regulations
  • Proficiency with customs tariff classifications (HS / CN / TARIC), ECCN classifications, and Country of Origin validation
  • Proficiency with EU Dual-Use Regulation, export controls, and sanctions compliance requirements
  • Working knowledge of Enterprise Resource Planning (ERP) systems, Oracle preferred, and Global Trade Management (GTM) systems
  • Working understanding of Restricted Party Screening tools, such as Descartes, Kharon, or Securimate preferred
  • Experience supporting daily import/export operations, customs clearance activities, and shipping/customs documentation review preferred
  • Excellent verbal and written communication skills with proficiency in English
  • Proficiency in MS Excel, Word, and PowerPoint
  • Strongly preferred but not required: experience in a multinational manufacturing and distribution company, especially within the medical device or pharmaceutical industry

Unsolicited Agency Submission

Integra LifeSciences does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. A formal written agreement is required before engaging any agency, and it must be executed and authorized by the Vice President, Talent Acquisition. Where agency agreements are in place, introductions (the initial sharing of a candidate’s name, resume, or background) are position-specific and may only occur within the scope of that approved agreement. Please, no phone calls or emails.

Skills Required

  • Minimum of three (3) years of experience in Import/Export Customs Compliance
  • Proficiency with customs tariff classifications (HS / CN / TARIC)
  • Proficiency with ECCN classifications and Country of Origin validation
  • Proficiency with EU Dual-Use Regulation, export controls, and sanctions compliance requirements
  • Working knowledge of Enterprise Resource Planning (ERP) systems
  • Working knowledge of Global Trade Management (GTM) systems
  • Working knowledge of Oracle (preferred)
  • Working understanding of Restricted Party Screening tools (e.g., Descartes, Kharon, Securimate)
  • Experience supporting daily import/export operations, customs clearance, and shipping/customs documentation review
  • Excellent verbal and written communication skills with proficiency in English
  • Proficiency in Microsoft Excel, Word, and PowerPoint
  • Experience in a multinational manufacturing and distribution company, especially medical device or pharmaceutical industry
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The Company
HQ: Princeton, New Jersey
3,489 Employees

What We Do

Integra LifeSciences, a world leader in medical technology with headquarters in Princeton, New Jersey, was founded in 1989 with the acquisition of an engineered collagen technology platform used to repair and regenerate tissue. Since then, Integra has expanded its base regenerative technology product portfolio to include surgical instruments, neurosurgical products and advanced wound care products, through global acquisitions and development of new and innovative products and technologies to address unmet patient needs and improve outcomes. Integra is a global leader in neurosurgery and offers a broad portfolio of products and solutions for dural access and repair, cerebral spinal fluid management and neuro-critical care. Our regenerative tissue technologies include products that address soft tissue, nerve and tendon repairs and for the treatment of acute and chronic wounds, burns, as well as for plastic and reconstructive surgery. The company has offices, manufacturing and research facilities in Asia, Australia, Europe, Middle East, and the Americas. Integra products are ubiquitous in many hospital intensive care units and operating rooms around the world. Some of our high quality leading brands include AmnioExcel®, Bactiseal®, CerebroFlo®, CereLink® Certas® Plus, Codman®, CUSA®, Cytal®, DuraGen®, DuraSeal®, Gentrix®, ICP Express®, Integra®, MatriStem® UBM, MAYFIELD®, MediHoney®, MicroFrance®, MicroMatrix®, NeuraGen®, NeuraGen® 3D, PriMatrix®, SurgiMend®, TCC-EZ® and VersaTru® and are available through a combination of directly employed sales representatives, distributors and wholesalers

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