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The Logistics / Supply Chain Associate International plays a critical role in supporting Cabaletta’s global "vein-to-vein" supply chain operations, with a strong focus on international logistics execution, trade compliance support, and vendor coordination. This role acts as the operational extension of the International Supply Chain function, ensuring seamless execution of cross-border patient material movements, close coordination with logistics providers, and alignment of supply chain processes with evolving clinical and regulatory requirements. The position is ideally suited for someone who combines strong executional rigor with an interest in developing expertise in advanced therapy supply chains and international trade.
Job Responsibility
Coordinate and oversee end-to-end international shipments (apheresis, drug product, intermediates)
Ensure full compliance with chain-of-identity (COI) and chain-of-custody (COC) requirements
Prepare, review, and validate shipping and customs documentation (commercial invoices, HS codes, import/export documentation)
Act as primary operational point of contact for couriers, customs brokers, clinical sites, and manufacturing partners
Monitor shipment status in real time and proactively manage risks, delays, and contingencies
Support implementation and execution of international trade compliance processes
Assist with HS code classification, country of origin determination, and Incoterm selection
Support Importer/Exporter of Record (IOR/EOR) processes and documentation requirements
Ensure audit-ready documentation and support inspections as required
Identify and escalate potential compliance risks or deviations
Coordinate operational interactions with logistics providers, CDMOs, and cryopreservation partners
Track and report vendor performance (e.g. on-time delivery, deviations, responsiveness)
Support issue resolution and escalation management
Assist in onboarding and qualification of new logistics vendors
Support treatment center readiness by ensuring shipping lanes and documentation processes are in place
Coordinate scheduling of patient-related shipments across stakeholders
Ensure supply chain execution aligns with clinical timelines and patient needs
Maintain accurate and audit-ready records for shipment documentation, inventories, and vendor interactions
Support development and continuous improvement of supply chain tools and tracking systems (e.g. ERP, visibility platforms)
Analyze logistics data to identify trends, risks, and improvement opportunities
Support investigation of shipment deviations, temperature excursions, and documentation discrepancies
Document and track CAPAs in collaboration with Quality teams
Identify recurring issues and support implementation of mitigation plans
Requirements
Bachelor's degree in Supply Chain, Business, Life Sciences, or a related field
equivalent or relevant higher education will also be considered
3–6 years of experience in logistics or supply chain within the pharmaceutical or biotechnology industry
Experience managing international shipments and related documentation
Strong organizational skills with high attention to detail
Excellent communication skills across internal and external stakeholders
Conversational proficiency in English and at least one additional EU language (e.g. German, French, Italian, or Spanish)
Nice to have
Experience in cell and gene therapy or advanced therapy supply chains
Exposure to cryogenic (LN2 / ultra-low temperature) logistics