Global Clinical Logistics Specialist — IMP Shipment Expert

Actalent; Kaiseraugst; Vor Ort; CHF 90.000 - 130.000; Vollzeit

Zusammenfassung

Actalent is seeking a Logistics Specialist (Global Clinical Distribution) for a Kaiseraugst, Switzerland-based role. This is a majority onsite, long-term contract with strong extension potential, supporting global clinical distribution networks for IMPs and related shipments.

You will manage international shipments, ensure GDP compliance, handle licenses and permits, and collaborate with warehousing, transportation, and regulatory teams across regions. Fluency in German and English is required.

Qualifikationen

• Completed degree or vocational training in Supply Chain Management, Logistics, Clinical Supply Chain, or a related field.

Aufgaben

• Manage and coordinate international clinical supply shipments, including IMPs.
• Handle shipment documentation, permits, and licenses in compliance with country-specific regulations.
• Monitor shipments proactively and resolve transportation or customs-related issues.
• Maintain and update country-specific import/export requirements.
• Serve as the primary contact for logistics and shipping-related questions from internal and external stakeholders.
• Collaborate with warehouse, transportation, customs, and supply chain teams across multiple global locations.
• Support continuous improvement initiatives and logistics projects.

Kenntnisse

GDP knowledge

IT affinity

Prioritization in fast-paced env

Ausbildung

Supply Chain Management

Logistics

Clinical Supply Chain

Related field

Tools

SAP

ERP systems

Jobbeschreibung

Actalent is seeking a Logistics Specialist (Global Clinical Distribution) for a Kaiseraugst, Switzerland-based role. This is a majority onsite, long-term contract with strong extension potential, supporting global clinical distribution networks for IMPs and related shipments.

You will manage international shipments, ensure GDP compliance, handle licenses and permits, and collaborate with warehousing, transportation, and regulatory teams across regions. Fluency in German and English is required.