Logistiek manager

• Manage and maintain master data in SAP (materials, BOMs, WBS elements, custom values, study design tables).
• Coordinate the creation and approval of clinical artwork and related documentation.
• Create and maintain Product Specification Files throughout the clinical trial lifecycle.
• Support third-party depot setup and cross-dock planning.
• Monitor metrics and contribute to workforce planning cycles.
• Ensure adherence to GMP/GDP/GDocP and regulatory guidelines.

Requirements

• Bachelor's degree in Supply Chain, Business Administration, Life Sciences or a related field.
• Relevant experience in an international and regulated environment, preferably within biotechnology or pharmaceuticals.
• Solid understanding of supply chain principles (especially BOM).
• Experience with planning and project coordination.
• Strong Excel and MS Office skills; SAP experience is a plus.
• Fluency in English, both spoken and written.
• High attention to detail, ability to prioritise and escalate issues when needed.

• Knowledge of clinical supply chain management processes.
• Familiarity with GxP and ICH guidelines.
• Excellent communication and problem-solving skills.

Benefits

• A challenging temporary assignment (contract via Undutchables).
• Start date: latest 1 December 2025.
• Hybrid role: onsite presence expected during the first 3–5 months.
• A dynamic, international, and collaborative work environment in a leading biotech organisation.
• Competitive compensation in line with market standards.

Application Procedure