Associate Clinical Supply Chain Breda • SIRE Life Sciences
Gevraagd
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37 - 40 uur
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Engels (taal)
Aanbod
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Vast contract
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About the company
This global biotechnology company develops and delivers innovative therapies to address serious illnesses. Their site in the Breda plays a critical role in ensuring global clinical trials are supported with the right medication at the right time. Within their Clinical Supply Chain team, every detail, from label artwork to master data setup, directly impacts the success of global studies.
Role description
As an Associate Clinical Supply Chain, you’ll be part of the team responsible for designing and setting up the global clinical supply chains that support patient trials worldwide. This role ensures the correct system setup, documentation, and coordination of key supply chain components that enable timely trial starts. You’ll work closely with Clinical Supply Project Managers and cross-functional partners in a GMP and GxP regulated environment.
Key responsibilities
- Support the creation and maintenance of master data in SAP (including materials, BOMs, WBS elements)
- Initiate and track label artwork creation and follow up on open issues
- Prepare and update Product Specification Files (PSFs) for each study
- Set up Study Design Tables and cross-dock/depot plans to support global logistics
- Maintain metrics and contribute to workforce planning reports
- Act as the point of contact for SAP readiness activities
- Bachelor’s degree in Logistics, Life Sciences, or Business Administration
- Familiarity with supply chain principles and planning
- Experience in clinical supply chain or regulated environments
- Understanding of GxP, ICH guidelines, or Clinical Trial Directives
- Experience with SAP
- Strong experience with MS Office (especially Excel and Word)
- Fluent in English, both spoken and written
- High attention to detail and accuracy
- Able to prioritize, work in a structured way, and escalate when needed
55493
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