As part of the Development Supply Chain team, you will be responsible to ensure efficient and compliant distribution of investigation products on a global scale.
Besides that, you need to ensure timely and compliant shipping of investigational products to clinical sites and LSPs. you ensure a timely resolution of shipping issues and tier 1 questions.
You will also ensure timely and accurate processing of temperature data reviews and temperature excursions and take care of accurate management of assigned SME area(s) and KPIs, and you will also provide training and maintain a knowledge base on assigned SME areas.
In this vital role, you will:
- Control the Sales Order management and the Stock Transfer order management;
- Handle manual and electronic Proof of Receipt and the Temperature data review;
- Own the site and transit temperature excursions and the returns and reconciliations;
- Support expiry relabeling campaigns and the Import license management;
- Be responsible for one or more subject matter expert areas.
- Handling and processing of distribution complaints.
What we expect of you
- Bachelor’s degree in Clinical Supply Chain or similar;
- Previous experience in Clinical Supply Chain Management, preferably in the biotechnology or pharmaceutical industry;
- Proficiency in English, both in an oral and written communication;
- Advanced understanding of regulatory guidelines impacting clinical supplies;
- Good knowledge of Enterprise Resource Planning systems;
- Demonstrated experience in working with automated systems (computer-based business systems) like MS-Office.
Interested? Send your CV to Daria at d.finikova@panda-int.com or call +31202044502 for more info.