The Company
Our client is a leading pharmaceutical company known for its innovative approach to medicine development. With a mission to treat, cure, and prevent diseases, they aim to make a difference for patients and society.

The Role
As a Supply Chain Analyst, you will play a key role in implementing the new EU-Medical Device Regulation over the next year, while also managing day-to-day tasks within the materials management department at the Leiden production plant.

Responsibilities
 You will work closely with the EU MDR project team to set up and collect master data, ensure stakeholders are aligned on existing processes, and initiate ERP system settings. The role requires accuracy, a good understanding of processes, and strong stakeholder management skills. You will also engage and connect with various supply chain partners across the organization, including regulatory, global supply chain, quality, and operations of the manufacturing plant. Additionally, you will support the project in finding solutions for special EUMDR requirements, such as a procedure pack.

Requirements
To be successful in this role, you should have
-5 years of experience in international supply chain/planning  
-Background in healthcare/pharma.
-A good understanding of ERP systems, preferably JDE,
-Strong communication skills in English are also necessary, with Dutch being a plus.

Please contact me to learn more, even if this role is not directly related to you. You should still apply as the client has options to train. Or you may call me at +31206589800.