Company

Our client is an international organization, setting up European Head Quarters in Rotterdam area. They manufacture and distribute high quality sport articles on a global scale for indoor sports.

Your main focus and responsibility is to analyze the impacts of the new European Medical Device Regulation and to coordinate this with the various Supply Chain Planning teams. You’ll work with our global design sites to understand the recertification program (products and timing). Based on this plan, you’ll work with the demand, inventory, and supply planning teams to implement the requirements for safety stock requirements and stock segregation.

General Funtions

• You coordinate the recertification plan with our 24 global design sites;

• You review the status of the recertification plan with the design sites;

• You review required stock coverage based on information from Regulatory on International registration and risk mitigation;

• You coordinate planning adjustments with demand planning, inventory planning, and supply planning;

• You coordinate implementation of stock segregation and distribution controls;

• You review and update data in the MDR Product Master Data tool;

• You update KPI and prepare reports for the ‘Sales and Operations Planning’ meetings and MDR review meetings.

The companies team members share the singular purpose of working to restore mobility and improve the quality of life for patients around the world. They are looking for team members who would like to make a difference in people's lives. They are always searching for talented, dedicated and motivated people with a range of skills, experiences and backgrounds to join their team. Are you next to join them?

• You have a Bachelor degree in Logistics, Supply Chain or Operations Management or equivalent working and thinking level;

• You have a minimum of 4 year relevant working experience in Supply Chain and/or Operations with prove Project Management experience;

• You have excellent knowledge of ERP systems (SAP MM & PP), support tools (Every Angle, SAP BW) as well as MS applications (Excel/Access);

• You are an effective communicator and know how to work together with different teams;

• If you have a certification in APICS CPIM, CSCP AND/OR Lean Six Sigma Green/Black Belt it’s a plus;

• It’s a strong plus when you have an understanding of Medical Device Regulations;

• You are fluent in English (written and verbal) and it’s a plus when you speak Dutch.

   

What they offer

This is your chance to push the boundaries of innovation and make a valued contribution to helping people around the world find renewed vitality starts here!

They offer you a responsible job in an exciting, dynamic and growing environment, to make it even better they also:

• support you with thorough training and continuous development;

• offer an attractive compensation package;

• make sure you will get to chance to travel to their other locations (but this won’t take up to much of your time);

• this challenging project will take up the next two years. After that, they will see together if there is a new challenge within the company for you.

How to Apply

If you are interested and you meet all the above requirements send your resume with a motivation letter via this website or call Monique Nobel +31 (0) 6 41 576 904.