Global Market Access Regulatory Specialist

Employment type: PARTTIME. In the role as Global Market Access Regulatory Specialist in the Market Access Team, based in the Corporate Quality department, you will contribute to our purpose of Bringing People Closer. Our core responsibility is to support and ensure world-wide Medical Device Product Registrations approvals, to be able to launch our products to the markets.

Your daily work involves cooperation with different stakeholders internally as well as externally. The team you will be part of:

You will be welcomed into a skilled team that includes 6 team members and 1 student worker at our headquarters in Ballerup, Denmark, we also have 1 team member in Kazakhstan and 3 team members in China. We have a great team culture of supporting each other whenever needed. In the team everyone has specific areas of responsibilities, with possibilities for development.

It is very important for our team to also have fun in our daily work. Your contribution is appreciated, and you will be:

Responsible for product registration cases world-wide for Medical Devices class I and IIa Responsible for submission of technical file documentation for tenders and re-imbursement appr1 …