- Dutch and English speaking - MUST
- Located in EU
- Graduate of the Engineering, Pharmaceutical, Chemistry or Biological Sciences;
- Communication skills (oral-written);
- Work experience (1-3 years) in the regulatory area of device, local regulations (MDD/MDR/MEDDEV) , interactions with MEB/CIBG, MHRA
- Regulatory documentation: FSC, GMPs, ISO, legalization, apostilles, etc.;
- Development of databases, pivot tables, macros in Excel, Access.
- Country notification, class I registration into dutch CA database
- Free sale certificates support worldwide – CIBG management interaction
- MHRA/Eudamed databases support
- MDR readiness for authorized representative- SOP development
Start Date: ASAP
To find out more or call me on +31 2020 44 502!
Shoot your CV in my inbox ASAP as this role will be filled by end of next week