RA Specialst

Location Heerlen
Discipline: Medical Device
Job type: Temporary/Freelance
Contact name: Caitlin Girdwood

Contact email: c.girdwood@panda-int.com
Job ref: 11597
Published: about 1 month ago
Working closely with renowned Medtech company in the Netherlands who are looking for RA Consultants to assist their 2021 projects:

Key skills:

  • 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.

Key tasks:

  • 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