Are you the Regulatory Consultant - Medical Devices we're looking for?

You:

  • have an MSc/PhD in Pharmacy, Chemistry, Medical Biology, Life Sciences
  • will prepare and update technical documentation (eg. STED, BSER, CER, RMP) 
  • will coordinate and manage interactions with notified bodies
  • prepare and maintain ISO 13485 quality management systems
  • act as authorised representative

We:

  • will coach you and provide training, if needed
  • invite you to apply by This email address is being protected from spambots. You need JavaScript enabled to view it. your CV and motivation.

Check out the detailed description!

Zwiers Regulatory Consultancy | Pivot Park | Henry Chesbrough building | Kloosterstraat 9 | 5349 AB Oss | The Netherlands
Zwiers Regulatory Consultancy | Matrix V |Science park 406 | 1098 XH Amsterdam | The Netherlands

Tel +31 (0)6 10489150 | info@az-regulatory.com