Full time - permanent role
Within the medical devices industry I am looking for an RA Specialist who can support the new MDR.
In your role as RA Specialist you will be responsible for all Regulatory Affairs and Quality Assurance (20%) in the European region as well as being responsible for the MDR implementation. Providing training on new or changed regulations and processes. You'll receive messages from all over the globe especially from the EMEA region. You will also be supporting European sales support on Regulatory Affairs.
What we offer
-Salary 57K - 67K
-Laptop / IPhone
What you have
-Minimum bachelor within Life Sciences preferred Engineering
-Minimum of five year's experience within Regulatory Affairs / Quality Assurance
-Familiar with MDR
-You can lead a project (MDR)
Are you ready for the next step in your carrier and are you interested in this position? Feel free to contact me: Iris Rettob Recruitment Consultant +31 20 - 522 15 77 |