Freelance RAQA specialist

Location: Noord-Holland - Netherlands

Job: Medical Device - Contract

For a medical device company in North-Holland I am currently looking for an RAQA specialist. They are looking for someone to create regulatory strategies for new products, manage filing activities and providing regulatory expertise.


  • You will be managing the product registration activities, Filing, technical files and International registrations
  • You will be preparing annual licensing renewals and product registration
  • You will be reviewing and approving product labeling and promotional materials
  • You will be reviewing and approving document change orders
  • You will be assisting the product safety team 
  • You will  be providing input on the Medical Device Vigilance activities


  • Degree in Life scienes
  • At least 3 years related experience with Medical device or pharmaceutical industry
  • Understanding of the QMS regulations (ISO 13485 and the new MDR)
  • Flueancy in English 

Project Duration:

6 months

Start date:



If you’re interested in the above description, please apply with your CV and a letter of motivation by clicking on the ‘apply’ button below.

For further information, please contact Loretta Kumi at +31 (0)20 20 44 502 or by email at


Reference: vr5492


If you see yourself in this role, please apply by uploading your CV via the apply for this position button. We will review your application and get in touch with you to discuss things further.

For more information, please fill in the form below or call us on +31 (0)20 20 44 502.

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