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Regulatory affairs specialist

Regulatory affairs specialist

Location., Belgium
Business SectorMedical Devices
Contact nameJoshua Williams
Contact emailj.williams@panda-int.com
Job ref20373
Published26 days ago

Currently I'm exclusively collaborating with my Medtech client near Gent , who are in need of an RA specialist. This company has developed a class 2a medical device in the dental industry and are in need of a consultant that can support with writing their technical documentation from scratch. 


  • Support/advise the team on writing technical documentation/reports from scratch.
  • On vs off site: flexible; 2 days per week at the office 



  • Must have strong EU MDR knowledge from an RA perspective (technical files and reports)
  • +10 years experience (flexible) in the Medtech sector withing RA domains (ISO13485 understanding)
  • Ideal if have experience a Class IIa dental device
  • Languages: English (Dutch is a nice to have)
fulltime position

Start Date: ASAP (March 1st ) 

Duration: 6 months (extension possible)