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Requirements

Apotech is looking to bring on a Regulatory Affairs Consultant with a specific focus on MDR, to service our clients across Europe and the US.

  • Experience with MDD to MDR remediation projects for medical devices
  • Experience with Technical writing and reviewing technical documents
  • Knowledge of design and risk control processes within a Medical Device Company QMS
  • Experience in reviewing sterilisation and biocompatibility documents for medical devices would be an advantage
  • Excellent organisation and communication skills required
  • Must be able to work off own initiative and be solution-focused

Apply now

  • Your CV
    (2 Mo max, PDF, JPG, DOCX)
    Accepted file types: pdf, jpg, docx.
  • Your cover letter
    (2 Mo max, PDF, JPG, DOCX)
    Accepted file types: pdf, jpg, docx.