Global Regulatory Affairs Specialist

£55 - £70 per hour
22 Jan 2013
19 Feb 2013
Joseph Dykes
Full Time

This Company is currently going through a re branding process, so needs someone to assist their new products launching in to their current territories, whilst assisting in the global re brand.

General Responsibilities Include,

  • Product submissions inEU,USA,South America,Russia,BrazilandChina. They have 93 markets in total.
  • Assisting in regulatory procedures in whole life cycle of products.
  • Risk management.
  • Technical file writing and reviewing.
  • Assist current team with knowledge of Sterilisation Process, Active Devices, ISO 13485 and the MDD directive.

Required Experiences;

  • 5+ years within Medical Devices
  • Working Experience of Submissions globally
  • Strong Technical File Experience.
  • Engineering Background in design would be preferable but not necessary

Apply now to avoid disappointment, call 02077587322, or apply below

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