Regulatory Affairs Executive

South West England
£45 - £58 per hour
25 Jan 2013
22 Feb 2013
Joseph Dykes
Full Time

This is a great opportunity for some one with 2-3 years experience in Regulatory Affairs with the Medical Device sector.

Main responsibilities;

  • Develop and update design dossiers and technical files.
  • Conduct risk management activities
  • Knowledge of regulatory impacts and carry out registrations in relevant territory's
  • Assist current team on regulatory procedures

Key skills / Qualification

  • Ideally an engineering / Biological science background to degree level.
  • Understanding of Regulatory Affairs industry. Knowledge of fillings and submissions in one or more of the following territory's; EMEA, USA, Canada, Australia, Japan, Korea, China, India, Brazil.
  • Understanding of main markets and 93/42/EEC M5

If you believe you are suitable for the role, know someone who is or would like some more information, contact me ASAP.

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