Imterim Regulatory Affairs Manager

Oxfordshire  ‐ Onsite
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Keywords

Description

This Market Leading client now have an urgent need for somebody on a contract basis to hit the ground running and support the regulatory department.

This role would involve being the sole go to and advisor for the business in a regulatory capacity for a length of time.

General Responsibilities Include;
  • CE marking of new and re classified products.
  • Technical file writing.
  • Interaction with the MHRA including Declaration Letters.
  • Assistance on Company Branding.


Required Experience;
  • Strong working experience of the IVD industry and the IVD Directive.
  • Proven track record of writing Technical Files and gaining CE mark in previous roles.
  • Previous experience of interacting with the MHRA.
  • Drug Testing and Auditing are preferable but not essential.


My client is looking for someone who is business minded and a good decision maker who can help lead the department.

This particular need is urgent, so to avoid disappointment contact Joseph for more details on .

To find out more about Real please visit www.realstaffing.com
Start date
03/2013
From
Real
Published at
27.02.2013
Project ID:
495579
Contract type
Freelance
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