Imterim Regulatory Affairs Manager

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 02077587322.

To find out more about Real please visit www.realstaffing.com [1]

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[1] http://www.realstaffing.com/uk