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Regulatory Affairs Specialist - Medical Devices - North West
My client is leader in the development of medical devices, with offices in numerous global locations. They currently have a requirement for a Regulatory Affairs specialist at their site in the North West.
This role will be responsible for the regulatory affairs function of the business, managing worldwide registrations, product approvals, and product dossiers. It will also work to maintain internal processes, ensuring departments work closely together to ensure regulatory requirements are met in a timely manner. The Regulatory Affairs Specialist will also have managerial responsibility for a Regulatory Affairs Associate and one other junior member of staff.
Candidates should have extensive previous experience of handling regulatory affairs activities within either a medical devices or pharmaceutical organisation. This should include dealing with worldwide regulatory procedures, and knowledge of drug-device combination products. Any experience of managing small teams would be desirable.
If you are interested in this position, and match the specifications above, please apply online or for more information contact Dannielle Robbins on 0161 839 2400 (quoting reference Y2012DR).