If you've got Global or above country CMC RA experience in the life sciences industry you’d like to hear about a great role with a well established and highly regarded research based pharma company I’d love to hear from you.

Our client has a fantastic reputation both from a product perspective and as a place to work.  With a range of well established and innovative pipeline products they have a balanced portfolio and enjoy consistent growth.  From a reputational perspective they have an incredible name both in terms of the quality of their products and their ethical conduct.

This role will report into the Global Regulatory Affairs team but will be based in the UK, so you'll need to be a UK resident to be suitable for this role. 

You'll be responsible for the management of the CMC regulatory submissions and dossiers for products under Geographical Expansion and/or Product enhancement (line extensions/renewals/major variations), with the supervision of the manager. 

If this is something of interest to you then please send your details to me via the "apply" link or email me on Lorna@bluepelican.com.