Our client is a commercially successful Generics Company with a large variety of Products across many Therapeutic areas. This role is Pan-European in geographic scope. Managing a small team, you will be adept in CMC from in-coming Dossiers/MAA's through to Post marketing: Variations and Renewals; National Submissions/MRP or DCP; Labelling, PIL's and SmPC's. Technical and Strategic advice on new and existing products. We are seeking a candidate with 4 to 6 years experience.
If you are interested in this, or any other Regulatory Affairs opportunity, please call the Key People Regulatory Affairs team on 01727 811 634 or email on: regs@keypeople.co.uk