Meg holds a B.Sc. in Science from UCC and an M.Sc. in Biotechnology from UCG.

She has also been a practising QP for over 20 years with experience in aseptically processed and terminally sterilised dosage form, as well as oral solid dosage and topical creams and ointments.

Meg has extensive CMC regulatory experience, having worked in both pre-approval and post approval of products registered in the EU, US and the rest of the world. She also has extensive API experience, having held Quality and Regulatory positions in both biotechnology and small molecule manufacturers.