A Regulatory Affairs professional, with 12 years experience in European Regulatory Affairs at GlaxoSmithKline. Experience in various therapy areas (Respiratory, Oncology, Biotechnology, Anaesthesiology) and at all phases of the product life-cycle from early stage development to post-marketing line extensions. Key capabilities: regulatory strategy, advising global product development teams, evaluating data and preparing submission documentation. Member of TOPRA (The Organisation for Professionals in Regulatory Affairs).A motivated and positive individual, with good organisation, planning and interpersonal skills.Enthusiastic to return to Regulatory Affairs following a career break with family and caring responsibilities and an extended period of living abroad (in the happiest country in the world!).