International Pharmaceutical Manufacturer requires a Senior Regulatory Affairs Executive to be a key member of the team, providing advice on the regulatory requirements for assigned new products, the submission of variations, renewals and marketing authorisation applications in the UK, Ireland and other overseas territories and monitoring all of the above through to grant. You will be representing the Regulatory Department at both internal and external meetings as directed.
You will need an appreciation of all aspects of the workings of the pharmaceutical industry, an ability to present the Company’s interests in a professional and authoritative manner and experience with information technology relating to regulatory affairs. You will have the ability to organise your own workload with a minimum of supervision, and have an exceptional eye for detail. We will also need you to have a degree or equivalent in life sciences, substantial experience in regulatory affairs and ideally you will be a member of TOPRA (Organisation for Professional in Regulatory Affairs).
You will be joining a truly international Pharmaceutical company, offering a wide range of company benefits.