Regulatory Policy Professional

The job

is a unique opportunity to demonstrate your capacity for analysing, responding to, and influencing new regulatory requirements. As an RA Policy Professional, you will conduct impact assessments around new and draft requirements that impact Novo Nordisk regulatory procedures, and you will drive the development of Novo Nordisk responses to these when relevant. You will support the planning and execution of strategic advocacy initiatives around prioritised themes including working with Novo Nordisk representatives in external for a and participating in external working groups yourself. The work will take place in collaboration with colleagues in RP&I and the rest of the Regulatory Affairs through frequent sparring. You will report to the Head of RA Policy & Intelligence and be based in Søborg, Denmark. Qualifications You have an academic degree in Pharmacy or similar and have 3-5 years relevant job experience working in Regulatory Affairs e.g. as part of an RA product development team. The role requires knowledge of regulatory requirements and practices primarily in the European Union, while other markets will be a plus. You have a strategic mind-set and great stakeholder management skills. You are independent, result-oriented, and like to be challenged. You will be expected to have the ability to present complex issues in a clear manner. Excellent communication and presentation skills are required. You must be fluent in written and spoken English. Working at Novo Nordisk It is your skills, your commitment, and your ambitions which help us ensure that innovative products reach patients and improve the lives of many people. In return, we offer you the opportunity to work with exceptionally talented colleagues and a wide range of opportunities for professional and personal development.