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Regulatory Affairs Consultant

Join NNITs Life Science Professional Services department and become our new Regulatory Affairs consultant. We are on the forefront of advising clients in Denmark and across Europe on the latest changes within Regulatory Affairs and their IT impact on the Life Science industry. 

We offer you the opportunity to operate in the sweet spot where domain expertise meets patience needs and where you can make your mark on some of the most exciting IT projects within the Life Sciences industry.     

You will join NNIT who has just been nominated as Denmark’s second most attractive IT workplace and the most attractive within the IT consulting area.     

Your responsibilities as Regulatory Affairs Consultant  

In the Life Sciences Professional Services (Regulatory Affairs) team you will join an exciting international department with highly skilled colleagues that have a deep understanding of the pharmaceutical industry and the ability to bridge this knowledge with IT.   Working closely with Danish and European clients you will use your experience from Regulatory Affairs to advise and assist Life Sciences companies in a vast array of projects spanning from process optimization and business adaptation to new legislative changes to vendor selection for new IT solutions within the area, implementation of electronic document management systems, labelling and regulatory information management systems.  Part of the job involves business development activities related to the development of new offerings that will support our growth within Life sciences. The job will in turn include close collaboration with a multitude of stakeholders within NNIT where your knowledge form the pharmaceutical industry will strengthen our companies' strategic aspirations in Life sciences.    If you have the right profile and the ambitions you will be able to be the important link between business and IT and get the opportunity to convey knowledge and intelligence in an international setting. These engagements may lead to Keynote Speaker sessions at conferences and authoring of relevant articles about Regulatory Affairs.   

You will be part of the international Life Science Advisory Team  

The Life Sciences consulting unit is an ambitious team of approximately 60 people working from Switzerland, Germany and Denmark, 20 people of which are part of the Danish team you will join. We appreciate openness, honesty and a winning attitude. We expect you to have these personal skills and also that you are able to quickly integrate with the other team members.   Our customers expect us to know about upcoming trends and regulatory changes, and that we are at the forefront in terms of advice and solutions. Your career will include continuous training and competence development to support our department and your personal ambitions.   The team is part of the NNIT Solutions division responsible for advising our customers on business and technology as well as designing and implementing IT solutions and applications.   

Your qualifications and experiences  

You hold an MSc degree in Life sciences or IT with 3-5 years of experience from the pharmaceutical industry (preferably Regulatory Affairs). You have a good understanding of IT and you are able to bridge your professional experience from the pharmaceutical industry with IT. You must have a curious nature and interest in new technologies.   It is an advantage if you have experience with business processes and regulatory requirements within Regulatory Affairs and that you have a good overall understanding of IT solutions within this area.   You are used to advice and built trust on all levels, and you might have gained this experience from a past job within the management consulting area.   Fluent in oral and written English is a must. Some travel must be expected.

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