Regulatory Affairs Consultant

Would you like to work with regulatory strategies and help bring interesting products to market? Here, you can grow as both a specialist and people manager, and we promise to make real investments in your career.

Join a leading medtech consultancy
Medicologic is a leading Danish medtech consultancy and engineering company. You will be based at our headquarters in Ørestaden, Copenhagen, where you will collaborate with management and customers as well as a team of dedicated professionals. As Consultant in the Regulatory Affairs & Quality Team, you help introduce new and innovative products to the market, and this is an excellent opportunity to develop your skills, as we want to invest in your career and build on your potential. Learn more about us at

Take on several exciting projects
This is a truly versatile position, and you will get to meet and work with several different customers and types of companies. Your mission is to bring our customers’ products to market by applying your knowledge within e.g. approval, testing of medical devices and processes required for product registration. As part of this, you work with hands-on RA & QA assignments and, if possible help generate new opportunities in your communication and interaction with our customers. If you have the potential and interest, you may take on the opportunity to lead and develop the RA & Quality Team.

This could be the career move
This is a unique opportunity to apply your regulatory affairs insights and embark on a new career path as a consultant. At Medicologic, we offer an inspiring, positive and professional work environment where you will get to develop both as a specialist and potentially as a leader. This means participating in specific courses to expand your knowledge of some areas as well as conferring with skilled colleagues to ensure we grow as a team and as a company. We all look forward to meeting you and beginning this journey with you.

To succeed in this position, you have:
– A relevant pharmaceutical or engineering degree
– A few years of experience from regulatory affairs and quality assurance
– Some knowledge of CE mark approval, CE testing for Medical Devices (MDD) as well as FDA, 510K registration and PMA
– Good English skills both written and spoken

As a person, you look forward to using your regulatory insight in a business context, and with your excellent communication skills, you have no problem interacting with customers and colleagues. At the same time, you might be interested in taking on the challenge of people management, and you know that you possess the drive to ensure project progress.

For further information about the job, please contact Recruitment Consultant from Jobindex, Peter Høgh, on +45 38 32 33 97.

Your application
The application deadline is 20 January 2016. Please apply by using the “søg jobbet online”-button here.
We look forward to hearing from you.