Description
A well respected, well known life sciences company that produces pharmaceutical, medical device and also cosmetic products are seeking a Regulatory Affairs Manager position for their medical technology product range. The company are currently experiencing a significant period of growth throughout Europe, and already have a stronghold on the North American market. They plan to expand extensively over the next three years.Within the role, the primary responsibilities include the participation in formulating strategies to optimize product approvals and opportunities of both new and existing products, which will require a broad understanding of regulatory requirements throughout Switzerland and the rest of Europe.
Additionally you will manage all regulatory affairs activities in support of medical device product development and provide labels and obtain appropriate regulatory information to support importing and exporting the companies products. There will be some travel, but not usually more than 10%.
The ideal candidate will be an enthusiastic individual who is looking to play a big part in the journey the company is going on. They should have an educational background in a life sciences discipline or in regulatory affairs and possess between 2-6 years experience in regulatory affairs and vigilance of medical devices. Experience in European Drug Regulatory Affairs is a nice to have.
For further information on this position please contact Ed Bevans at Real Pharma on or email me directly to
If this position doesn't seem to fit your experience perfectly, but you are in the market for a new role, please do not hesitate to contact me, as I also have a number of other job opportunities available.
<p>To find out more about Real please visit <a href="http://www.realstaffing.com">www.realstaffing.com</a></p>