Description
In this great opportunity you will be joining a rapidly growing pharmaceutical company which is a leader in the Swiss Pharma market. You will play an integral part in the Regulatory team and have the opportunity to work in a international and challenging environment where your creativity, initiative and expertise are more than welcome. Working in the areas of oncology, neurology and respiratory diseases you will surely have the chance to make a difference in the lives of thousands of patients.As the new Regulatory Affairs Manager you will be responsible for:
- Preparing and Submitting MA applications for new submissions as well as variations and extensions
- Develop strategies for products to be submitted
- Responsible for products portfolio
- Answer inquiries from Authorities
- Build and publish information on medicines
The ideal profile will include:
- A pharmacist or scientific degree
- Experience in Regulatory Affairs ideally with NCE submission experience
- Good knowledge of Swiss Environment
- Excellent MS Office knowledge and experience in e-ctd publishing
- Very good German and English (French a plus)
If you are interested in this role or other Regulatory Affairs positions within Switzerland then feel free to get in touch with me at matthew.lillywhite(@)realstaffing.com or on and I would be more than happy to provide you with further details. I look forward to hearing from you.
<p>To find out more about Real please visit <a href="http://www.realstaffing.com">www.realstaffing.com</a></p>