Regulatory Affairs Manager - Rare Diseases
Rare Disease products - Marketed product activities - Post approval - London based.
Your new company
I am working with a leading bio-pharmaceutical company who specialise in developing products for patients with rare genetic diseases. They want to employ a Regulatory Affairs Manager to based full tine on site at their office in Central London.
Your new role
This is an EU focused position working on their marketed product portfolio, activities will include preparing regulatory submissions to the EU and Switzerland, new license applications, renewals, annual reports, labelling and variations. The Regulatory Affairs Manager will also contribute to product development strategies when required.
The Regulatory Affairs Manager will also be required to manage agency interactions, participate in local process improvement initiatives and participate in Regulatory team meetings. These responsibilities are not limited and there will be other requirements of the Manager.
What you'll need to succeed
To be suitable for this role, you should have:
A degree in a Life Science discipline or equivalent
Experience working within Regulatory Affairs
EU submission experience
Experience working with branded products
Post marketing experience
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call Natasha Calisi at HAYS now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.