Description
This huge business has had some internal move around that means there is now a need for a Global Regulatory Affairs Manager to join their successful team in the North West of England. The site in the northwest has 800 employees, 300 of which have Phd's. This position will be reporting in to the Global Regulatory Director.General responsibilities include, but are not limited to;
- The strategic introduction of medical device regulations to new & existing products.
- Engage with notified bodies & regulators about product classification.
- Carrying out product submissions and registrations mainly in the EU & USA
- Gathering scientific data from scientists and advising on best regulatory practice.
- Managing stake holders both internally and externally.
Required experiences;
- Strong background within Medical Devices.
- Working experience and knowledge of regulatory affairs, regulatory strategy product submissions/registrations.
- Experience dealing with notified bodies in the EU andUSA
- Experience with FMCG or oral care would be preferential but not essential.
The role is a fantastic opportunity to get in to a very responsible position in a huge multinational business at a time when new regulations are about to come in to effect
The base salary is £56,000 and there is a car allowance of £7200, the role also comes with a very generous package.
If you feel you have the correct experience then please send me an up to date copy of your CV and I will be in touch shortly to discuss further.
To find out more about Real please visit www.realstaffing.com