Description
A leading global medical device company are looking for a Regulatory Affairs Specialist on an 3-6 month contract whilst they build their permanent team. They are based in the South East and the sooner the successful candidate can start the better.The successful Regulatory Affairs Specialist is responsible for the implementation of international regulatory strategies, priorities agreed among EEMEA Marketing and country management.
- At least 1-2 years experience in a international organizational business environment
- Prior experience of product registration of Medical device in Europe and EEMEA
- Any experience in a MD area (also operational environment, good understanding of MD business and processes)
- Good understanding European and US FDA regulations and international standards applicable to medical devices industry
If you would like to be considered for this role then please apply with your up to date CV. Remember to pass on to friends or colleagues as we offer referral vouchers for successfully placed referral.
Thanks and kind regards,
Nathan Puxty