We have the pleasure of working with a global leader within the medical device industry and through their continued development and growth we have been asked to help them locate a strong Regulatory Affairs professional to join their European team.
The main objective of this role will be to contribute to the successful regional business goals by supporting the day to day regulatory activities across the region. You will have direct interaction with the local regulatory authorities, with a focus on;
To be considered for this position you will need to be degree educated with at least 3 years post qualification experience within the regulatory field.
Although specific product knowledge is not a requirement, prior working knowledge of the medical device industry is with preferably a solid understanding and working history managing post market activities.
This is a regional position and therefore excellent communication skills will be required along with the occasional need to travel to other business units within the group.