Vacancy: Regulatory Affairs Specialist -Medical Device – On Site – Ireland

Right now, we are working on a wide range of projects with companies all over the world.  Our consultants, at our head office in Ireland, in the UK and on site with clients are assisting companies as they navigate the ever changing regulatory demands that are being faced by manufacturers.

As part of our ongoing growth we are eager to recruit a regulatory affairs professional with experience in the medical device sector.  The successful candidate will work initially on a specific client project in the Cork/Tipperary area and will be on site 3 or 4 days per week.

Our team is working with our client on a range of projects at their site and the role holder will get the opportunity to work on issues such as new product development, regulatory compliance and more.

The role will initially be offered on a 12 month contract basis and there is scope for the role holder to work remotely/from home as the project progresses.

If you would like to find out more about the project then please contact Brian Cleary at Acorn Regulatory on 00353 52 61 76 706 or email:  brian.cleary@acornregulatory.com