Regulatory Affairs Manager & Regulatory Project Planner
The world of medical devices has been flipped on it’s head! – New regulations coming into play have meant more and more opportunities for contract and perm workers to really get stuck in with these fantastic healthcare businesses.
Due to the changing landscape and need for specialists in these areas, my client (a global medical device company) is seeking a Regulatory Manager and a Regulatory Project Planner to join their team based near Watford, UK.
These roles are permanent positions and are for the more experienced RA professionals out there.
The manager position will require someone with 10+ years experience in the Medical Device industry (with enough knowledge of the new MDR to assist with a transition period) and ideally will be someone who has written technical files and worked on CE marking recently. For this role you will also need to be degree educated in a scientific discipline and have good knowledge of EU regulatory guidelines and requirements. If you have FDA experience as well you will definitely be considered a desirable candidate.
On the other hand, the project planner role is more junior and is ideally looking for someone who has a PRINCE2 qualification, Good regulatory experience in Medical Devices, University degree in science or engineering but above all else, someone who is methodical and can take charge of a regulatory project no problem. This role will mainly be focussed on tracking and planning the regulatory projects within the company portfolio (this will include dossiers, international registrations, design history files and technical files).
Both roles are exciting opportunities for someone to really take the next steps in their career and offer very competitive remuneration packages.
My client is looking to fill these roles urgently so please do reach out now and we can get the application in process!
This job was originally posted as www.jobsite.co.uk/job/959924159