Regulatory Affairs Specialist
Biotechnology Life Sciences
Location Newcastle upon Tyne
Salary Up to £24,000
We have an ideal opportunity for a Quality Assurance/Regulatory affairs individual to join an exciting and innovative medical device company in Newcastle, initially on a 12 month contract.
As a Regulatory Affairs (RA) Specialist, you will be responsible for supporting the registration of company products globally. Maintaining medical device files, technical files and device master records in preparation for regulatory submissions in various markets globally. You will also be responsible for, product renewals and promoting the continuous improvement of regulatory activities.
- Previous experience of quality or regulatory work within the life science sector
- A Degree qualification (or equivalent) in a life science or technical discipline, although it’s not essential
- Strong communication skills and be computer literate (MS Word and Excel are essential), and you’ll need to be reliable, resourceful and can capable of accurate, quality work
- Knowledge of medical devices and IVD regulations (ISO:13485) would be ideal
Apply now with your CV, and feel free to contact Owain at CY for more information 07851 246839.