Regulatory Affairs Engineer, Medical Device, Medical Devices, Surrey, Regulatory Engineer
This global organisation has been established since 1991 and specialises in manufacturing and supplying joint replacement orthopaedic products to the healthcare industry. Due to recent expansion they now have an opportunity for a Regulatory Affairs Engineer to join their highly successful team in Surrey.
As the Regulatory Affairs Engineer you will be responsible for supporting the global regulatory submissions. This will include maintaining and implementing the company’s regulatory affairs systems.
Other duties will include:
-Supporting all global regulatory submissions
-Authoring global regulatory submissions
-Conducting training to other employees on regulatory matters
-Assisting with the reclassification process
-Developing, implementing and maintaining regulatory standard operating procedures
The suitable applicant will ideally be educated to a Degree level (or equivalent). Previous experience of working in regulatory and clinical submissions within the medical device industry is essential for this role. You will also have experience of working within a quality position.
The successful applicant will receive an excellent salary and benefits package, with on going career progression opportunities.
