Regulatory and Clinical Affairs Manager, Surrey, Medical Devices, Regulatory and Clinical Affairs Manager
This company is a specialist manufacturing and supplying joint replacement orthopaedic products to the healthcare industry and has been established for the last 30 years. Due to recent expansion they now have an exciting opportunity available for a Regulatory and Clinical Affairs Manager.
As the Regulatory and Clinical Affairs Manager you will be responsible for the operation ad management of the companies regulatory and clinical affairs systems.
Other duties will include:
-Managing regulatory and clinical affairs department and staff
-Participating in NPD process
-Authoring global regulatory and clinical investigation submissions
-Supporting other departments in regulatory assessments of proposed changes
-Interfacing with notified bodies and FDA
-Conducting training
-Overseeing reclassification processes
-Developing, implementing and maintaining regulatory standard operating procedures
The suitable candidate will ideally be educated to a Degree Level (or equivalent). Experience of management within regulatory and clinical submissions within the medical device industry is essential for this position. Membership of a professional body is highly advantageous, but not essential for this role.
Within this growing organisation you will receive a fantastic salary and benefits package. On going development to further enhance your skills is also provided.
