Responsibilities
Implement regulatory strategies to forecast potential issues and flag these through clear and effective communication
To oversee and manage the post CE approval products to guarantee an effortless integration of new products following launch
Uphold a current knowledge of industry standards to distribute to direct reports and project teams
To confirm submissions are of high standard and compliant with industry requirements
Experience Required
Must have proven experience in handling direct reports
An Extensive knowledge of Regulatory Affairs within the medical device industry
Has participated in post and pre market submissions
CE Marking experience
Requirements
Must be a clear communicator
Efficient in time management to be able to handle multiple projects at one time
A positive attitude to ensure effective collaboration within the team
Ideally degree educated with vast experience working with medical devices
go to method of application ยป
Interested and qualified candidate should send their CV’s to gileadpharm@gmail.com Only shortlisted applicants will be contacted.
Apply via :
gileadpharm@gmail.com
