Gilead Pharmaceutical Limited, is recruiting for a suitably qualified candidate to fill the position below:
Job Title: Regulatory Affairs Manager
Location: Lagos
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
Application Closing Date
24th April, 2016.
How to Apply
Interested and qualified candidate should send their CV's to:
gileadpharm@gmail.com
Note: Only shortlisted applicants will be contacted.