Job Title: Regulatory Affairs Manager
Company: Gilead Pharmaceutical
Job Type: Full Time
Qualification: BA/BSc/HND
Location: Lagos, Nigeria
Job Field: Administration / Secretarial
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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
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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
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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.
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