Regulatory Affairs Manager at Gilead Pharmaceutical Limited

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