Senior Regulatory Executive: Biopharma

Description

• Knowledge and experience in Biopharma
• Preparation of high quality, Chemistry manufacturing and control (CMC) detailed regulatory documents using varied information sources.
• Liaising closely with other GSK personnel to ensure accuracy of such documents.
• Working together with other groups to ensure that ongoing projects are captured in these documents and that any changes are recorded.
• Ensuring that project work proceeds according to agreed deadlines and maintaining status records.
• Responsible for highlighting potential delaying factors promptly.