Job description Posted 14 February 2019

Description:

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 records.

Working to agreed deadlines and maintaining records to reflecting project status. responsible for highlighting potential delaying factors promptly to line management and sharing knowledge of regulatory documentation and procedures with others to assist in problem solving.

Proactively pursuing process improvement and sharing of best practice.

Required Skills

CMC experience :good written and oral communication and networking skills.

Demonstrate ability to focus and work with attention to detail.

Demonstrate ability to retain critical information.

Be aware of the contents of a marketing authorization application.

Demonstrate team working and effective time management skills.

Be a dynamic and highly motivated individual

Establish strong relationships and liaise effectively with GSK sites worldwide.

Be proficient in the use of IT packages such as Word and excel.

Demonstrate problem solving skills

Additional information about the process

All profiles will be reviewed against the required skills and experience. Due to the high number of applications, we will only be able to respond to successful applicants in the first instance. We thank you for your interest and the time taken to apply.a