Reference #: 259309
This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following
Plan, design and execute work/experimental programmes to further the course of Discovery and Development Projects / programmes and enable key decisions, in particular using mass spectrometry (both LC-MS and GC-MS qualitative).
Demonstrate a sound practical understanding of mass spectrometry and processes, procedures used in mass spectrometry.
Contribute to regulatory dossiers and author/review expert reports.
Comply with the requirements of Quality, Safety and GSK policies and procedures and ensure that GSK intellectual property is protected.
Ability to contribute to and effectively work within matrix teams and with colleagues in other divisions and also colleagues in same divisions e.g. NMR.
Self-motivated flexible approach with good organisational skills and ability to communicate in a scientific manner.
Working knowledge of GxP requirements, SOPs and policies.
Appropriate knowledge of regulatory requirements as applied to the drug development process.
Operational knowledge of laboratory/plant equipment.
Why you?
<<Volver a la información del trabajo