Full Description
Contract: 6 months (to start, potential to extend)
JOB DESCRIPTION
Our client is a global immunology company committed to improving the lives of individuals who have severe autoimmune diseases with their novel antibody-based medicines.
They are currently seeking a Computer Systems Validation (CSV) resource to author SOPs, create work instructions, assist in writing validation and quality plans for non-GXP
systems.
This role reports into the Sr Manager of IT Quality and Validation.
This client uses Veeva Quality Docs and therefore experience with Veeva is a plus.
Required Skillset
General Computer System validation experience
Veeva validation experience is a plus.
Knowledge in Non- GXP computer system SDLC (commercial, financial systems etc..) is a plus.
SOP writing.
5-7+ years of CSV experience