Description
A UK based biologics manufacturer is looking to appoint an experienced CSV Engineer to join the team.Role:
*Development and execution of qualification & validation of Information Systems software.
*Development of life cycle documents necessary to address the validation lifecycle (Planning, Risk, Implementation, and maintenance of the validated state).
*Provide assistance, where required, with the preparation/testing of validation protocols and all associated documentation for equipment/systems.
*Review/Approval of all Computer Systems/Software Validation Documentation.
Experience
*A Bachelor’s degree in Computer Science, / Computer Engineering
*Prior experience in working with cGMPs and Quality Systems is essential.
*Experience of working as a CSV Engineer in the Pharmaceutical / biopharmaceutical industry is essential.
*Have the ability to communicate IT/Validation concepts/strategies to project teams.
This UK based opportunity would suite an experienced CSV professional, if this you please apply today!