Description
A Global Bio Pharmaceutical organisation currently requires an experienced Computer Systems Validation (CSV) engineer to work at their site in South East UK.For this role, we are looking for a CSV Engineer to carry out the validation of an independent monitoring system.
Activity list
-Responsible for ensuring and coordinating support to projects
-Review and approve protocols for IQ/OQ/PQ
-Write qualification status report.
-Managing of deviation
To be successful for this role you will have the following skills/experience
-CSV experience essential
-Experienced with complex validation activities.
-Knowledge of regulatory requirements (GMP, CFR and Eudralex).
-Good communication and organisational skills.