Description
You are the CSV Engineer looking after validation process for the overall project.
- Experience in GxP Risk Management/current regulations
- Deliver the validation to the company in best practice terms
- End to end full life cycle design to handover
- Documentation/reporting/templating/blueprinting
Immediate interviews - day rate or fixed term contractor wanted
9-13 months contract
Skills/Experience:
- 3 - 5 years in a Computerized Systems Validation role (CSV).
- Excellent technical English verbal and written skills
- CSV experience in an established QA/IT function preferably in the pharmaceutical/healthcare industry
- Strong knowledge of GAMP5, CSV, Project Life Cycle and GxP Regulations
- Experience drafting, reviewing and/or approving validation documentation VMP, URS, RA, IQ, OQ, PQ, UAT, SAT and VSRs.