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| Job Location | Liverpool |
| Education | Not Mentioned |
| Salary | Salary negotiable |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Contract , full-time |
Quality and Validation Specialist£18PH PAYELiverpool6 Month ContractCpl Life Sciences are partnering with a global pharmaceutical company that focusses on vaccines, the purpose of the Quality and Validation Specialist is to support investigations to previous and new. The perfect candidate will need to have experience writingup reports using relevant templates supplied by the client.Key responsibilities. Writes method validation protocols and reports independently Executes method validations and lab studies independently Subject matter expert in Microbiological Assays Knowledge and experience of PCR assay desirable Supports QC lab as SME for moderately complex investigations Leads standard method transfer, validation and verification projects Attends project related meetings as departmental representation as required Solves a range of routine and moderately complex problems Analyses possible solutions using standard procedures Receives a minimal level of guidance and direction May influence others within job area through explanation of facts, policies, and practicesIf this role is of interest to you please apply within or send your CV to