- East Anglia
- £18,000 – £30,000 DOE
- Non-Laboratory & Other Scientific Roles
About this job
An exciting opportunity has arisen to join a dynamic QA team in an expanding pharmaceutical testing company!
Working in a well-established, state-of-the-art facility you will work closely across multiple departments to ensure GMP compliance of laboratory studies and equipment. You will be responsible for creating and reviewing quality documents within the Quality Management System, monitoring validation protocols, undertaking on-site audits, and maintaining KPI’s.
Applications are welcome from QA professionals who have auditing experience within a GMP testing laboratory. Candidates in laboratory environment seeking a move into QA are also encouraged to apply. To be considered for this position you must be meticulous have excellent communication skills.
Apply to VRS now to be considered for this amazing opportunity!Key words: quality, assurance, control, QA, QC, GMP, good manufacturing practice, GxP, GLP, GCP, documents, data, pharma, pharmaceutical, biopharmaceutical, HPLC, Cambridge, Cambridgeshire, Hertfordshire, VRS6093AW