- South East
- £25,000 - £30,000 DOE
- Non-Laboratory & Other Scientific Roles
About this job
Interested in moving into Quality Assurance? An exciting opportunity has arisen to join a dynamic QA team in an expanding GxP pharmaceutical testing company!
Working in a well-established 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 and the routine checking of analytical data.
Candidates currently working in the Quality Control laboratory environment seeking a move into QA are encouraged to apply. Outstanding communication and attention to detail is essential.
This is an exciting opportunity to join a renowned pharmaceutical contract research organisation – apply now to be considered!
Key words: quality, assurance, control, QA, QC, GMP, good manufacturing practice, GxP, GLP, GCP, documents, data, pharma, pharmaceutical, biopharmaceutical, HPLC, Cambridge, Cambridgeshire, Hertfordshire, VRS6641HQPlease note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website