Quality Engineer, Life Sciences

From £40,000 to £50,000 per annum
08 Oct 2016
19 Oct 2016
Contract Type
Fantastic opportunity with a world leading innovative organisation Do you have a strong background in compliance, validation and quality? Have you worked in the pharmaceutical industry for at least 5 years? Are you aware of processes such as CAPA and root cause analysis? Then this could be the role for you Working as part of a team you will fulfil an important role ensuring quality standards are maintained, providing validation input & assessment and leading root cause analyses to resolve deviations. You will liaise extensively with various departments to ensure appropriate regulations are upheld (GxP and related). You will also be responsible for training of staff and customers on relevant quality procedures. The ideal candidate will possess: - at least 5 years’ experience in the pharmaceutical industry - experience working in a Quality-related role - strong understanding of GxP regulations and processes such as root cause analysis and CAPA - excellent communication skills - strong problem solving abilities Contact VRS today for more information on this outstanding new role Key words: CAPA, corrective and preventative action, process improvement, root cause analysis, quality, ISO, regulation, regulatory, accreditation, FDA, validation, quality, engineer, manufacturing, technical, QA, deviation, GxP, GLP, GCP, GMP, good manufacturing practice, Cambridge, Cambridgeshire, East Anglia, VRS5287LC This job was originally posted as www.totaljobs.com/job/66832732