Fancy a new role in Documentation control? Compliance? Our Client is a market leader in the manufacture and development of GMP products and they currently have requirement for a QA administrator. The role is north east of England in Yorkshire and is temporary The Role will require the following activities o To prepare, compile material specifications. o To transcribe information from source documents into a prescr...
An excellent opportunity is available for a temporary Analytical Chemist to work on an initial temporary contract for six months but there are excellent opportunities for progression within this organisation. The role is varied and involves performing analysis and reporting results in accordance with cGMP requirements for laboratory operations. You will support method validation programs and carry out analysis using HPLC, GC a...
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