I am currently recruiting for a CSV Engineer on a contract basis for a client of mine based in the Norfolk area for a Medical Devices company. They are world leaders in the production of devices to aid respiratory drug delivery.
They are looking for a the ideal candidate to have a strong medical devices background.
The role will involve the development - EU GMP Annex 11, 21 CFR Part 11 and GAMP 5 software review procedures in the Quality Engineering department.
(Usability with a leading towards automated systems), IEC / EN 62304 (Software Development Lifecycle) and ISO 14971 (Risk Management).
The review and develop the SOPs used by the business to ensure compliance with these requirements
Upgrade the company's Technical documentation as far as possible to meet the new SOPs
Location : Norfolk
Start Date: ASAP
Contract Length: 6 Months
If this sounds like something that would interest you then please send an updated version of your CV and I will be in touch.
Alternatively, please pass this on to any relevant persons.
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