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Location: County Cork, Ireland
Salary: €40,000 – 50,000 + Benefits
Fed up of working on one project and want to work across multiple pharmaceutical projects simultaneously? Look no further. I am currently supporting a global client with offices in the USA and Ireland who offer automation solutions to a range of industries all over the globe who are now looking for a validation engineer with an eye for detail to work on some of their most highly-valued customer projects.
As a validation engineer, you will be responsible for developing and delivering CSV and C&Q outputs within pharmaceutical manufacturing facilities. This will include (and not limited to), validation planning, user/functional requirements, design specifications, design qualification, testing protocols as well as report writing at every stage of the process.
Ideally, you will be currently working as a validation engineer or CSV engineer within a pharmaceutical/biotech/medical device setting delivering validation tasks at every step of the process.
This vacancy is being advertised by Advanced Resource Managers. ARM is a specialist talent acquisition and management consultancy. We provide technical contingency recruitment and a portfolio of more complex resource solutions.
Our specialist recruitment divisions cover the entire technical arena, including some of the most economically and strategically important industries in the UK and the world today. We will never send your CV without your permission.
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