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Location: Co. Clare, Ireland
Salary: €Competitive + Attractive Benefits
The medical device sector is a major (if not, the main!) contributor to the Irish economy and off the back of 3-4 years of solid, continued growth (in headcount and factory space), an automation solutions provider is looking for a number of people to support on the delivery of a range of customer projects. As I always say, the demand for automation and the associated engineering skill sets is high, don't fall behind the curve!
As a validation engineer, you will be responsible for developing and delivering documentation in accordance with industry standards for medical device automation. 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, technical author, technical writer or documentation specialist within a highly-regulated engineering environment and looking to diversify their skill set in to medical technology / pharmaceuticals.
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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