Senior Sterilization Engineer

Job Overview

Are you ready to jumpstart your career with a rapidly expanding company where the culture is one that promotes internal advancement?

Have you worked in the medical device or pharmaceutical industry with experience specific to ethylene oxide sterilization cycle development and maintenance?

If so this could be the job and company that you have been looking for!


Rapidly growing Multi-national healthcare company in Galway currently recruiting for a Sterilization Engineer. This truly is a great place to work with a company that is headquartered in Galway (so the big decisions are made here as opposed to the US!) The company really believe in promoting from within (42% of all roles filled last year were internal promotions) so you will have loads of opportunity to progress your career and there has been millions invested in the plant over the past 2 years. With over 120 people having been recruited in 2018 the plan is to continue growing rapidly for the next 5 years.

This is a company that fully support YOU and YOUR long term career goals. They offer full educational support, defined benefit pension, parking, healthcare and an annual bonus designed to reward hard work and hitting targets. This is a place where achievement is recognized and internal progression opportunities are very much available.


As Sterilization Engineer you will work closely with Product Development Teams and / or external customers to plan and execute Sterilization Validation Activities. You will also support key sterilization programs such as sterile load process review and revalidation activities.

Some of the key duties for this exciting role would include:
*Creation and approval of Sterilization Validation Protocols and Reports

*Support Design Service Project Teams with respect to validation of product in approved cycles.

*Management of process deviations, NCRs and CAPAs related to Sterilization Processes

*Knowledgeable of the associated Quality System requirements and interpretation of same ISO/FDA/AAMI related to sterilization.


You will hold a relevant level 8 3rd level engineering degree with 3 yrs.+ demonstrated experience in the medical device or pharmaceutical industry with experience specific to ethylene oxide sterilization cycle development and maintenance.

You will be familiar with regulations and standards published by FDA, USP, AAMI, ANSI, ASTM, and ISO as well as being well versed in the operation and maintenance of environmentally controlled manufacturing and testing facilities.

Sounds like your cup of tea? To apply, click the button!
Or if you just have some questions about the job or want to have a chat call Feargus on 086 020 2554 or connect with me on <> or <https://twitter./>

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