Validation Engineer


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Location: carlow

Type: Contract

Rate: Negotiable


Reference: MT5101

Updated: 13/12/2017 17:04:36


Primary responsibilities for the Validation Engineer include the following: Project validation support including conducting equipment performance qualifications (specifically cleaning and sterilization validation)
Authoring project validation master plans; SOP and documentation updates; Authoring validation protocols and final reports, executing validation studies, analysis of validation data; Resolving technical issues encountered during study execution.
This individual will be required to work in a cross-functional team and independently to accomplish validation project objectives.
Be able to work with moderate work direction and is skilled and knowledgeable to the position.


Degree in Science, Engineering or related area.
3-4 years experience working in a Pharma/Biopharma/Med Device/Healthcare manufacturing environment.
Equipment Validation and Sterilization Validation.
Strong technical writing and oral communication skills.

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