Validation Engineer

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Location: carlow

Type: Contract

Rate: Negotiable

Contact: mtreacy@asset.ie

Reference: MT5101

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


Responsibilities:

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.

Qualifications/Experience:

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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