Job Summary:
The role involves reporting directly to the Validation Manager and performing IQ/OQ activities to ensure equipment compliance with relevant international standards. The position will also require nationwide travel.
Key Responsibilities:
* Perform validation and servicing of cleanrooms, LAFs, isolators, and laboratory equipment in pharmaceutical, medical device, and healthcare facilities.
* Generate detailed validation and service reports.
* Approve and sign off on completed projects.
* Collaborate with the team to follow up on validation leads.
* Communicate and coordinate with suppliers to ensure project requirements are met.
Qualifications:
* Hold a third-level education qualification or relevant trade certification.
* Proficient in using MS Office applications.
* Possess a full, clean driving license.
* Demonstrate strong communication skills.
What’s next?
* Apply now by clicking “Apply Now” or contact me at +353 21 461 5740 or email pkiely@zevas.ie
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