Overview
Validation/ Maintenance Engineer
Location: Kerry - Onsite
Duration: Full Time Permanent
Industry: Pharmaceutical
Responsibilities
* To be responsible for the overall maintenance and calibration of all manufacturing equipment and instrumentation.
* Responsible for the validation, calibration and maintenance of the Purified Water and WFI systems, the HVAC system and autoclaves.
* Oversee engineering function and ensure PM schedule and Master Validation Plan is adhered to and all associated records updated
* To be responsible for IQ, OQ, PQ for all new and existing equipment.
* To review the Batch Manufacturing Records prior to quality review and final review by the QP in a timely manner.
* To manage, train and motivate production/maintenance operators.
* To monitor, review and improve efficiency and quality.
* Interaction with Production/QA & QC departments.
* Assist with the purchasing and replacing equipment while maintaining high maintenance standards of equipment.
* Maintaining and agreeing service contracts with service providers.
Qualifications
* Pharmaceutical background
* Experience with regulatory audits
* Experience ensuring that the PM/Validation Schedule is adhered to
* Technical writing of paperwork associated with PM/Validations and report writing.
* 3rd level technical qualification in life sciences or similar.
How to apply
For more information, please contact Alan on alan@accpro.ie or click apply now
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