Location:
Cork
Role:
Contract
Contract Length:
1 year
Details
We are seeking a QC Analyst to join our Equipment Team in Quality Control, Cork.
This role is critical in supporting day-to-day laboratory equipment activities, ensuring compliance with GMP standards and maintaining operational excellence.
If you have strong technical skills in equipment maintenance, calibration, and vendor management, this is an excellent opportunity to advance your career in a dynamic pharmaceutical environment.
Key Responsibilities
Coordinate and schedule vendors for laboratory equipment preventative maintenance (PM) and calibration (CAL) activities onsite.
Manage offsite calibration of laboratory equipment and ensure timely return.
Complete equipment calibrations in line with task cards and governing procedures.
Utilize CMMS (GMax) system to manage work orders and calibration schedules.
Troubleshoot laboratory equipment and perform corrective maintenance.
Escalate QC equipment-related risks and implement mitigations.
Conduct periodic system reviews for existing laboratory equipment on GxVal.
Support introduction of new equipment and re-qualification efforts following corrective maintenance.
Lead investigations related to equipment deviations from procedures.
Perform system administrator duties for standalone laboratory equipment (e.g., method setup, account creation).
Complete GVault change controls, CAPAs, and tasks promptly.
Write or revise GVault procedures as required.
Implement LEAN and 5S initiatives and participate in QC Operational Excellence programs.
Experience
Minimum 3 years' experience in pharmaceutical operations.
Ability to coordinate vendor maintenance and calibration services, including review of PM/CAL documentation for laboratory equipment.
Strong troubleshooting skills and capability to perform corrective maintenance on laboratory instruments.
Proficiency in managing work orders and schedules using CMMS (GMax) system.
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