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QC Inspector

  • Image for Employer
    CCL Label Ireland Ltd
  • Image for Job Ref
    Ref: #JOB-2439350
  • Image for Location
    Multiple Locations
  • Image Position
    No of positions: 2
  • Image Part Time
    Paid Position
  • Image Hours per week
    39 hours per week
  • Image for Euro
    36605.00 Euro Annually
  • Image for Published
    Published On: 27 Mar 2026
  • Image for Closing
    Closing On: 24 Apr 2026

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Location Image
Multiple locations
CCL LABEL IRELAND LIMITED, UNIT B14, Ballycoolin Bus Pk, Dublin 15, D15 PX27
A permanent position has become available in the Quality department for a QC Inspector who will work as part of the QC Team as per the job spec below with an immediate start.
	Carry out in-process QC checks on printed product, including using an Eye C proofiler. 
	Final QA Release on all Pharma jobs plus other customers requiring certs of conformances and ”problem” jobs as directed by QA Manager.
	Log internal non-conformances and issue to department responsible and participate in the investigation process.
	Carry out weekly spot checks and internal audits.
	Verify and process product revisions.
	Buddy check pharma orders & approve new pharma art works when required.
	Help out investigating quality issues and take part in quality improvement projects. 
The position will be shift based, alternating weekly 
Week 1: 6am – 2.30pm Mon - Fri 
Week 2: 2.30pm – 11.00pm Mon - Thurs
Please ensure you have your own transport or are you on a bus route to meet the early start and late finish.
Salary offered: €36,605 based on candidate qualifications and experience.
Site Address:
CCL Label Ireland Ltd. Unit B14, Ballycoolin Business & Technology Park, Ballycoolin Road, Dublin 15, D15 PX27, Ireland
Candidate’s must: 
	Be fluent in English 
	Be available to start immediately
	Have a third level qualification in Engineering or Science or a minimum of 2 yrs relevant industry experience in a QC Role. Full industry training will be provided for the successful candidate.
	Have a good working knowledge of MS word and excel
	Good levels of attention to detail are required at all times
	Diligent, reliable and good reporting skills.
Experience working in a GMP environment would also be an advantage.
Full training will be provided for the successful candidate.
All interested candidates should forward their CV to Trisha Carney by email to tcarney@cclind.com who will organise an interview and discuss the position further.
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