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QC Inspector

Ccl Label Ireland LtdBlanchardstown, Dublin 15, DublinEURESpublished 09/28/2026
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Nice-to-have:QA/Test

In order to work in Ireland a non-EEA National, unless they are exempted, must hold a valid employment permit. Please review the Eligibility and requirements for an employment permit if you are unsure of your eligibility to apply for this vacancy.

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.

  1. Carry out in-process QC checks on printed product, including using an Eye C proofiler.
  2. Final QA Release on all Pharma jobs plus other customers requiring certs of conformances & ”problem” jobs as directed by QA Manager.
  3. Log internal non-conformances and issue to department responsible and participate in the investigation process.
  4. Carry out weekly spot checks and internal audits.
  5. Verify and process product revisions.
  6. Buddy check pharma orders & approve new pharma art works when required.
  7. Help out investigating quality issues and take part in quality improvement projects.

You will be on alternating shift hours as follows: Week 1 Monday to Thursday 6.00 am to 2.30 pm, Friday 6.00am to 3:30pm Week 2 Monday to Thursday 2.30 pm to 11.00 pm, with 30 minutes for lunch each day and Average weekly hours over 2 weeks shift pattern = 39 hours

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.