Pharma QC Inspector: In-Process QA & Audits

Ccl Label Ireland Ltd; Dublin; On-site; EUR 33,000 - 40,000; Full time

Job summary

CCL Label Ireland Ltd invites applications for a QC Inspector in the Quality department, with immediate start. The role involves in-process QC checks on printed product using an Eye C proofiler, final QA release, logging non-conformances, weekly spot checks and audits, verifying revisions, and assisting in investigations.

Candidates should have a third-level qualification in Engineering or Science or at least two years in QC, be fluent in English, proficient in MS Word and Excel, and possess

Qualifications

• 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.
• Have a good working knowledge of MS Word and Excel.

Responsibilities

• 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 & “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.

Skills

Fluent English

Attention to detail

Reporting skills

Reliability

Education

Third level qualification in Engineering or Science

Minimum 2 years QC experience

Tools

MS Word

MS Excel

Job description

CCL Label Ireland Ltd invites applications for a QC Inspector in the Quality department, with immediate start. The role involves in-process QC checks on printed product using an Eye C proofiler, final QA release, logging non-conformances, weekly spot checks and audits, verifying revisions, and assisting in investigations.

Candidates should have a third-level qualification in Engineering or Science or at least two years in QC, be fluent in English, proficient in MS Word and Excel, and possess