QC Specialist

QC Specialist

  • Location:

    WH, Ireland

  • Sector:

    Engineering & Life Sciences

  • Job type:


  • Contact:

    Simona Morelli

  • Contact email:

    [email protected]

  • Contact phone:

    0164 985 37

  • Job ref:


  • Published:

    about 1 month ago

  • Expiry date:


  • Startdate:


  • Consultant:


You have 2+ years of experience in performing calibration and maintenance activities in a GMP laboratory setting and you are looking to take the next big step in your career? Then look no further, I have the perfect opportunity for you!
This is a one of a kind job opportunity as a QC Specialist III in a fast paced and constantly growing pharmaceutical company.
Their business is growing and they need someone like you to join their QC laboratory support group. You will be reporting into the Laboratory Automation Specialist.
This is a 12-month FTC (full-time) job based in Co. Westmeath.
What will you do in this job?
  • You will be responsible for the coordination and scheduling of all calibration and maintenance contracts & activities for laboratory equipment in QC & Micro laboratories.
  • You will be responsible for the review of vendor calibration and maintenance records and supervision of vendors when onsite
  • You will be responsible for the troubleshooting, tracking and remediation of laboratory equipment issues.
  • You will be responsible for maintaining calibration/maintenance vendor approval process for QC laboratory in conjunction with relevant QA function.
  • You will be responsible for the writing of Protocols and Procedures as required and periodic review of existing SOP's.
  • You will perform continuous assessment of USP and EP in regards to laboratory equipment calibration requirements.
  • You will identify new systems and/or develop existing systems with a view to increase compliance and/or increase efficiencies with Laboratory services.
What do you need to be successful in this job?
  • You hold a degree in Science/Engineering or related discipline.
  • You have 2+ years of experience in a similar role in a GMP pharmaceutical regulated work environment.
  • You have experience in maintaining calibration/maintenance activities in a lab setting.
  • You have an understanding of USP and EP requirements and guidelines for equipment calibration.
  • You have experience in writing and updating SOPs.

The Next Step for you:

Interested in this role? Please send your CV to SIMONA MORELLI at Next Generation Recruitment by clicking on the Apply button!

Not ready to apply just yet? Meet with our recruiters here or get some inspiration to update your CV there.

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