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QC Laboratory Technician

  1. Ireland, West
Carlow
  1. Contract
Competitive
  1. CAPEX Projects
34812wr

This vacancy has now expired

QC Laboratory Technician - Shift - Pharmaceuticals - 11 Month Contract - €19-23/hour 

Do you want to be involved with exciting Pharmaceutical projects?

When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require a QC Laboratory Technician.

This a fantastic opportunity to be involved with the critical investment projects both on-site and remotely.


Role Summary:
  • Movement of materials across the network.
  • System transactions including movement and shipping of samples across QC labs within the network.
  • Knowledge and experience using systems such as GLIMS, LIMS, and SAP beneficial.
  • Inspection of primary packaging
  • Participate in writing/revising/ rolling out accurate operational procedures, training materials and maintenance procedures for various Quality systems; ensure all work is carried out in line with same.  
  • Where applicable, review, approve and trend test results. 
  • Peer review other analysts’ documentation, ensuring QC Right First Time KPIs are achieved. 
  • Participate in QC daily meetings and ensure effective communication of testing progress, deviations etc. 
  • Ensure that all Quality Systems within the department are adhered to on a daily basis. 
  • Complete all documentation in compliance with GMP and GxP standards.  
  • Problem solving to get to root cause of issues. 
  • Provide support with audit/inspection requirements to ensure department compliance/readiness. 
  • Collaborating with others by sharing your skill set and expertise. 
  • Drive continuous improvement, perform root cause analysis on system failures e.g. FMEA, Fishbone diagrams, 5 why's etc, 
  • Drive compliance with Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good manufacturing Practices (cGMP) in the performance of day-to-day activities and all applicable job functions, including maintenance of accurate records.

Experience, Knowledge & Skills
  • 1 - 3 years’ experience in the Pharmaceutical, Biopharmaceuticals industry or a similar operating environment which includes experience in a Quality function.
  • Previous Analytical Experience
  • Demonstrated ability to work independently and fully realise improvement initiatives with a moderate level of guidance.
  • Good communication, interpersonal skills, and ability to work across teams.

If this role is of interest to you, please apply now!  

 #LI-CH3
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