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QC Laboratory Technician

  1. Midlands (Ireland)
  1. Contract
Competitive
  1. CAPEX Projects
31-01-2024
33222

This vacancy has now expired

QC Laboratory Technician - Bioharma - Carlow, Ireland - 11-Month Contract 

With worldwide demand for their life-changing oncology treatment increasing; one of our global pharmaceutical clients is looking for a QC Laboratory Technician to join their team to support multiple capital projects taking place onsite.

This is a fantastic opportunity to work on a state-of-the art fill-finish facility and the company’s first stand-alone vaccine and biologics plant outside the US. 


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! 
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