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  • Location

    Leiden, Netherlands

  • Job title:

    eLIMS administrator

  • Sector:

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  • Startdate:


The Company 
This organisation is a world-leader in the research & development and production of biotechnology and pharmaceutical products. Their main focus is the production of biologic products and vaccines. For this specific role, you will join the Covid-19 project. 

Role Description 
As eLIMS administrator you will be responsible for translating documents, like stability plans, specification sheets and sample plans to clear eLIMS Master Data and configurations. 

  • Translation of relevant documents to eLIMS Master Data. 
  • Build eLIMS Master Data and ensure the right quality. 
  • First point of contact of relevant stakeholders like Release and Stability Coordinator, and Stability Scientists. 
  • Act as an SME for Quality during regulatory inspections, internal and external GMP audits. 
  • Ensure compliance with cGMP standards. 

  • MLO-4 or HLO, with experience in quality and laboratory systems (cGMP, SAP, LIMS). 
  • 3+ years of experience within the pharmaceutical industry. 
  • Excellent communications skills in English. Dutch is a strong plus. 
Other Information 
For more information please contact Carla Garcia at or +31 (0) 658 98 01.