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LIMS Project Analyst

LIMS Project Analyst

LocationGlattpark-Opfikon,, Switzerland
Business SectorBiotechnology
Contact email
Job ref23139
Publishedabout 1 month ago
LIMS Project Analyst
Calling all talented professionals craving an exciting career move! Here's your chance to join a thriving biotech in Dublin, Ireland. We are looking for a LIMS project Analyst to join a dynamic team.

Job Summary

The LIMS Project Analyst is responsible for ensuring that the effective deployment of LIMS Labware V8 at TILGC, aligned with industry best practices and to meet Takeda local expectations. This includes proactively developing, implementing, LIMS Master data to support manufacture, testing, and release of products

Key responsibilities:
  • Configuration or modification of LIMS setups, including microbiology or QC Analytical methods, product specifications, schedulers, standards & reagents, COA's, Label and printer setup, and associated LIMS Master Data.
  • Creation and verification of LIMS Master Data as required.
  • Development of Test Scripts/Test Protocols for formal LIMS test execution as required.
  • Execution of informal and formal verification testing of the configured LIMS solution in collaboration with Computer Systems Validation (CSV) project resources.
  • Hosting facilitated review workshops with users to walk them through the configured LIMS, making updates prior to design completion and testing.
  • Supporting end users in terms of training materials and execution, troubleshooting during hyper-care stages, and escalating issues to IT or LIMS Administrators.
  • Contribution to the development of LIMS Configuration/Design Specifications and Design Note documentation.
  • Assisting with LIMS Hardware setup in collaboration with DD&T.
  • Analysing user requirements and LIMS design in collaboration with business users and associated team members.

Key requirements
  • Bachelor’s degree in Life Sciences, IT or a related scientific discipline.
  • A minimum of 1 years LIMs administration / Master Data Building.
  • Experience working in finished product pharmaceuticals/biologics, including analytical chemistry, quality assurance, quality control, development, and/or manufacturing areas. Specific experience in cell therapy is an advantage.
  • Thorough understanding of quality systems and cGMP's.
  • Hybrid available

Practicalities:
  • Location: Dublin, Ireland
  • Start-date: ASAP
  • Contract duration: 18 months – with a high chance of extension

If this piques your interest, don’t miss out!
Send your CV to Khanyi Mabena at k.mabena@panda-int.com or contact her on +31 2020 44502.