LIMS Administrator

**Full-time remote work availabe**

A global Biopharmaceutical company require 2 x LIMS administrators to work within their QC Department during an extremely busy time. Being a CDMO this is an extremely dynamic role as they respond to their customer’s needs.

We require 2 x LIMS Administrators/Specialists to support the department as an existing resource moves across to support a new upgrade programme taking them from LIMS version 6 to version 8.

This will be to support the routine operation within a very dynamic department within a busy CDMO, coding LIMS Basic, addressing support requests, and interfacing with Users.

The persons should be able to code in LIMS Basic and have had several years of experience working in a GMP environment. Working language is English. 

• Setup complete LIMS Master Data including Analysis, Product Build and Static data
• System administration and maintenance of LIMS (Labware LIMS v6)
• User access administration, Label printer setup - optional
• Analyse root causes of issues and provide appropriate resolutions based upon troubleshooting
• Understanding of the ER (EntityRelationship) model – data structure of Labware LIMS to troubleshoot data issues
• Experience in major Labware LIMS modules (i.e., Sample management, Inventory, Lot, Stability), and Instrument interfacing
• Experience in Crystal reports development in LIMS (i.e., critical reports such as CofA, Analytical Reports)
• Perform Change management including drafting IQ, OQ scripts along with defect management following GxP guidelines
• Knowledge of the Pharmaceutical or Biotech industries

For further information please apply!

The candidate must have the rights to work in the location stated in the job advert.

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