Description
LIMS Administrator/LIMS SME (Laboratory information management)
Location: Weybridge - Defra
Rate: £525/day (out of scope)
Duration: 6 months
REF: PSR1JP
Clearance Required: BPSS
The Role:
- Performing computerised laboratory systems administration duties. access management, role permissions, system audit trail review, setup of new tests and optimisation of existing configuration as required.
- Mining data from software applications used for investigations, reporting, metrics and trending
- Researching and evaluating emerging technologies; leading and implementing software development projects to support operational improvements.
- Ensuring that appropriate documentation is available for regulatory compliance via preparation and revision of relevant operational and validation documentation for laboratory computerised systems
- Perform helpdesk functions for more complex problems in the laboratory, including problem tracking, analysis, resolution, escalation, coordination and training.
- Planning and managing the delivery of validation projects and procedures to meet current GxP guidelines, ISO/IEC 17025 standards, industry best practice and company policy
- Formally reviewing validation protocols, reports and procedures
- Processing and managing quality records including change controls, deviations,
- Record and report results using good record-keeping in compliance with GLP and/or ISO/IEC 17025
- Performing computerised laboratory systems administration duties. access management, role permissions, system audit trail review, setup of new tests and optimisation of existing configuration as required.
- Mining data from software applications used for investigations, reporting, metrics and trending
- Researching and evaluating emerging technologies; leading and implementing software development projects to support operational improvements.
- Ensuring that appropriate documentation is available for regulatory compliance via preparation and revision of relevant operational and validation documentation for laboratory computerised systems
- Perform helpdesk functions for more complex problems in the laboratory, including problem tracking, analysis, resolution, escalation, coordination and training.
- Planning and managing the delivery of validation projects and procedures to meet current GxP guidelines, ISO/IEC 17025 standards, industry best practice and company policy
- Formally reviewing validation protocols, reports and procedures
- Processing and managing quality records including change controls, deviations,
- Record and report results using good record-keeping in compliance with GLP and/or ISO/IEC 17025
To apply for this role please submit your latest CV or contact Aspect Resources