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IT Lab Analyst

  1. NI & Ireland
  1. Contract
Competitive
26709/ZM
  1. Life Sciences
Date Posted11 Jun 2021
IT Lab Analyst - 11-months+ - Ireland 
  • Provide hands-on end user support, administration, installation and issue resolution for GxP controlled laboratory equipment, servers, desktops and software packages. Perform laboratory upgrades (software, desktop components, etc…), Create/Review/Approve system documentation and author/execute test scripts as needed. 
Role Description 
  • Troubleshoot and resolve complex laboratory technical issues involving software, OS, hardware, network, or scientific equipment setup/interfaces.
  • Perform laboratory equipment, hardware and software upgrades following corporate computer system validation policy and GMP best practices.
  • Represent IT on digital strategies within the QC, MS&T and Manufacturing analytical equipment
  • Work with Global IT teams on LIMS, Empower, and Moda upgrades/enhancements and issue resolutions.
  • Execute routine system administration and maintenance activities as required.
  • Create and/or execute software validation scripts to support laboratory.
  • Create and maintain system documentation including system design specifications, user requirements, functional requirements or routine controlled application change forms.
  • Proactively communicate with laboratory stakeholders and update helpdesk tracking software as necessary.
  • Ensure proper user management process is adhered to for all computerised systems
  • Administer lab system access requests
  • Participates in or leads computerised system software/solution provider audits.                           
QUALIFICATIONS & EDUCATION
  • A minimum of a bachelor’s degree in a technical discipline
  • Prior QC Lab experience with analytical instrumentation qualification and system implementation.
  • Excellent communication skills (written and oral).
  • Ability to multi-task and handle tasks with competing priorities effectively.
  • Strong technical aptitude (i.e. able to read and comprehend technical documentation and execute procedures), global regulatory experience and demonstrated experience interfacing with regulators.
  • Experience with working in a multinational organisation.
  • Experience in delivering training to relevant personnel on the correct application of the site quality system procedures.
 



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

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