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Validation Analyst at Valtera Group Ltd

Position Validation Analyst
Posted 03 Aug 2026
Expired 02 Sep 2026
Company Valtera Group Ltd
Location Galway | IE
Job Type Full Time

Job Description:

Latest job information from Valtera Group Ltd for the position of Validation Analyst. If the Validation Analyst vacancy in Galway matches your qualifications, please submit your latest application or CV directly through the updated Jobkos job portal.

Please note that applying for a job may not always be easy, as new candidates must meet certain qualifications and requirements set by the company. We hope the career opportunity at Valtera Group Ltd for the position of Validation Analyst below matches your qualifications.

Galway, Ireland (on-site)

A leading pharmaceutical manufacturing site is upgrading its LabWare LIMS platform across QC and analytical labs, and building out the team delivering it. This role owns LIMS master data build, digital validation execution, and SOP-to-workflow translation, working directly with QC analysts, LIMS engineers, and QA to get the new system to go-live. It suits an analytical/QC professional who has moved into LIMS implementation work and wants to build on that track record.

What You Will Do
  • Support the LabWare LIMS upgrade by collating instrument calibration, PM, and interface data and building it into LIMS master data
  • Create and verify LIMS master data against approved specifications
  • Execute digital validation test scripts (IQ/OQ/PQ) and support user acceptance testing
  • Translate analytical SOPs and methods into LIMS workflows, components, and calculations
  • Support Empower–LIMS interface testing and data alignment
  • Draft and route SOPs, work instructions, protocols, and reports through the SDLC and change control process
  • Act as a working-level SME between the QC lab, LIMS engineers, and validation
  • Support user migration to the new platform
What We're Looking For
  • Strong working knowledge of chemistry, QC, and analytical techniques (HPLC, UV, dissolution, etc.)
  • Hands-on LIMS experience, LabWare strongly preferred
  • Knowledge of Empower and associated lab systems
  • 1-3+ years in pharmaceutical R&D or QC laboratories in a GMP environment
  • Working knowledge of GMP, FDA 21 CFR Part 11, and EU GMP Annex 11 for computerised systems
  • Strong technical writing skills for SOPs, protocols, and validation reports
  • Comfortable in LIMS, TrackWise, MS Office; SAP and Documentum a plus
  • Self-motivated, detail-oriented, and able to work as part of a small implementation team

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Job Info:

  • Company: Valtera Group Ltd
  • Position: Validation Analyst
  • Work Location: Galway
  • Country: IE

How to Submit an Application:

After reading and understanding the criteria and minimum qualification requirements explained in the job information Validation Analyst at the office Galway above, immediately complete the job application files such as a job application letter, CV, photocopy of diploma, transcript, and other supplements as explained above. Submit via the Next Page link below.

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