Computer Systems Validation (CSV) Engineer – Dublin

SimoTech is looking for experienced Computer System Validation Engineers for a number of exciting BioTech roles in Dublin. These are attractive career opportunities working on the client side. Candidates must have at least 3 years experience in the pharmaceutical/life sciences industry.

The roles offer excellent remuneration with extended contract durations.

Role/Opportunity
  • Support department activities, including but not limited to the preparation of Validation/Qualification plans, risk assessments, URS, Traceability Matrix, testing, data migration, SOPs and Change Controls.
  • Ensure that the computerised systems are in full compliance with both regulatory requirements and with company policies and procedures.
  • Support the resolution of deviations and/or errors and provide quality guidance on GxP regulatory requirements.
Experience/Background
  • 3rd level Science / Engineering degree required.
  • Minimum of 3 years relevant CSV experience in either the Biotech or Pharma industry.
  • Thorough knowledge of cGMP regulations related to CSV, including 21 CFR Part 11 and EU GMP Annex 11 is required.
  • Strong knowledge of computerised system development life cycle.
  • Experience of coordination of quality documentation and in particular qualification/validation documentation.
  • Validation experience with ERP, MES, DCS, LIMS, PLC and Quality Systems.
  • Ability to present validation documentation during the IMB, FDA and Corporate audits.
Only Candidates eligible for work permits for Ireland/EU can be considered for this role.