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CSV Engineer 1155



SimoTech currently requires a CSV Engineer for a pharmaceutical project based in Dublin. Candidates must have at least 3+ years’ technical experience of working in a busy manufacturing environment, preferably pharmaceuticals.

Key Responsibilities

  • Support department activities, including but not limited to the preparation of Validation/Qualification plans and strategies, risk assessments, URS, 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.


  • 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 qualification/validation documentation.
  • Strong technical writing and communication skills.

What SimoTech Can Offer

  • Role provides a high degree of autonomy to allow the successful candidate to reach their full potential.
  • Long term project opportunity.
  • SimoTech can facilitate these positions as a staff engineer or contract engineer.
  • Competitive staff or contract rates.

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