QA Validation Specialist

4 weeks ago


Dublin, Dublin City, Ireland i-Pharm Consulting Full time

QA Validation Specialist

Co. Meath, Ireland

Contract until end of 2025

Our client, a global biopharmaceutical leader, is looking for a QA Validation Specialist III to join their team in Dunboyne. This is a fantastic opportunity to bring your quality assurance and validation expertise to a cutting-edge facility, ensuring compliance and operational excellence in a dynamic, regulated environment.

What You'll Do

In this role, you will:

  • Provide QA oversight for validation and digital data quality (DDQ) activities
  • Review and approve validation documentation, change controls, deviations, and SOPs
  • Support qualification and validation of equipment and computerised systems
  • Contribute to internal audits, risk management, and continuous improvement initiatives
  • Ensure alignment with cGMP, regulatory guidelines, and site procedures

What We're Looking For

  • A degree in science or engineering (postgraduate preferred)
  • Minimum 5 years' experience in QA/Validation in pharma or biotech
  • Solid knowledge of validation lifecycle and computer system validation (CSV)
  • Familiarity with GMP systems such as Veeva Vault, SAP, TrackWise, or Kneat
  • Strong communication, problem-solving, and project management skills
  • Experience with regulatory inspections (FDA, HPRA, EMA) is a big plus

This is a great chance to be part of a supportive and forward-thinking quality team where your expertise will make a real impact.

Interested? Apply now to play a key role in ensuring quality at a world-class biopharma site.

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