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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