Job Description
A Validation Engineer is required for a leading biopharmaceutical client based in Athlone, Ireland. This is an initial 12-month contract position.
Responsibilities:
* Prepare documentation and monitor progress for technical projects and validated status of Thermal Systems equipment.
* Conduct validation risk assessments to determine testing requirements for equipment changes or new equipment.
* Support sustaining and project validation activities across Drug Substance and Drug Product Areas.
* Maintain hardcopy records in Document control archive, including reconciliation of Documentation.
Requirements:
* 5 years+ relevant experience working in a Validation role in the Pharmaceutical / Biotechnology industry.
* Good knowledge of EN285 and kill kinetics of Stem Sterilization systems.
* Strong technical capabilities, communication skills, teamwork abilities, and initiative.
Key Skills:
* Stem Sterilization
* CTUs thermal mapping
* VHP (Vaporized Hydrogen Peroxide decontamination systems)