Validation Engineer
- East
- Contract
- Commisions, Qualification and Validation
With global demand for their life-changing oncology treatment increasing; one of our global pharmaceutical clients is looking for Validation Engineers to join their team to support a €500 million expansion project in Leinster.
This is a fantastic opportunity to work on a state-of-the art fill-finish facility and the company’s first stand-alone vaccine and biologics plant outside the US.
Essential Duties and Responsibilities for this role include, but are not limited to, the following:
- Act as validation SME on the equipment within sterilisation – Autoclaves and SIP of vessels.
- Providing technical and validation oversight to process, design and project delivery teams
- Technical review and approval of Commissioning protocols, Qualification protocols and Validation protocols executed by vendors, cross functional groups and/ or validation counterparts.
- Minimum two years’ experience in the pharmaceutical industry and commercial product manufacturing.
- Knowledge of cGMP
- SME on Equipment Validation on SIP / Autoclaves
- Use of temperature mapping equipment such as Lives/ Kaye etc.
- Fill-finish experience is always a plus.
The candidate must have the rights to work in the location stated in the job advert.
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