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Validation Engineer

  1. East
United Kingdom
  1. Contract
Competitive
  1. Commissioning, Qualification and Validation
25678ZD

This vacancy has now expired

Validation Engineer - Autoclaves - SIP - Global Pharmaceutical company - 11 month contract - South Leinster 

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.
Requirements:
  • 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.
Please apply today for immediate consideration.

The candidate must have the rights to work in the location stated in the job advert.

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