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QAV Specialist

  1. Ireland, Midlands (Ireland)
Carlow
  1. Contract
Competitive
  1. Life Sciences
36060
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QAV Specialist - (Hybrid) 2/3 days per week - Carlow - 11-Months 

With worldwide demand for their life-changing oncology treatment increasing; one of our global pharmaceutical clients is looking for a QAV Specialist to join their team to support multiple capital projects taking place onsite in Carlow.

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. 

 Role summary: 
  • Provide quality oversight and direction for the introduction of new products.
  • Conduct quality reviews and approvals of engineering/validation/automation/utilities commissioning and qualification activities.
  • Author, review, and approve protocols and reports for technology transfer, method qualification, and method validation.

Requirements:
  • A minimum of 3-5 years of experience in a quality role, ideally in a pharmaceutical manufacturing environment
  • Quality oversite experience in reviewing and approving documents associated with Equipment Validation, Cleaning validation, Sterilization such as Autoclaves and other equipment like CTU's, Isolators etc.
  • Also looking for Quality oversite of equipment Qualification and knowing how to review and approve the following documents IQ, OQ, PQ, IOC, IOQ's etc.
  • If they have used these systems also would be great KNEAT, IPI, Veeva Vault.


If you are interested, please apply now for immediate consideration and further information.

 #LI-CH3
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