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QA Specialist

  1. East
Denmark
  1. Contract
Competitive
  1. Compliance / Quality Assurance
02-11-2021
26231ZD

This vacancy has now expired

QA Specialist - Global Pharmaceutical Company - 8 and 11 month contracts - South Leinster 

With global demand for their life-changing oncology treatment increasing; one of our global pharmaceutical clients is looking for QA Specialists 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:
  • Provide Quality support to IPT production teams to ensure cGMP standards are maintained.
  • Perform timely reviews of batch documentation / investigations / reports highlighting and assist in the resolution of concerns commensurate with the risk.
  • Conduct, report and display of Quality right first time, audit readiness metrics weekly to ensure continuous audit readiness and cGMP compliance.
Requirements:
  • At least three years’ experience in the pharmaceutical industry within a quality role.
  • Technical knowledge of Sterile Manufacturing
  • Operational experience of quality systems in a dynamic manufacturing environment eg SAP, Trackwise, MES
If you are interested initially, please apply now for immediate consideration and further information.

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

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