QA Specialist
- East
- Contract
- Compliance / Quality Assurance
With global demand for their life-changing oncology treatment increasing; one of our global pharmaceutical clients is looking for a QA Specialist 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.
- 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
The candidate must have the rights to work in the location stated in the job advert.
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