We are looking for a Deviation Investigator from either a Quality or Validation background with experience working in Solid Dose Pharmaceutical Facilities. You will play a key role specialising in closing out Deviations and CAPAs to help the existing team clear a backlog of outstanding investigations.
For this position, you will be resposinle for:
- Full lifecycle hands-on Deviation Investigation experience (including being responsible for closing investigations and CAPAs)
- Conducting Deviation Investigations with Manufacturing environment and operations to ensure deviations and Investigation Reports will satisfy QP's and agree CAPAs accordingly.
- Implementing necessary changes and process improvements to ensure elimination / significant reduction in frequency of similar deviations occurring.
- Work Closely with Manufacturing Supervisors and CAPA Specialist to drive continuous improvements.
Republic of Ireland
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