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CAPA / Deviation Specialist - Solid Dose/Tabletting - GMP

  1. Dublin
  1. Contract
  1. Compliance / Quality Assurance
Date Posted05 Nov 2019

This vacancy has now expired

Would you be interested in working within a state of the art Tablet Manufacturing facility in Dublin? Do you have good experience investigating deviations & CAPA's within an Oral Solid dose environment? If the answer is yes I have a contract role for you!

We are looking for a CAPA /Deviations Specialist to clear a current backlog of deviations & drive continuous improvements to the facility.
The role will involve:
  • Conducting investigations to ensure deviations will satisfy QP and agree CAPAs accordingly
  • Implementing necessary changes and process improvements
  • Close out Deviations and agree CAPAs accordingly
  • Implementing necessary changes and process improvements to ensure elimination/significant reduction in the frequency of similar deviations occurring
  • Work Closely with Manufacturing Supervisors to drive continuous improvements
To be successful for this role we are looking for the following:
  • Experience of working within an OSD/Tabletting GMP facility
  • Experience with: Investigating & closing deviations, CAPA’s, change controls, OSD tabletting equipment (granulation, drying, compression, coating)
  • Experience with Change Controls
You must be happy to work in Dublin for the next 6 months+.

Call me for further information on this project or apply directly through our website!

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

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