Deviation Investigator

Ireland is a hive of activity for the Life Sciences Sector at present with global players setting up new / expanding existing manufacturing facilities all over the Country. An exciting opportunity has arisen to work via Quanta on the client’s side for a global Pharmaceutical organisation on one of their existing manufacturing facilities in County Dublin.

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. 

For further information on this role, please apply with a copy of your up to date CV today!

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