This vacancy has now expired
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.
Our client, one of the world’s largest pharmaceutical organisations and one of the top 20 largest pharmaceutical companies in the world by revenue is focussed on developing treatments within
A contract vacancy has arisen for an experienced Materials Scientist. Working with a new state of the art multi-product biologics manufacturing facility in Dublin. We are looking for a
The QC Microbiology Analyst role is a critically important activity in this large pharmaceutical company, you will ensure efficient and effective compliant design, construction, qualification, and
Send us your CV
Our candidates are the cornerstone of our organisation and we are always looking to connect with new professionals who are seeking their next contract assignment or career opportunity.