Description
Biomedical Client based in Scotland currently have a contract vacancy for an experienced Validation Engineer with good experience of CIP (Clean in place)Manufacturing sterile injectibles, we need a good Validation Engineer to execute the Clean in Place Validation studies.
We are looking for a good CIP Validation Engineer to execute the study by liaising with both production & QC Laboratories for the analysis of samples, collation of results and writing of reports. Some SIP qualification work may be involved.
This contract role is for a mid july start with a 8.5 hour day, 5 days a week.
To be successful for this role we are looking for the following skills/experiece:
* Validation Engineer - CIP (SIP nice to have
* Acccustomed to wlrking within a secondary / fill finish pharma environemnt
For further details please call today.