SIP / SIP Technical Writer

SIP / CIP Technical Writers - QAV Team - West Coast of Ireland - Biopharmaceutical - 12-month contract 

Ireland is a hive of activity for the Life Sciences Industry at present with no shortage of major expansion/ new build facilities. We have an exciting opportunity for a QAV SIP / CIP Technical Writer to join a project for a global Bio-pharmaceutical organisation with great longevity of employment possibility.

Located within a commutable distance of one of Ireland’s airports, this position would suit both local candidates and those wishing to commute from outside of Ireland.

Who are we looking for?

We are looking for a QAV Technical Writer with SIP/ CIP / cleaning validation experience to join a large Manufacturing facility on the West Coast of Ireland until the end of the year initially with strong chance of 12 month extension thereafter

The ideal candidate will have:

• Experienced in QA Validation activities –
• Execution of SIP/ CIP / cleaning and continuing validation protocols.
• Experience on writing and approving Deviations/ GMP documents
• Technical writing experience in writing site reports.

Key attributes:

• Experienced Technical writer,
• Experience in Deviation and investigation writing and data review
• Experience in Validation specifically SIP/ CIP validation
• Experience in assessment of SIP/ CIP issues during study runs and closeout of deviations
• Experience in SIP/ cleaning validation results reporting review beneficial

For more information on this project / position, please apply with a copy of your up to date CV today!       



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

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