Great opportunity to join a global Pharmaceutical company on a 12 month contract basis as a Cleaning Validation Engineer.
Main responsibilities:
* Collaborating with manufacturing to ensure the CIP/SIP and dirty holds are to the correct times and samples are taken.
* Developing and Executing Validation Protocols.
* Generate/review/Approval of protocols.
* Maintain and update Cleaning Validation Plan.
Qualifications & Preferential experience:
* Degree in Engineering / Science discipline.
* 3+ years relevant experience.
* Experience in aseptic technique.
* Experience in Gowning for IOS7/ISO8.
* Experienced Technical writer.
* Experience in Deviation/Change control writing.
* Understanding of baseline studies for new equipment.
If this exciting role is of interest to you please get in touch on 021 2300 300 or by email.
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