Biotechnology Validation and Documentation Specialist

1 week ago


Limerick, Limerick, Ireland TN Ireland Full time
About the Role
We are looking for an experienced Validation and Documentation Specialist to join our team. As a key member of our QA team, you will be responsible for executing SIP/ cleaning and continuing validation protocols, writing and approving deviations/ GMP documents, generating/reviewing/approving SIP/ CIP protocols, and producing summary reports. Your attention to detail and analytical skills will ensure that all documentation meets regulatory requirements.

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