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QA Validation Technical Writer, Limerick
Client:
CareerWise Recruitment
Location:
Limerick, Ireland
Job Category:
Other
EU work permit required:
Yes
Job Reference:
dd8835cc880d
Job Views:
87
Posted:
21.01.2025
Expiry Date:
07.03.2025
Job Description:
Job Description
A QA Validation Technical Writer is required by Careerwise recruitment to work with our Limerick based biotech client on a 12-month contract position.
Role of this position
1. Execution of SIP/ cleaning and continuing validation protocols.
2. Writing and approving Deviations/ GMP documents.
3. Technical writing experience in writing site reports.
4. Generate/review/Approval of SIP/ CIP protocols.
5. Generation of Summary Reports.
6. Assessment of SIP/ CIP issues during study runs and closeout of deviations.
Job Requirements
1. Relevant 3rd level degree.
2. Minimum of 2 years experience working in a GxP environment.
3. Preferable to have experience in a commercial Biologics Manufacturing site.
4. Experience in SIP/ cleaning validation results reporting review beneficial.
N.B. It is essential that you hold a valid working visa for Ireland.
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