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
7. Relevant 3rd level degree.
8. Minimum of 2 years experience working in a GxP environment.
9. Preferable to have experience in a commercial Biologics Manufacturing site.
10. Experience in SIP/ cleaning validation results reporting review beneficial
N.B. It is essential that you hold a valid working visa for Ireland