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 Execution of SIP/ cleaning and continuing validation protocols.
Writing and approving Deviations/ GMP documents Technical writing experience in writing site reports.
Generate/review/Approval of SIP/ CIP protocols Generation of Summary Reports Assessment of SIP/ CIP issues during study runs and closeout of deviations JOB REQUIREMENTS Relevant 3rd level degree.
Minimum of 2 years experience working in a GxP environment.
Preferable to have experience in a commercial Biologics Manufacturing site.
Experience in SIP/ cleaning validation results reporting review beneficial N.B.
It is essential that you hold a valid working visa for Ireland