QA Validation Technical Writer

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

Please call Michael O'Connor today for further information on 091-452410 or email [email protected]


CareerWise Recruitment (