Job Description
A Validation Technical Writer is required by Careerwise Recruitment to work with our Limerick biotech client on a 12-month contracting position.
Role of this position
1. Generation of Summary Reports.
2. Writing and approving Deviations/GMP documents.
3. Maintain and update Cleaning/SIP Validation Plan.
4. Schedule of Cleaning/SIP activities with Manufacturing.
JOB REQUIREMENTS
1. Relevant 3rd Level Degree.
2. Minimum 2 years relevant industry experience.
3. Experienced Technical Writer.
4. Experience in Deviation and investigation writing and data review.
5. Experience in Validation, specifically SIP/CIP validation.
6. Experience in SIP/cleaning validation results reporting review is beneficial.
7. An understanding of how manufacturing and SIP/CIP Validation equipment works.
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