Job Description
A Validation Technical Writer is required by Careerwise recruitment to work with our Limerick biotech client on a 12-months 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
5. Relevant 3rd Level Degree.
6. Minimum 2 years relevant industry experience.
7. Experienced Technical writer.
8. Experience in Deviation and investigation writing and data review.
9. Experience in Validation specifically SIP/ CIP validation.
10. Experience in SIP/ cleaning validation results reporting review beneficial.
11. An understanding of how manufacturing and SIP/ CIP Validation equipment works.