Validation Technical Writer

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.

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 beneficial.
7. An understanding of how manufacturing and SIP/ CIP Validation equipment works.