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 Generation of Summary Reports.
Writing and approving Deviations/ GMP documents.
Maintain and update Cleaning/ SIP Validation Plan.
Schedule of Cleaning/ SIP activities with Manufacturing.
JOB REQUIREMENTS Relevant 3rd Level Degree.
Minimum 2 years relevant industry experience.
Experienced Technical writer.
Experience in Deviation and investigation writing and data review.
Experience in Validation specifically SIP/ CIP validation.
Experience in SIP/ cleaning validation results reporting review beneficial.
An understanding of how manufacturing and SIP/ CIP Validation equipment works.