A QA Validation Specialist (cleaning validation) is required by Careerwise Recruitment to work for our Limerick based biopharma client.
Role of this position
- Taking Cleaning Validation samples alongside Upstream/Downstream processing.
- Generating and Executing Validation Protocols.
- Capable of managing a large program, so project management skills would be necessary.
- An excellent understanding of how manufacturing/Cleaning Validation/Cleaning equipment works.
- Understanding of baseline studies for new equipment.
- Generate/review/Approval of CV protocols.
- Generate Reports.
- Maintain and update Cleaning Validation Plan.
- Schedule of cleaning activities with Manufacturing.
- Experience in aseptic technique.
- Experience in Validation specifically cleaning validation.
- Experience in assessment of cleaning issues during study runs.
- Experienced Technical writer.
- Experience in Deviation/Change control writing.
Please call Michael O'Connor today for further information on 091-452410 or email firstname.lastname@example.org
CareerWise Recruitment (In Search of Excellence)