- Taking Cleaning Validation samples alongside Upstream/Downstream processing.
- Working closely with manufacturing to ensure the CIP/SIP and dirty holds are to the correct times and samples are taken.
- Experience in aseptic technique.
- Generating and Executing Validation Protocols.
- Experience in Validation specifically cleaning validation.
- Experienced Technical writer or Experience in Deviation/Change control writing
- Execution of cleaning validation protocols.
- Experience on writing and approving Deviations/ GMP documents.
- Technical writing experience in writing site reports.