Description
Our biopharmaceutical client requires a Cleaning Validation Engineer to join them on a 12 month contract.Main responsibilities
- Completes Document Preparation and Field Execution activities for the initial Cleaning Validation scope.
- Member of QAVAL Team, reporting to the Area Project Manager/QAVAL Specialist.
- Work with Area Project Manager/QAVAL Specialist to develop Cleaning strategies/grouping documents.
- Schedule protocol generation and execution to meet indicated due dates.
- Complete Document Preparation and Execution of these activities.
- Interface with other QAVAL team members and with the following groups to facilitate protocol preparation, execution, troubleshooting, and sample submission/results.
- Manufacturing.
- Engineering.
- Facilities.
- QC Chemistry.
- QC Microbiology.
- Completion of summary report upon completion of initial protocol execution.
- Proven Cleaning Validation experience in the bulk bio industry.
- Experience in Document Preparation and Execution.
- Experience in developing and implementing grouping strategy documents for Cleaning studies.