Description
Role – Cleaning Validation Engineer – MultipleType – 12 month contract
Location – Co. Limerick Ireland
Key Responsibilities:
- 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 including:
- Completion of summary report upon completion of initial protocol execution.
Key Requirements:
- Proven Cleaning Validation experience in the bulk bio industry/pharmaceutical or medical device
- Experience in Document Preparation and Execution
- Experience in developing and implementing grouping strategy documents for cleaning studies.