Description
Excellent opportunity available for an experienced Cleaning Validation Engineer to work for a leading Biopharmaceutical organisation based in Ireland.Main responsibilities
Work with the Area Project Manager/QAV 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 sample submission/results.
Working with the following departments: Manufacturing, Engineering, Facilities, QC chemistry,
QC Microbiology.
Completion of summary report upon completion of initial protocol execution.
Requirements
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.