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.