Cleaning Validation Engineer

‐ Onsite

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Keywords

Project Manager Interface Reporting Manager

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.

Duties

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.

Experience:

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.

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