Consultants will lead or support defined scopes within GMP-regulated environments, managing deliverables, schedules, and stakeholder communications. They will partner with cross-functional client teams to resolve complex issues and ensure operational readiness across various life sciences projects.
The CSV Consultant will support the validation of a GMP-regulated LIMS upgrade by developing validation plans, documentation, and test scripts. They will collaborate with cross-functional stakeholders to ensure system compliance, resolve discrepancies, and maintain inspection-ready documentation.
