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OverviewWe are seeking experienced quality professionals to support a major pharmaceutical manufacturing client in Greenville, North Carolina. This engagement focuses on strengthening quality oversight, manufacturing compliance, remediation activities, and inspection readiness efforts within a regulated GMP environment.Consultants will join an esta...
We are seeking an experienced IT Validation Specialist to support validation and compliance activities for GxP-regulated systems within a highly regulated life sciences environment. The position will play a critical role in ensuring that IT and automation solutions are implemented using risk-based validation methodologies while maintaining complian...