experience as a computer system validation / quality assurance for life sciences company regulated by the FDA is preferred...
Responsibilities: Ensure control of systems, processes and products through facilitation of CCRB. Represent site and provide impact assessment for global changes at Global CCRB Monitor and track external audit/inspection commitments to ...
Responsibilities: The Senior Specialist is responsible for supporting the Quality Engineering group from a Subject Matter Expert (SME) standpoint in accordance with Client policies, standards, procedures, and Global cGMP. Functional resp...
Responsibilities: Ensure control of systems, processes and products through facilitation of CCRB. Represent site and provide impact assessment for global changes at Global CCRB. Monitor and track external audit/inspection commitments to...
Responsibilities: Working under the direction of the Team Lead / Project Manager, the senior statistical programmer conducts programming activities for a trial, early phase project, indication, or publication activities. Lead at least on...
Responsibilities: Operational Activities. Executes equipment calibration, preventative maintenance, performance verification and repair activities in laboratory and manufacturing areas. Supervises vendors for calibration, preventative m...