Are you looking for a new and exciting opportunity? We have the perfect one for you! The Gene Transfer Facility quality system ensures compliance of the facility with cGMP and governs manufacturing and testing requires excellent data management to allow traceability and analysis. This is a prerequisite for auditing, addressing non-conformance and quality improvement. Data analysis and correlative studies also contribute to the quality improvement approach by laying the cornerstone for assay revision and implementation of new technologies. The QC Supervisor is responsible for planning QC activities in the CTCEF lab including developing new assays, SOPS, preparing data reports, infusion, and validation. The role is responsible
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