The NRC is building a new permanent, GMP-compliant Clinical Trial Material Facility (CTMF) at its site located at 6100 Royalmount Avenue, Montreal, QC. When complete, this facility will be used to manufacture vaccines and other biologic materials for clinical trials, to support vaccine development at the clinical trial stage.
As a member of the multidisciplinary project teams, the Consultant shall actively participate in all stages of the implementation and validation of the CTMF. The Consultant shall determine the content for validation/qualification Standard Operating Procedures which must support Good Manufacturing Practices (GMP) standards
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