The NRC is building a new permanent, GMP-compliant clinical trial material facility (CTMF) at its
Royalmount Avenue site in Montréal. When complete, this facility will be used to manufacture vaccine
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 two (2) Consultants Quality Assurance,
Information technology (IT) infrastructure and computerized system (CSV) validation actively participates
in all stages of the implementation and validation lifecycle for an IT infrastructure and other processes
related computerized systems in compliance with applicable Health Canada, European and FDA
regulations, policies and procedures and Government of Canada security requirements.
Consultant will provide quality assurance support during the implementation and validation phases of the
Project, in an agile configuration for:
? IT infrastructure
? Data integrity
? As an option: GMP compliance support and training to IT Team and automation Team
