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Validation Specialist for Clinical Trial Material Facility | National Research Council · CanPursue
Opportunities
Fit is part of the trial and paid plans.Closed

Validation Specialist for Clinical Trial Material Facility

National Research Council22-58149Federal
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Published
Mar 21, 2024
Respond by
Apr 16, 2024
Latest amendment
—2 amendments

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Description

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

Procurement

Category
Services
Jurisdiction
Federal

Not stated in the notice: procurement type, procurement method, selection criteria, region of delivery, region of opportunity, expected contract period, end user

Requirements and qualifications

Supply arrangement
Not stated in the public notice
Security requirement
Not stated in the public notice
Trade agreements
—
Limited tendering reason
—

Classification

GSIN
—
UNSPSC
—

Amendments

The source reports 2 amendments. CanPursue observed 1 of them with dates.

  • Amendment 2Apr 16, 2024
  • Original noticeMar 21, 2024

Documents

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Contact

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Source

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Source
CanadaBuys
Solicitation
22-58149
Observed
Sep 27, 2026

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