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National Research Council of Canada seeks a Technical Officer, Upstream Production (USP) to support the Production team at the Clinical Trial Material Facility. The role covers technology transfer through GMP manufacturing of vaccines and biotherapeutics, contributing to clinical development for SMEs.
The incumbent will document experiments, maintain aseptic GMP conditions, and ensure SOP compliance in a fast-paced lab environment, driving quality and reliability in production processes.
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Priority may be given to the following designated employment equity groups: women, Indigenous Peoples* (First Nations, Inuit and Métis), persons with disabilities and racialized persons*.
* The Employment Equity Act, which is under review, uses the terminology Aboriginal peoples and visible minorities.
Candidates are asked to self-declare when applying to this hiring process.
OrganizationalUnit:Human Health Therapeutics
Classification:TO-3
Duration: 2 years
Language Requirements:English or French
Work arrangements:
At the NRC, we recognize that Indigenous candidates may have important connections to their communities and you may be eligible for an exception to this work arrangement. Alternative work arrangements may also be considered to accommodate candidates as required. To learn more about these options, please contact the NRC Hiring team using the contact information below.
We are looking for a Technical Officer, Upstream Production (USP), to support the Production team at the Clinical Trial Material Facility. The Technical Officer would be someone who shares our core values of Integrity, Excellence, Respect and Creativity.
The successful candidate will play an important role within a team in charge of the upstream production process of promising biotherapeutics and vaccines, from the technology transfer to the GMP manufacturing. The effort of this USP team will directly contribute to the clinical development of vaccines and therapeutic candidates for Canadian small and medium-sized enterprises (SME’s). Responsibilities of the candidate will include the provision of technical assistance in the preparation and the conduct of GMP productions, recording, and compiling scientific data, maintaining clean room and process equipment in a highly controlled environment.
This technical officer position would appeal to someone who has a passion for working in a controlled laboratory (GMP) environment, contributing to and following established standard operating procedures, efficiently document experimental and manufacturing activities and results in a dynamic and fast-paced environment.
Applicants must demonstrate within the content of their application that they meet the following screening criteria in order to be given further consideration as candidates:
Bachelor in Sciences, Biotechnology, Engineering or related field.
Collegial diploma combined with relevant and significant experience may be considered.
Each of the following is considered an important asset:
Reliability Status
For a Reliability Status, verification of background information over a period of 5 years is required.
Candidates will be assessed on the basis of the following criteria:
NRC employees enjoy a wide-range of competitive benefits including a robust pension plan, comprehensive health and dental coverage, disability and life insurance, office closure at the end of December, and additional supports to enhance your well-being throughout your career and beyond.
Please direct your questions, with therequisition number (26353) to:
Closing Date: 12 November 2026 - 23:59 Eastern Time
*If you are currently a term or continuing employee at NRC, please apply through the SuccessFactors Careersmodule from your NRC computer.