Technical Officer, Downstream Processing

Tenure, durée et arrangements de travail

Tenure: Term

Duration: Two (2) years

Language Requirements: English or French

Work arrangements:Due to the nature of the work and operational requirements, this position will require full-time physical presence at the NRC work location identified.

Découvrir les possibilités

Anything is possible at the NRC, named in 2025 one of Canada’s Top Employers for Young People, Top Employer in the National Capital Region and Forbes Canada’s Best Employers!

As Canada’s largest research and innovation organization, our world-renowned research pushes the boundaries of science and engineering to make the impossible, possible. Every day we explore new ideas through innovative research and help companies discover possibilities that impact Canada’s future and the world.

At the NRC, you’ll also discover new possibilities. Our supportive workplace fosters a culture of creativity, welcoming fresh perspectives and innovation at all levels. We value teamwork. You’ll collaborate across multiple fields and with the brightest minds to find creative solutions. Most importantly, you’ll discover what’s possible within you as you grow, make valuable contributions and progress in your professional journey. From ground-breaking discoveries to a life-changing career, discover your possible at the NRC.

Description du poste

We are looking for a Technical Officer to support the Downstream Processing team in our Human Health Therapeutics Research Centre. The incumbent would be someone who shares our core values of Integrity, Excellence, Respect and Creativity.

The Human Health Therapeutics Research Center (HHT) has a mandate to support the country's economic development through healthcare innovations, including novel therapies. The research center has a strong track record of collaborations with industry and is a key player in the prosperity of small and medium-sized enterprises (SMEs). With its primary sector of activity being the biopharmaceutical industry, the portfolio targets Canadian SMEs developing therapeutic products, biologics, or vaccines to address human health needs.

As part of the Downstream Processing team, the Technical Officer will support NRC, other government departments and industry research activities through technical assistance and facility maintenance at our Royalmount facility in Montreal. The incumbent will be part of a multidisciplinary team, providing essential support for ongoing projects and programs involving our industry partners and other government departments and agencies in the area of biotechnology.

The Technical Officer within the Downstream Processing team plays a key role in developing robust and scalable purification processes to enable biologics manufacturing. The incumbent supports early-stage programs by executing and maintaining platform purification activities, contributes to drug development through downstream process development and optimization, and supports clinical trial programs by providing technical support for cGMP clinical batch manufacturing within the Clinical Trial Material Facility (CTMF). This role requires rigorous documentation, strong adherence to established procedures, and effective collaboration with process development and manufacturing teams.

Responsabilités clés

The key responsibilities of the technical officer are the following:

• Adapt and execute platform purification processes in low- or high-throughput formats to achieve target yield and purity of drug candidates.
• Pack and qualify chromatography columns for lab- to large-scale processes and maintain associated column hardware.
• Prepare buffers for small- and large-scale processing in both R&D and GMP environments using scale-appropriate equipment.
• Execute DSP development studies using a QbD approach; demonstrate process robustness and scalability (including impurity/residual clearance and intermediate stability); and scale up processes from bench to pilot scale for GMP manufacturing transfer.
• Provide technical support and assist in cGMP clinical batch manufacturing at CTMF.
• Write batch records and standard operating procedures; maintain detailed records of experimental design, results, and procedures per internal quality standards and regulatory expectations.
  Coordinate procurement of DSP consumables and ensure timely availability to meet project timelines.
• Adhere to occupational health and safety protocols, laboratory security measures, and research confidentiality requirements.

Exigences de sélection

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:

Éducation

Bachelor of Science degree () in biotechnology, biochemistry or a field related to the position.

A Master’s graduate degree () in biotechnology, biochemistry or a field related to the position would be considered an asset.

For information on certificates and diplomas issued abroad, please see Degree equivalency

Expérience

• Significant experience* operating ÄKTA chromatography systems and developing methods using Unicorn software.
• Significant experience* in chromatography column packing.
• Significant experience* in buffer preparation and handling of large liquid volumes.
• Significant experience* in aseptic liquid handling techniques.
• Significant experience* in setting up and operating tangential flow filtration systems, depth filtration, nanofiltration, and sterile filtration.
• Significant experience* in drafting and revising standard operating procedures and batch records.
• Significant experience* in data analysis with MS Excel or similar software packages.
• Experience in biologics manufacturing under GMP environment.
• Experience with a range of DNA and protein analytical techniques, including ELISA, UPLC, and dPCR, will be considered an asset.

* Significant experience is defined as two (2) to six (6) years of experience.

Conditions d’emploi

Reliability Status

For a Reliability Status, verification of background information over a period of 5 years is required.

Exigences linguistiques

English or French

Information on language requirements and self-assessment tests

Critères d’évaluation

Candidates will be assessed on the basis of the following criteria:

Compétences techniques

• Knowledge of basic protein biochemistry and principles of protein/virus purification.
• Knowledge of various unit operations in downstream processing.
• Knowledge of chromatographic separation methods for proteins and viruses.
• Ability to operate and program ÄKTA chromatography equipment.
• Knowledge of drug development pathways and relevant regulatory guidelines.
• Ability to accurately follow, modify, or create Standard Operating Procedures (SOPs).
• Ability to precisely document experiments and communicate effectively both orally and in writing.

Compétences comportementales

• Research Technician/Technologist - Communication (Level 2)
• Research Technician/Technologist - Creative thinking (Level 2)
• Research Technician/Technologist - Results orientation (Level 2)
• Research Technician/Technologist - Teamwork (Level 2)

Profils de compétences

For this position, the NRC will evaluate candidates using the following competency profile(s): Research Technician/Technologist

View all competency profiles

Rémunération

From $66,126 to $91,012 per annum.

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.