Technical Officer, Quality Control

Overview

Technical Officer, Quality Control Jobs in Montreal, Canada at National Research Council Canada

Title: Technical Officer, Quality Control

Company: National Research Council Canada

Location: Montreal, Canada

Category:

Location: Montreal

Tenure:

Term

Duration: 2 years

Language Requirements: Bilingual Imperative BBB/BBB

Work arrangements:Due to the nature of the work and operational requirements, this position may be eligible for a limited hybrid work arrangement (combination of working onsite and telework).

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.

Discover the possible

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.

The role

We are looking for a Technical Officer, Quality Control (QC) for the Human Health Therapeutics (HHT) Research Centre. The Technical Officer would be someone who shares our core values of Integrity, Excellence, Respect and Creativity.

The candidate will be involved in the control of materials (raw materials, finished products and critical consumables).

The candidate will support quality control activities, with a particular focus on the testing and release of materials, including raw materials, finished products, and critical consumables.

The principal responsibilities will be the following:

Incoming material documentation (specification, material information sheet)

Raw material sampling

Incoming Material management (quarantine, release, OOS investigation…)

Communication with suppliers when required

Final product release management

Coordination with external laboratory and internal teams

Analytical method Validation and/or qualification review for raw material and final product testing methods (review of protocol, data, and reports, follow-up and coordination with external lab)

Stability management (review of protocol, data, and reports, follow-up and coordination with external lab)

Generation of specifications for intermediate and final products, when required

General documentation tasks (Documentation review, SOP generation and revision, data review, purchase of QC material, …)

The candidate will also be involved in:

Environmental monitoring data entry

OOS/OOT investigation

Support to other teams

Improve the QC activities by modifying SOPs, forms, tools, when necessary

Other tasks related to Quality Control

Screening criteria

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:

Education

Bachelor’s degree in science (biology, chemistry, or any other related scientific field).

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

Experience

Significant experience in the pharmaceuticals field within a Quality Control laboratory operating in a Good Manufacturing Practices (GMP) compliant environment;

Significant experience in Biomanufacturing;

Experience in analytical method validation/qualification in biochemistry (ex : SDS-page, ELISA, qPCR, SEC-HPLC, etc..);

Experience in biomanufacturing for Phase I clinical product is an asset.

Condition of employment

Reliability Status

For a Reliability Status, verification of…