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Manufacturing Technologist, Downstream

Job in Montreal, Montréal, Province de Québec, G4F, Canada
Listing for: Centre de production de produits biologiques (CPPB) inc. / Biologics Manufacturing Centre (BMC) Inc.
Full Time position
Listed on 2026-10-17
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Manufacturing & Industrial Operations, Manufacturing Engineer, Chemical Manufacturing
Salary/Wage Range or Industry Benchmark: 65000 - 90000 CAD Yearly CAD 65000.00 90000.00 YEAR
Job Description & How to Apply Below
Location: Montreal

The Biologics Manufacturing Centre (BMC) Inc.is a new biomanufacturing facility established in response to the pandemic. As a not-for-profit organization, BMC aims to better meet the biopharmaceutical needs of Canadians. BMC supports projects of public interest, actively contributes to the growth and resilience of Canada’s life sciences sector, and fosters industry development and innovation through Canadian manufacturing.

Driven by a team of engaged and innovative employees, BMC promotes a culture of agility and transparency through a collaborative, results-oriented approach.

We are currently seeking a Manufacturing
Technologist to join our Downstream team. At the heart of manufacturing operations, the successful candidate will be part of a highly technical team responsible for preparing, executing, and documenting purification activities for biological products and vaccines.

The Manufacturing
Technologist, Downstream will be responsible for:

  • Performing large-scale purification activities in compliance with client process requirements;
  • Operating specialized equipment, including chromatography columns and AKTA Ready, AKTA Readyflux, and Unicorn software interfaces;
  • Performing calibration, performance verification, and troubleshooting of equipment and instruments to ensure reliability;
  • Actively participating in GMP (Good Manufacturing Practices) training, including SOPs and manufacturing procedures;
  • Contributing to the drafting of Standard Operating Procedures (SOPs) and ensuring the accurate collection and recording of data in the appropriate documentation;
  • Assisting in the coordination and preparation of logbooks, batch manufacturing records, and client reports;
  • Performing GMP-compliant sampling, providing required samples, and conducting environmental monitoring activities;
  • Promoting and adhering to all applicable health and safety standards;
  • Performing and documenting the cleaning of manufacturing areas in accordance with established procedures.

The Biologics Manufacturing Centre (BMC) Inc.is a new biomanufacturing facility established in response to the pandemic. As a not-for-profit organization, BMC aims to better meet the biopharmaceutical needs of Canadians. BMC supports projects of public interest, actively contributes to the growth and resilience of Canada’s life sciences sector, and fosters industry development and innovation through Canadian manufacturing.

Driven by a team of engaged and innovative employees, BMC promotes a culture of agility and transparency through a collaborative, results-oriented approach.

We are currently seeking a Manufacturing
Technologist to join our Downstream team. At the heart of manufacturing operations, the successful candidate will be part of a highly technical team responsible for preparing, executing, and documenting purification activities for biological products and vaccines.

The Manufacturing
Technologist, Downstream will be responsible for:

  • Performing large-scale purification activities in compliance with client process requirements;
  • Operating specialized equipment, including chromatography columns and AKTA Ready, AKTA Readyflux, and Unicorn software interfaces;
  • Performing calibration, performance verification, and troubleshooting of equipment and instruments to ensure reliability;
  • Actively participating in GMP (Good Manufacturing Practices) training, including SOPs and manufacturing procedures;
  • Contributing to the drafting of Standard Operating Procedures (SOPs) and ensuring the accurate collection and recording of data in the appropriate documentation;
  • Assisting in the coordination and preparation of logbooks, batch manufacturing records, and client reports;
  • Performing GMP-compliant sampling, providing required samples, and conducting environmental monitoring activities;
  • Promoting and adhering to all applicable health and safety standards;
  • Performing and documenting the cleaning of manufacturing areas in accordance with established procedures.
Is this opportunity aligned with your career aspirations?

We would like to hear from you if:
  • You hold at least a post-secondary diploma in a life sciences-related discipline;
  • You have a minimum of one (1) year of experience preparing, executing, and documenting manufacturing or laboratory activities in the biopharmaceutical or biotechnology industry;
    • An equivalent combination of relevant education and experience may be considered;
  • You have hands-on experience with purification processes, including chromatography, TFF (Tangential Flow Filtration), and…
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