Analyst Quality Control, Microbiology - Montréal, Canada - Centre de production de produits biologiques (CPPB) Inc. / Biologics Manufacturing Centre (BMC) Inc.

Centre de production de produits biologiques (CPPB) Inc. / Biologics Manufacturing Centre (BMC) Inc.
Centre de production de produits biologiques (CPPB) Inc. / Biologics Manufacturing Centre (BMC) Inc.
Verified Company
Montréal, Canada

3 weeks ago

Sophia Lee

Posted by:

Sophia Lee

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Description
The Biologics Manufacturing Centre (BMC) Inc. is a 54,900 square foot biomanufacturing facility whose construction was completed in June 2021.

The BMC supports the expansion of the country's biologics manufacturing capacity, ensuring that vaccines and other related products can be safely manufactured at home.

BMC is designed to create biopharmaceuticals such as viral vector, protein subunit and virus-like particle vaccines and other biologics.

In order to contribute to the implementation of the new not-for-profit organization and to make biomedical innovations more accessible to Canadians, we are looking for a

Analyst

Quality Control, Microbiology
***who will support the activities of the quality control department, microbiology. This is a temporary position, to replace a 12-month maternity leave. Position start planned for Septembre, 2023.

Under the supervision of the Supervisor quality control, microbiology, the
-
Analyst

Quality Control, Microbiology
***will be responsible for:

  • Perform environmental monitoring (viable/nonviable air and water sampling)
  • Execute inprocess and finished product testing (bacterial endotoxin, bioburden, microbial identification)
  • Support in the management of inventory of quality control consumables
  • Support in investigations of out of specification (OOS)/ out of tendance (OOT) results
  • Support to production team
  • Improve QC activities
  • Contribute to the maintenance and calibration of quality control equipment
  • Contribute to writing SOPs for microbiological testing based on compendial tests
  • Contribute to method validation protocol writing and execution

You are the person we are looking for if:

  • You hold at least a College Diploma (DEC) in a scientific discipline related to microbiology
  • You have at least one (1) year of work experience in the field of pharmaceuticals in quality control laboratory, and in air sampling, water sampling in an environment respecting Good Manufacturing Practices (GMP)
  • A combination of relevant education and experience may be considered
  • You have knowledge of equipment maintenance and troubleshooting, and of working in ascetic conditions
  • The following experiences are assets: analysis of inprocess and finished product and raw materials (bioburden by membrane filtration, LAL turbidimetric/chromogenic, etc.); and sterile manufacturing
  • You are customeroriented, have a good collaboration spirit and a great sense of organization and priority management
  • Flexible schedule and overtime may be occasionally required including evenings, nights, weekends, and holidays

What we offer:


  • A respectful and friendly work environment in a new facility with stateoftheart equipment
  • A competitive salary commensurate with your skills
  • Onsite parking
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