Position: Quality Control Technician – Biopharmaceutical
Location: Saint-Laurent
Salary: Up to $60K, depending on experience

Do you have substantial experience in pipetting, handling enzymes, providing support for ELISA, and dealing with blood proteins? Do you possess experience in laboratory and quality control functions?
Our esteemed partner in the pharmaceutical and research sector, located in Saint-Laurent, is actively seeking a Quality Control Technician to join their dynamic team.
Seize the opportunity to apply your expertise and make a significant impact on groundbreaking research within a cutting-edge environment. Elevate your career to new heights by joining this team!
Don't miss your chance to be a part of something extraordinary. Apply now and embark on a journey of innovation and discovery!
Our client offers:
- 100% benefits paid by employer
- Holiday period 2 weeks of vacation + an additional 2 weeks of vacation
- 6 personal days
- Group RRSP with contribution of 6.5%
Our client is looking for you:


- Fluently bilingual as written documentation is provided from outside Quebec
- Minimum requirement of a DEC in the relevant scientific field
- 2 years of laboratory experience, with a minimum of 1 year in Quality Control functions
- Proficient pipetting skills
- Familiarity with various software applications, including MS Excel, MS Word, MS Outlook, statistical software, and graphical software
- ELISA (asset)

Your role:
- Manage raw materials essential for QC procedures
- Prepare required reagents and labels, and conducts sample analyses following SOPs for diagnostic and research enzyme production
- Validate analytical reports, ensuring timely documentation in adherence to the company's documentation practices
- Conduct stability studies, performs various tests (HPLC, protein, enzymatic activity assays, ELISA), and contributes to the assembly of ELISA kits
- Participate in the maintenance and calibration of pipettes and lab equipment, reviews documentation, and drafts quality control-related documents
- Facilitate purchasing and receiving of QC chemicals, oversee raw material releases, and ensures readiness for inspections and safety audits
- Contribute to monthly report drafting, aids in deviation investigations, and supports continuous improvement of analytical methods

Please send your resume to Cristina Bilbao at cristina.bilbao@quantum.ca.

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