About the job

Medical Laboratory Technologist

Location: 4868 Rue Levy Suite 210, Saint-Laurent, QC H4R 2P1

Type: Full-time, On-site, Monday to Friday

About Famililab Canada

Famililab.care is a healthcare organization dedicated to advancing personalized, patient-centered care through innovation, technology, and scientific excellence.

Our Integrated Care Center (ICC) and Diagnostic Laboratory bridge clinical care and translational research, ensuring compliant, high-quality operations that contribute to evidence-driven healthcare.

Our Mission

At Famililab, we believe that research and diagnostics should directly enhance patient care.

Join us in advancing precision medicine, quality standards, and the future of value-based healthcare.

Position Overview

The Medical Laboratory Technologist performs and validates clinical and research-based laboratory analyses under the supervision of the Director of Laboratory Diagnostics & Method Development.

This role ensures adherence to GLP, CAP, GCP, CLSI standards, LSPQ & OPTMQ guidelines, and ISO 15189 quality management requirements as well as Health and Safety guidelines, while supporting Famililab’s mission to deliver precise, reliable, and clinically meaningful results.

Core Laboratory & Molecular Biology Laboratory Duties

• Process and analyze patient samples using automated and manual methodologies.
• Conduct testing in core laboratory such as but not limited to; hematology, coagulation, biochemistry, urinalysis, toxicology, cytology, immunology, molecular biology and microscopy.
• Validate, record, and report results in accordance with Standard Operating Procedures (SOPs).
• Maintain traceability, data integrity, and sample documentation.
• Support assay development and validation initiatives.
• Perform DNA and RNA extraction, amplification, and molecular analysis using PCR technologies (qPCR, RT-PCR) for the molecular biology laboratory.
• Execute molecular assays in compliance with national and international standards.
• Ensure contamination control, and accurate reporting.
• Perform other laboratory related work as requested by the director of the laboratory.

Quality Assurance & Compliance

• Adhere to GCP, GLP, OPTMQ, CAP, ISO 15189, CLSI, and LSPQ standards always.
• Participate in quality control programs, instrument calibration test verification, internal audits and proficiency testing.
• Document and assist in corrective actions and non-conformity investigations.
• Support SOP validation, analytical method review, and continuous improvement initiatives.

Qualifications

Required Qualifications

• DEC in Biomedical Laboratory Technology
• Active OPTMQ membership
• Proficiency in clinical and molecular laboratory techniques (qPCR, RT-PCR, ddPCR)
• Minimum 3–5 years of experience in medical laboratory environments (diagnostic or research)
• Strong analytical and troubleshooting abilities
• Demonstrated knowledge of ISO 15189 standards
• Self-directed and organized, with the ability to work both independently and collaboratively
• Computer literacy and strong documentation skills
• Excellent verbal and written communication skills in English and French

Preferred Assets

• Familiarity with laboratory automation systems and Laboratory Information Systems (LIS/LIMS)
• Prior participation in accreditation or quality audit processes
• GCP and/or GLP certification
• Laboratory Biosafety experience

Work Schedule

Full-time, on-site position

Standard working hours: Monday to Friday, 7:30 a.m. to 3:30 p.m. (37.5 hours per week)

Occasional flexibility may be required to support operational needs, quality activities, or special laboratory projects.

Compensation & Benefits

• Hourly Rate: $27.71 – $39.88 (based on experience and qualifications) / 37.5 hours/week
• Comprehensive benefits package health, dental & vision
• RRSP participation plan
• Paid vacation and sick days
• Ongoing professional development and technical training opportunities