Medical Laboratory Technologist

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

Perform and validate clinical and research-based laboratory analyses across various disciplines including molecular biology and hematology. Ensure strict adherence to quality standards such as ISO 15189, GLP, and GCP to deliver precise diagnostic results.

Requires a DEC in Biomedical Laboratory Technology and an active OPTMQ membership. Candidates must have 3-5 years of experience in medical laboratory environments and proficiency in PCR technologies.

• Health Insurance • Dental Insurance • Vision Insurance • RRSP Participation Plan • Paid Vacation • Sick Days • Professional Development • Technical Training

• Quality assurancePreferred

Identified from the job description. Confirm important requirements above.

• Clinical Laboratory Analysis
• Molecular Biology
• qPCR
• RT-PCR
• ddPCR
• DNA/RNA Extraction
• ISO 15189
• Quality Assurance
• Hematology
• Biochemistry
• Urinalysis
• Toxicology
• Cytology
• Immunology
• Microscopy
• Sample Validation

• Healthcare
• Science & Research

Minimum education

College diploma

Minimum experience

2+ years

Apply by

Sep 16, 2026

Posting language

English

Working hours

38 hours per week

Seniority

Associate

Application method

Direct apply is available