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Bio Analyst

Job in Quebec, Québec, Province de Québec, Canada
Listing for: ITR Laboratories Canada Inc.
Full Time position
Listed on 2026-07-18
Job specializations:
  • Research/Development
    Medical Technologist & Lab Technician, Clinical Research, Data Scientist
  • Healthcare
    Medical Technologist & Lab Technician, Clinical Research, Data Scientist
Salary/Wage Range or Industry Benchmark: 65000 - 90000 CAD Yearly CAD 65000.00 90000.00 YEAR
Job Description & How to Apply Below
Location: Quebec

Reports To: Manager Analytical Laboratories & Senior Director Analytical

Work Category: Full-Time, Permanent

Salary: Based on Experience

About ITR Laboratories Canada Inc.

At ITR Laboratories Canada Inc., our mission is to bring new medicines to the world and help improve the health and well-being of individuals across the globe. For over 35 years, ITR has been a trusted partner to the pharmaceutical and biotechnology industries, providing high-quality drug safety assessment services that support the development of innovative therapies. Our commitment to scientific excellence, animal welfare, regulatory compliance, and continuous improvement makes ITR a recognized leader in preclinical research services worldwide.

Position

Summary

The Bioanalyst plays a key role in supporting preclinical and pharmaceutical research by performing bioanalytical testing on biological samples to evaluate the concentration of drugs, metabolites, and biomarkers. Working in a GLP-regulated environment, the Bioanalyst is responsible for sample preparation, method execution, operation of analytical instrumentation, data review, and documentation activities. This position contributes to the generation of high-quality scientific data while ensuring compliance with study plans, Standard Operating Procedures (SOPs), Good Laboratory Practices (GLP), and regulatory requirements.

The ideal candidate is detail-oriented, scientifically curious, and committed to maintaining the highest standards of data integrity and laboratory excellence.

Key Responsibilities
  • Perform bioanalytical sample preparation procedures, including extraction, dilution, and processing of biological matrices such as plasma, serum, urine, and tissues.
  • Conduct quantitative and qualitative analyses using analytical instrumentation, including LC-MS/MS, HPLC, ELISA, or other laboratory platforms as applicable.
  • Operate, maintain, troubleshoot, and document the performance of laboratory equipment and analytical instruments.
  • Review study plans, analytical procedures, SOPs, and protocols to ensure accurate execution of assigned activities.
  • Prepare reagents, calibration standards, quality control samples, and laboratory solutions required for bioanalytical testing.
  • Accurately record observations, analytical results, and raw data in accordance with GLP, SOPs, and regulatory requirements.
  • Review analytical data for accuracy, completeness, and compliance with study requirements.
  • Identify, document, and promptly report deviations, out-of-specification results, equipment issues, or unforeseen events to management.
  • Participate in method qualification, validation, transfer, and improvement activities.
  • Assist with sample receipt, storage, tracking, inventory management, and chain-of-custody documentation.
  • Support laboratory inspections, audits, and regulatory submissions through accurate documentation and record maintenance.
  • Maintain a clean, safe, and organized laboratory environment while adhering to all health and safety procedures.
  • Collaborate with Study Directors, Scientists, Principal Investigators, and laboratory staff to ensure study timelines and objectives are achieved.
  • Participate in training activities and contribute to continuous improvement initiatives within the Bioanalytical Services Department.
Required Qualifications
  • B.Sc. in Biochemistry, Chemistry, Analytical Chemistry, Biotechnology, Pharmaceutical Sciences, Biology, or a related scientific discipline.
  • M.Sc. in a related field is considered an asset.
  • Experience in a bioanalytical, pharmaceutical, biotechnology, CRO, or regulated laboratory environment is considered an asset.
  • Hands-on experience with analytical techniques such as LC-MS/MS, HPLC, or similar technologies is preferred.
  • Knowledge of Good Laboratory Practices (GLP), Good Documentation Practices (GDP), and regulatory requirements.
  • Strong understanding of scientific principles, data analysis, and analytical laboratory procedures.
  • Proficiency with laboratory software, data acquisition systems, and Microsoft Office applications.
  • Excellent attention to detail and commitment to data quality and integrity.
  • Strong organizational, analytical, and problem-solving abilities.
  • Abi…
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