Bio Analyst

Bioanalyst Requisition Number: 20260713 Position Details Job Title: Bioanalyst Reports To: Manager Analytical Laboratories & Senior Director Analytical Work Category: Full-Time, Permanent Salary: Based on Experience Location: Baie-D'Urfé, Quebec 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. * Ability to manage multiple priorities and work effectively in a fast-paced laboratory environment. * Strong interpersonal and communication skills with the ability to work both independently and collaboratively. * Commitment to scientific excellence, continuous improvement, and regulatory compliance. Language Requirements * Fluency in French is required for internal communication. * Strong reading and writing skills in English are mandatory, as all study documentation is produced in English. What We Offer · Full-time permanent position (37.5 hours per week) * Competitive salary based on experience * Collective Health and Dental Insurance Plan * RRSP Contribution Program * Two (2) weeks of vacation * Opportunities for professional growth and continuous learning * Collaborative and supportive team environment * The opportunity to contribute to the development of new medicines that improve lives worldwide How to Apply Interested candidates are invited to submit their resume and cover letter to: HR@itrlab.com We thank all applicants for their interest in ITR Laboratories Canada Inc.; however, only those selected for an interview will be contacted. ITR Laboratories Canada Inc. is committed to providing equal employment opportunities and fostering an inclusive workplace. Monday to Friday: 8:30-16:45

The Bioanalyst performs bioanalytical testing on biological samples to evaluate drug concentrations and biomarkers in a GLP-regulated environment. Responsibilities include sample preparation, operating analytical instrumentation, and ensuring strict adherence to SOPs and regulatory requirements.

A Bachelor's degree in Biochemistry, Chemistry, or a related scientific field is required, with a Master's degree preferred. Candidates should have knowledge of GLP/GDP and experience with analytical techniques like LC-MS/MS or HPLC.

• Collective Health Insurance • Dental Insurance • RRSP Contribution Program • Two Weeks Of Vacation • Professional Growth Opportunities

• Data analysisPreferred

Identified from the job description. Confirm important requirements above.

• LC-MS/MS
• HPLC
• ELISA
• Sample Preparation
• GLP
• GDP
• Data Analysis
• Method Validation
• Bioanalytical Testing
• Laboratory Instrumentation
• Quality Control
• Regulatory Compliance

• Science & Research
• Healthcare
• Manufacturing

Minimum education

Bachelor’s degree

Minimum experience

2+ years

Posting language

English

Working hours

38 hours per week