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.

Robust 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@ 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

📌 Bio Analyst (Baie-D'Urfe)
🏢 ITR Laboratories Canada
📍 Baie-D'Urfe