Bio Analyst

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@

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