Bio Analyst

ITR Laboratoires Canada Inc•Baie-D'Urfé, QC

8d•Onsite

About The Position

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.

Requirements

B.Sc. in Biochemistry, Chemistry, Analytical Chemistry, Biotechnology, Pharmaceutical Sciences, Biology, or a related scientific discipline.
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.
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.

Nice To Haves

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.

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.