Responsibilities Process biological samples by centrifuging whole blood and separating plasma and serum according to study protocols.

Accurately record observations, raw data, and laboratory activities in compliance with GLP, SOPs, and study requirements.

Read, understand, and follow study plans, SOPs, and GLP requirements; participate in pre-study meetings when required.

Prepare laboratory materials, reagents, solutions, and supplies required for pharmacokinetic studies.

Operate, maintain, troubleshoot, and support validation activities for laboratory equipment to ensure reliable performance.

Promptly report unforeseen events, deviations, equipment issues, or study-related concerns to the Senior Section Leader, Senior Manager, and Study Director.

Maintain accurate inventory records and traceability of PK samples throughout study execution.

Review, organize, and prepare PK samples for domestic and international shipment.

Prepare, renew, and maintain CITES permit applications and related documentation for biological sample shipments.

Ensure valid and current CITES permits are available when required to support study timelines and shipment schedules.

Contribute to laboratory organization, housekeeping, and the maintenance of a secure and compliant work environment.

Perform other related duties and departmental tasks as assigned Required Qualifications D.E.C. in Medical Laboratory Technology or a related scientific field.

Equivalent education and relevant laboratory experience may be considered.





Experience handling and processing biological samples is considered an asset.

Knowledge of Good Laboratory Practices (GLP) and Standard Operating Procedures (SOPs).

Experience with laboratory equipment operation, maintenance, and validation is an asset.

Strong attention to detail and commitment to data integrity and quality.

Excellent organizational and record-keeping skills.

Ability to work independently and collaboratively in a fast-paced laboratory environment.

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 Market-competitive salary based on experience Full-time permanent position (37.5 hours per week) 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 current 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.

Evening/Night Shift

📌 PK Technician (Baie-D'Urfe)
🏢 ITR Laboratories Canada
📍 Baie-D'Urfe