We are seeking a skilled Lab Technician with hands-on experience in chromatography to join our pharmaceutical manufacturing team.

• Hands-on experience with HPLC systems.
• Knowledge and practical laboratory experience in chemical and physical analysis of pharmaceutical products.
• Ability to work independently, accurately, and meticulously with minimal supervision.
• Good written and verbal communication skills in both French and English to ensure clear documentation for international audits.
• DEC diploma in Biopharmaceutical Production Technology or a related scientific field.

• Use of computerized systems for data generation, compilation, and review.
• Data documentation and reporting according to SOPs and QA requirements.
• Problem-solving: investigating testing deviations and implementing corrective/preventive actions.

• Perform chromatographic, chemical, and physical testing/analysis of incoming raw materials, in-process samples, finished products, stability samples, rinse water, pharmaceutical water systems, and environmental monitoring samples in accordance with SOPs, cGMP, and regulatory guidelines.
• Operate, calibrate, and maintain a variety of laboratory instruments, including UHPLC.
• Perform documentation and reporting in compliance with SOPs and QA requirements. Maintain laboratory records and primary data in accordance with applicable regulations and company policies.
• When required, coordinate testing activities with QA and Production/Manufacturing teams to provide timely analytical results and ensure continuous process flow and compliance with specifications.
• Prepare reagents and buffers for QC and R&D activities.
• Maintain documentation, equipment history records, and test methods to ensure compliance. Perform laboratory housekeeping and manage laboratory supplies to maintain adequate inventory levels and prevent testing delays.
• Use computerized systems for data generation, compilation, and review.
• Investigate testing deviations or abnormalities and implement corrective and preventive actions as required.
• Assist with special R&D projects as required.
• Perform other related duties as assigned by the Supervisor.

• Over three years of HPLC/UHPLC experience is considered an asset.
• Knowledge of cGMP regulations is an asset.

Employment Type: Full-time – Maternity Leave Replacement (with possibility of permanent employment) Start Date: Immediately Working hours: 8:00 a.m. to 4:30 p.m., from Monday to Friday.