Responsibilities Supervise, coach, and support Quality Assurance personnel.

Coordinate inspections, audits, and QA activities to ensure timelines are met.

Conduct and oversee quality inspections, audits, and compliance assessments.

Support Sponsor, Regulatory Authority, and third-party inspections.

Manage and maintain Quality Management Systems, SOPs, CAPA programs, deviation management, and document control systems.

Support validation and qualification activities for facilities, equipment and computerized systems, Deliver and coordinate QA-related training programs.

Collaborate with cross-functional departments to promote quality and continuous improvement initiatives.

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 Bachelor''s Degree in Life Sciences, Biological Sciences, Pharmaceutical Sciences, Quality Management, or a related field.

Minimum 7 years of Quality Assurance experience in a preclinical regulated workplace, involving laboratory animal models.

Experience in quality auditing, quality systems management, validation, CAPA management, and regulatory inspections.

Experience supporting client, sponsor, and regulatory audits and inspections.

Strong coaching, mentoring, and training skills.





Experience in biotechnology, toxicology, safety pharmacology research environments.

Strong knowledge of: FDA 21 CFR Part 58 and Part 11 OECD Good Laboratory Practice (GLP) Skills and Competencies Strong leadership and team management skills.

Excellent auditing, inspection, and problem-solving abilities.

Effective communication, training, and report-writing skills.

Ability to manage multiple priorities in a fast-paced environment.

Proficiency with Microsoft Office applications.

Ability to work effectively with diverse teams and stakeholders.

Language Requirements Strong reading and writing skills in English are mandatory, as all study documentation is produced in English.

Fluency in French is required for internal communication.

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 $36.00/hr

📌 Quality Assurance Supervisor (Baie-D'Urfe)
🏢 ITR Laboratories Canada
📍 Baie-D'Urfe