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ITR Laboratories Canada
Quality Assurance SupervisorITR Laboratories Canada • Baie d'urfé, QC, CA
Quality Assurance Supervisor

Quality Assurance Supervisor

ITR Laboratories Canada • Baie d'urfé, QC, CA
9 days ago
Job type
  • Full-time
  • Permanent
Job description

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 environment, 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
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Quality Assurance Supervisor • Baie d'urfé, QC, CA

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