Quality Specialist

The Quality Specialist will assist in the development, implementation, maintenance and evaluation of the HRLMP Quality Management System to meet patient, client and regulatory requirements. Responsibilities include: facilitates quality improvement projects using quality tools and standard methodology, development and coordination of Standard Operating Procedures, coordination of internal audits, supports activities for internal audits and external audits such as Accreditation Canada - Diagnostics, monitors non-conformances, occurrence reporting, corrective/preventive actions and coordinates the collection and analysis of data for improvement opportunities. Development and coordination of applications for Paradigm3 Business Management Software. Coordinates and assists in the development and data analysis of client satisfaction surveys, collaborates to create mechanisms to capture data for key indicators within the LIS and Quality System Software, supports specific activities or projects within the Quality System development, implementation and maintenance. 1. Advanced Registered Technologist or BSc in a related science or Bachelor of Technology 2. Current Registration with the College of Medical Laboratory Technologist of Ontario (CMLTO) 3. Demonstrated experience in Clinical Laboratory Medicine operations 4. Demonstrated strong leadership, organization and facilitation skills, customer service orientation, problem solving and project management skills 5. Demonstrated experience in the application of integrated computer systems software 6. Demonstrated knowledge and experience in Quality Management Systems 7. Demonstrated excellence in communication (written and verbal), interpersonal skills, team building, and the ability to initiate and model positive change 8. Knowledge of Laboratory Standards and Regulations 9. Proficiency in Microsoft Office 10. Recognized Academic qualifications in either, Quality Management, Business Management, Health Management or Project Management would be an asset

The Quality Specialist will manage the Quality Management System, including coordinating audits, non-conformances, and corrective actions. They will also facilitate quality improvement projects and develop Standard Operating Procedures to ensure compliance with regulatory requirements.

Candidates must hold an Advanced Registered Technologist status or a Bachelor's degree in a related science or technology field. Current registration with the CMLTO and demonstrated experience in clinical laboratory operations are required.

• Service à la clientèleSouhaitée
• Résolution de problèmesSouhaitée
• LeadershipSouhaitée
• Analyse de donnéesSouhaitée
• CommunicationSouhaitée
• Microsoft OfficeSouhaitée
• Gestion de projetSouhaitée

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

• Quality Management Systems
• Clinical Laboratory Medicine
• Standard Operating Procedures
• Internal Audits
• Data Analysis
• Project Management
• Leadership
• Facilitation
• Customer Service
• Problem Solving
• Microsoft Office
• Laboratory Standards
• Regulatory Compliance
• Team Building
• Communication
• Quality Improvement
• Auditing
• Management
• Corrective And Preventive Action (CAPA)
• Medical Laboratory
• External Auditing
• Standard Operating Procedure
• Interpersonal Communications
• Operations
• Quality Management
• Registered Technologist
• Coordinating

• Healthcare
• Science & Research
• Management & Leadership
• Administrative
• Quality Specialist
• Quality Assurance Specialist
• Product Graders and Testers (except Foods and Beverages)
• Inspectors, Testers, Sorters, Samplers, and Weighers

Formation minimale

Baccalauréat

Expérience minimale

5+ ans

Postuler avant le

11 août 2026

Langue de l’offre

anglais

Heures de travail

40 heures par semaine