Quality Systems Specialist / Spécialiste, Systèmes Qualité

<div> <div data-turn-id-container="request-WEB:665bb032-8573-4cb1-b733-ebd24a95edd2-89" data-is-intersecting="true"> <section data-turn-id="request-WEB:665bb032-8573-4cb1-b733-ebd24a95edd2-89" data-turn-id-container="request-WEB:665bb032-8573-4cb1-b733-ebd24a95edd2-89" data-testid="conversation-turn-8" data-scroll-anchor="false" data-turn="assistant" dir="auto"> <div> <div data-conversation-screenshot-content=""> <div> <div data-message-author-role="assistant" data-message-id="1eaa1b21-1cae-432b-ab70-d8f6421e8ad4" data-message-model-slug="gpt-5-3-mini" data-turn-start-message="true" tabindex="0" dir="auto"> <div> <div> <p data-start="0" data-end="213"><strong>This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a&nbsp;Quality Systems Specialist / Spécialiste, Systèmes Qualité based in Canada.</strong></p> <p data-start="215" data-end="1101">This role plays a key part in ensuring the integrity, compliance, and continuous improvement of a regulated quality system within a fast-evolving clinical research environment. You will act as a guardian of quality processes, helping maintain GxP compliance while supporting audits, inspections, and vendor oversight activities. The position combines operational QA execution with cross-functional collaboration across quality, regulatory, and vendor management teams. You will be responsible for driving inspection readiness, strengthening documentation standards, and ensuring effective CAPA management. In addition to core quality system activities, you will contribute to process improvements and training initiatives that enhance overall quality maturity. This is a highly collaborative role where your work directly supports compliance, patient safety, and operational excellence.</p> </div> </div> </div> </div> </div> </div> </section> </div> </div>