ROLE AND RESPONSIBILITIES
Reporting to the Manager, Projects and Compliance, you coordinate projects and all activities related to good manufacturing practices. Based on the quality indicators, you ensure service compliance when changes are made to processes and equipment. You participate in drafting and tracking changes to all regulatory documents, as well as assessing the impacts on validation, work methods and risks related to changes. You are also involved in the investigation process when quality issues arise, as well as in process improvement.
More specifically, you:
Available to travel to the various Héma-Québec facilities, GLOBULE Blood Donor Centres and PLASMAVIE Plasma Donor Lounges